Scientific Manager Resume Samples

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C Emmerich

Claudia

Emmerich

2702 McDermott Oval

New York

+1 (555) 490 3197

2702 McDermott Oval

New York

Phone

p +1 (555) 490 3197

Experience Experience

Dallas, TX

Scientific Affairs Manager

Dallas, TX

Ullrich, Schuster and Conn

Dallas, TX

Scientific Affairs Manager

Ensures the organization complies with all relevant policies and procedures to ensure the Quality objectives of the business are met. Comply with all relevant company Occupational Health, Safety and Environmental policies, procedures and work practices with the intent of preventing or minimizing accidental exposures to self, colleagues and/or the environment
Coordinate continuing education workshops, seminars, and training programs for graduate physicians, scientists and health and medical personnel. Conceptualize, organize and analyze data, interprets, and synthesize complex clinical and non-clinical statistical reports to derive key outcomes and messages. Translate scientific and technical issues for diverse audiences
Contributes to the development of the clinical evidence in collaboration with the Clinical and Marketing teams, including early beta testing for all product launches in the region
Represents the company to groups of experts including Medical Professionals, societies, and Regulatory at Scientific Meetings
Develops and implements scientific studies and drives an aggressive publication plan in North America through developing and managing key thought leader engagement
Responsible for implementing and maintaining the effectiveness of the APOC quality system
Collaborates with product management, downstream marketing, clinical and regulatory affairs as well as commercial teams in multiple areas including publication planning, speaker education programs, regional consultant meetings, manuscript review and conference and local meetings preparation

New York, NY

Senior Scientific Manager

New York, NY

Schamberger-Batz

New York, NY

Senior Scientific Manager

Support ODQ creation, and tracking
Actively engage/interact with key stakeholders, including
Global Medical Affairs Leadership
Coordinate Medical work stream/taskforces such as MRD initiatives, MoA story and slide finalization
Partner closely with Scientific communications and Medical Information
Directly support GMA MM directors in creating tools and materials such as PowerPoint slide decks to support Medical activities related to Rev and Pom G3M teams as well as materials for external use
Provide support in mapping Medical MM activity timelines, develop & update plans such as Medical Education overviews, KOL engagement plans, cooperative group strategy representation, Ad board planning

present

Chicago, IL

Senior Scientific Affairs Manager

Chicago, IL

Auer-Hand

present

Chicago, IL

Senior Scientific Affairs Manager

present

Coordinates continuing education workshops, seminars, and training programs for graduate physicians, pharmacists, scientists and health and medical personnel. Conceptualize, organize and analyze data, interpret, and synthesize complex clinical and non-clinical statistical reports to derive key outcomes and messages. Translate scientific and technical issues for diverse audiences
Act as high level resource for customers, sales and marketing. Address customer’s scientific inquiries (on-label and off-label unsolicited requests), documents requests and actions, supports customer scientific and clinical applications
Liaise with Global Medical and Scientific Affairs, product development, marketing, sales and operations teams to scientifically support commercialization of Roche products (e.g. scientific and clinical content development, etc.). Acts as single point of contact between Roche and advisers
Develop strategies and priorities for clinical studies that support existing products and new products in development
Support molecular materials for content review and management in VEEVA
Collaborate with global medical affairs and business colleagues to develop medical plans, identify gaps in current knowledge, and oversee study management of Investigator-Initiated and Roche-Sponsored Studies within the sequencing business area. Conduct briefings and collaborations with Roche technical and global partners
Provide critical review of scientific information and data, generating timely feedback and insight to Roche partners

Education Education

Bachelor’s Degree in Biomedical Sciences From

University of Illinois at Chicago

Bachelor’s Degree in Biomedical Sciences From

Skills Skills

Strong knowledge of molecular biology and skills in the analysis of human specimens
Ability to preside over meetings showing leadership qualities, independence with sound ideas, vision and ability to remain focused on the mission/project
Strong and proven technical skill and knowledge in genomics, molecular biological and genomic assay development
Attention to detail and ability to identify and successfully address unexpected results
Ability to work within a highly matrix team environment
Ability to deliver high quality results in a timely manner
Proven ability to manage projects and staff as well as work independently
Ability to write and orally present data and project updates in a clear and effective manner
Risk Management – ability to identify technical, budgetary, and schedule risks to the program and plan appropriate risk response strategies
Experience with diagnostic assay development

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15 Scientific Manager resume templates

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Manager, Scientific Affairs Resume Examples & Samples

Ensure the scientific substantiation of claims across select brands
Prepare the claim substantiation summary for final sign-off
Understand the brands’ business strategies
Establish innovative claim strategies in collaboration with Product Development and Marketing partners
Support corporate teams on scientific-related topics
Partner with Clinical, Consumer, Safety and BSR teams to establish and implement testing programs to support claims
Establish consistent claim substantiation documentation, in partnership with Legal, throughout global product registrations and more generally new product claim substantiation
Maintain the product claim section of the Product Information File
Assist internal partners on technical questions related to claims
Work with experts to provide supplementary claim support
Develop testing programs for new technologies, in collaboration with Clinical Testing, Consumer Science and Basic Sciences
Minimum of Master’s degree in a scientific discipline (Biology, Biophysics, Biochemistry, pharmacology or related fields). PhD preferred
Experienced claim substantiation professional having minimum of 5 years industry/business experience. Experience directly related to personal/cosmetic products is preferred
Requires at least 5 years R&D experience in the development of new personal care/cosmetic or consumer health products or technologies
Effective organizational planning skills and project management of multiple projects/products is required
Excellent analytical, written and verbal language skills with outstanding proficiency in English are necessary
Possess excellent judgment, tact, diplomacy and flexibility
Computer literate including MSWord, Microsoft Outlook, Excel, PowerPoint desirable
Proven Leadership, Communication and Collaboration skills
Requires experience in successfully interacting with external experts to help drive research programs, testing and identify future technology trends
Ideally has experience in the direct interaction with Marketing and Legal

Manager, Scientific Meetings Resume Examples & Samples

Bachelor's degree in business administration, program management, meeting management, or a related field
Minimum of three (3) years of experience managing the programming for conferences
Minimum three (3) years of experience planning and managing budgets
Ability to work independently and make appropriate, effective decisions related to project management responsibilities
Must possesses strong communication (written and verbal) and consensus-building skills
Skilled in Microsoft Office (Word, Excel, Power Point, Outlook)
Must be able to travel overnight up to 15% of the time
Previous experience working with volunteers in a not-for-profit environment preferred
Someone who has studied principles of adult education

Scientific Affairs Manager Resume Examples & Samples

Develop scientific and clinical evidence to support the DxN VERIS Molecular Diagnostics System and assays in USA and Canada
Assess scientific and medical data, formulates scientific plan strategy, and assists in development of customer responses and communication in technical areas
Contributes to the development of the clinical evidence in collaboration with the Clinical and Marketing teams, including early beta testing for all product launches in the region
Represents the company to groups of experts including Medical Professionals, societies, and Regulatory at Scientific Meetings
Develops and implements scientific studies and drives an aggressive publication plan in North America through developing and managing key thought leader engagement
Develops and leads plans with key opinion leaders, customers and others to define the gaps and potential requirements/needs for existing and future product offerings
Responsible for the development and execution of projects that will provide more extensive background, additional data or answers to questions in response to issues that arise relative to commercial, scientific or data needs
Regular communication with the external medical community to remain abreast of issues in the field and to provide medical support and direction to them
Collaborates with product management, downstream marketing, clinical and regulatory affairs as well as commercial teams in multiple areas including publication planning, speaker education programs, regional consultant meetings, manuscript review and conference and local meetings preparation
Attends most major conferences and helps coordinate medical affairs activities at conferences, including presenting to external audiences as needed
Manages projects to completion, anticipating obstacles and difficulties that may arise, resolving them in a collaborative manner
May perform other related duties as required and/or assigned
Ph.D. degree (molecular biology preferred)
Over 5 years of experience in similar roles, ideally in infectious disease and leading scientific affairs and marketing initiatives
Molecular IVD experience preferred (experience in clinical molecular diagnostics lab a plus)
Incumbent must have excellent communication skills as well as analytical, project management and planning skills. Public speaking experience a plus
Flexible, curious and tenacious with a can do positive approach in a start-up environment
Self-starter, able to work independently – strong team player. Cross-functional team leadership experience strongly preferred
Able to travel up to 60% in Canada and USA
Experience in development and oversight of scientific studies

Manager, Scientific Management Resume Examples & Samples

Manage and support analysis of large clinical biomarker datasets
Effectively manage scientific collaborations, both internal and external
Provide expert analytical support for Biomarker teams
Drive scientific and technical innovation collaboratively with other members of the Department
Support execution on lead and exploratory biomarker strategies for multiple projects
Support publications in high quality scientific, technical or medical journals
Represent the biomarker team externally through interactions with our key investigators
Participate and thrive in an interactive, team oriented culture

Manager, Scientific Affairs Resume Examples & Samples

Participates as a member of the Due Diligence (DD) team from kick-off through close-out, to evaluate target opportunities with a CMC sub-team, looking for risks and opportunities in the area of API and Finished Product characterization/evaluation and any other aspects based on QbD which could impact the successful development, filing and commercialization of the target asset
Prepares DD reports to summarize the findings into a concise evaluation of possible risks and opportunities, and a prioritized, actionable plan and mitigation strategy
Provides timely updates to the Scientific Affairs and BD&L leadership
8 years’ experience with Master’s degree or at least 6 year experience with PhD in formulation development preferred

Scientific Affairs Manager Resume Examples & Samples

Market and manage the Oncology products for the Region, driving the successful launch of new Oncology tests. Leading the development of the European Oncology markets to achieve budget for all associated products
Manage budget and forecast for associated products
Prepare and implement a European marketing plan for all associated products
Deliver monthly reports, and quarterly marketing plan updates
Develop and communicate key messages, value propositions, marketing programs, and sales tools for associated products
Train sales force on optimal usage of marketing and sales tools
Regularly travel with sales representatives on sales calls to understand customer issues and front line challenges to successful selling of associated products, coach on how to best implement and overcome challenges, develop sales tools and programs to address these needs. Provide feedback to sales and global marketing on visits
Develop and maintain an excellent relationship with Cepheid global and country marketing teams as well as Distributors, coordinating activities with all key stakeholders
Ensure there is a high level of awareness of market developments, government policies, competitor activities and customer’s needs
Promotes meetings and initiatives with Key Opinion Leaders, taking opportunities for leveraging the Product Portfolio
Work on Distribution Channel Strategies
Incumbent must have a proven track record that clearly demonstrates success in positions with increasing levels of responsibility
Experience in specific disease area (bladder or breast priority) and knowledge of real time PCR reagents and instruments is desired
High degree of leadership and able to engage with and successfully influence others including colleagues and customers, ranging from lab technicians to clinical experts
Because of the technical nature of the products, an understanding of the assigned products and their relationship to diagnostic and clinical medicine is essential. Incumbent must possess a high degree of sensitivity and maintain close contact with the marketplace to determine those areas where new clinical diagnostic products with improvements are required
Minimum MD or PhD in clinical pathology, molecular biology or related field
Minimum 5 years' experience as experience in scientific/medical affair or marketing experience
Experience at the Laboratory manager level preferred
Must be experienced in developing and delivering Powerpoint presentations on clinical topics to laboratories and clinicians

Senior Scientific Manager Resume Examples & Samples

Directly support GMA MM directors in creating tools and materials such as PowerPoint slide decks to support Medical activities related to Rev and Pom G3M teams as well as materials for external use
Provide support in mapping Medical MM activity timelines, develop & update plans such as Medical Education overviews, KOL engagement plans, cooperative group strategy representation, Ad board planning
Ensure efficient coordination of tools & materials development across functions and geographies (identify synergies while eliminating duplications), consider bringing agency work in-house where applicable and partner closely with outside agencies where useful and cost-effective
Support ODQ creation, and tracking
May provide support to preparation of materials required for Advisory boards
Coordinate Medical work stream/taskforces such as MRD initiatives, MoA story and slide finalization
Contribute to appropriate presentations of MM Medical metrics such as MM IIT status updates into Medical presentations; as such closely partner with GMA strategic planning and operations
Partner closely with Scientific communications and Medical Information
Under guidance of Scientific directors, extract MM specific information from other sources, ie Med Info, and present in graphical and analytical ways
Actively engage/interact with key stakeholders, including
Med Affairs partners in disease area
Global Medical Affairs Leadership
Market Access
Clinical
BioStats
Translational
Expertise and previous experience in project management roles
Bachelor’s degree required, advanced degree (Master’s, Doctorate is a plus) in health-related field is preferred. Expertise in hematology/oncology including relevant content area, with 3-5 years industry experience
Medical Affairs experience and knowledge in the interpretation of clinical trials data in hematology/oncology is a plus
Previous roles as CRS or SM (study manager) can be considered
Communications background is a plus
Experience in the conduct of clinical trials in hematology/oncology preferred including biostatistics knowledge
Scientific mindset and interest in improving patient treatment options & outcomes
Proven track record of project management skills
Excellent analytical and synthesis concluding skills
Skilled in creating presentations; strong visual graphics skills, proficient with relevant IT programs
Used to work in cross functional, matrix teams
Summit, NJ based position, limited travel required (<20%)

Scientific Manager Resume Examples & Samples

Ph.D. in biomedical sciences (preference immunology) from an accredited college/university according to the Council for Higher Education Accreditation (CHEA)
Possession of a Doctoral degree in biomedical sciences from an accredited college or university according to the Council for Higher Education Accreditation (CHEA) appropriate to biomedical research
A minimum of eight years of post-graduate experience including five or more years of managerial experience
Strong knowledge and experience in vaccine development
Strong knowledge of T-cell immunology, vaccines and adjuvants
Experience in preclinical research using different mouse models
Experience in assay development and validation
Outstanding record keeping abilities
Record of first-author publications
Scientific writing and presentation skills
Leadership skills with ability to train and lead others
Manage communications with internal and external collaborators, project milestones and timelines
Excellent problem solving and troubleshooting skills
Experience in preclinical research and assay development in the area of vaccines/biologics
Experience in GLP environment and understanding of regulatory requirements for vaccine development

Scientific Affairs Manager Resume Examples & Samples

Provides strategic clinical direction and consultation to all aspects of product commercialization, including product performance, customer communications, and scientific marketing
Provides scientific support in the resolution of product issues and promotion of APOC products
Represents APOC in meetings with key customers, government agencies, and scientific/professional organizations
Responsible for implementing and maintaining the effectiveness of the APOC quality system
Stays current with literature in field; provides technical assessment and utility of key publications to sales and marketing staff. Prepares and delivers technical training internal and external customers
Assists marketing & sales in handling and overcoming product objections
Identifies speakers and develops scientific programs to support marketing workshops & symposia. Identifies and develops good relationships with KOLs. Participates actively in congresses
Defines objectives and expectations for product evaluations and works with investigators to develop protocol. Assists the development of publication or in-house report and ensures final publication or distribution/presentation
Drive regulatory & clinical strategies in alignment with company business goals ensuring timely registration of all new products for market growth and renewal of expiring product licenses for business continuity
Ensures the organization complies with all relevant policies and procedures to ensure the Quality objectives of the business are met. Comply with all relevant company Occupational Health, Safety and Environmental policies, procedures and work practices with the intent of preventing or minimizing accidental exposures to self, colleagues and/or the environment
The position is accountable for the scientific strategy/direction of the affiliate including advocacy & product commercialization (product performance, customer communications, and scientific marketing)
Innovative and results driven
A high degree of social confidence and interpersonal skills
Excellent time management skills; ability to set priorities
Ability to determine short and long range business needs
Must possess strong problem solving techniques
Must be willing to travel 25%-40%

Scientific Manager Resume Examples & Samples

PHD in relevant field, Degree must be from an accredited college/university according to the Council for Higher Education Accreditation (CHEA)
Minimum of 6 years of experience
Strong knowledge and experience in HPV immunology and vaccines
Experience in immune assay development and validation of ELISA and multiplex immune assays
Experience in plasmid and virus like particle production
PhD in immunology preferred
Experience in GCLP environment and understanding of regulatory requirements for vaccine development
Understanding of regulatory requirements and GCLP requirements
Experience with robotics and large scale testing of clinical trial samples

Scientific Manager Resume Examples & Samples

Conducts and collaborates with others on basic research and development relevant to long-term objectives and concerns
Writes and reviews manuscripts for publication
Develops strategies to ensure effective achievement of scientific objectives
Monitors and evaluates completion of tasks and projects
May develop budgets for capital expenditures and labor
Typically collaborates with other top managers to establish company policies
Makes final decisions on administrative or operational matte
Selects, develops and evaluates personnel to ensure the efficient operation of the function
Ph.D. from an accredited college/university according to the Council for Higher Education Accreditation (CHEA)
Must be able to obtain and maintain a Public Trust Clearance
A minimum of six (6) years of competent, innovative research experience
Strong knowledge of molecular biology and skills in the analysis of human specimens
Expertise in the field of oncology
Attention to detail and ability to identify and successfully address unexpected results
Ability to deliver high quality results in a timely manner
Proven ability to manage projects and staff as well as work independently
Ability to work within a highly matrix team environment
Ability to write and orally present data and project updates in a clear and effective manner
Must have first authorships on peer-reviewed publications, attendance and presentation experience at national meetings
Ability to preside over meetings showing leadership qualities, independence with sound ideas, vision and ability to remain focused on the mission/project
Experience with diagnostic assay development
Familiarity with human clinical studies where biomarker assays have been employed
Strong and proven technical skill and knowledge in genomics, molecular biological and genomic assay development
Experience in cancer genomics and/or signaling pathway analysis as well as assay development
Familiarity with clinical oncology studies or other protocol-driven clinical research

Senior Scientific Manager Resume Examples & Samples

BS + 12 years; MS + 8 years; Pharma D + 7 years; PhD + 6 years
Thorough knowledge of pharmaceutical development, including an understanding of current laboratory techniques, instrumentation, problem solving techniques, process engineering and manufacturing development, and statistics used in experimental work
Must have experience in global regulatory filings
Must demonstrate knowledge of several allied fields, such as chemical engineering, analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs. Fundamental understanding in DMPK, Pharmacology and Toxicology
Extensive knowledge of current Good Manufacturing Practices (cGMP), ICH Guidelines, other pertinent national regulations, and compendial requirements
Must have knowledge in global regulatory submission requirements and processes
Leadership– develops and uses knowledge and interpersonal skills to influence and guide stakeholders towards the accomplishment of program and divisional goals and objectives; adapts well to varied team dynamics and manages team members in a respectful manner
Risk Management – ability to identify/mitigate technical, budgetary, and schedule risks to multiple programs and propose appropriate risk response strategies
Communication – ability to expresses one’s self clearly and concisely to key stakeholders and functional management; documents issues and/or concerns concisely and comprehensively; adjusts style, language and/or terminology appropriate for the audience

Senior Manager European Scientific Publications Resume Examples & Samples

Leads product European Medical Team/s (EMTs) in establishing the publication strategy for the European region
Responsible for generating and executing the European publication plan according to timelines & deliverables agreed with the Global Publication Planning Team/s (GPPT/s)
Ensures that local and regional publication plans are part of the Global Publication Plan and are consistent with global strategy and messaging
Manages production, review & tracking of publications, ensuring the quality of publications from a content and editorial perspective
Establishes and manages outsourcing budget. Hires and manages vendors and contractors to write scientific publications (manuscripts, review articles, oral presentations, abstracts and posters)
Closely partners with multiple functions including medical communications, health economics, biostatistics, project management, medical directors, Amgen affiliates, and Global Medical Writing (GMW) & Publication Planning teams
Forms good working relationships with authors
Attends scientific congresses and advisory boards; writes reports if required
Produces updates as required for internal meetings (eg, with affiliates) on the status of publications for the product
Ensures compliance with Amgen publication policy and practices
Keeps abreast of professional information and technology

Scientific Services Manager Resume Examples & Samples

Ability to supervise and train others
Knowledge of GxP regulations and policies
Ability to follow oral and written directions
Problem solving ability and ability to meet needs of customers in a timely, efficient and cost effective manner
Oral and written proficiency in the prevailing language of the site of employment that permits clear oral and written communication in laboratory notebooks, forms and log books
Understands the current regulatory requirements for own discipline
Demonstrates understanding of impact on tasks being performed by Scientists and their work
Possesses customer service skills
BA/BS in a scientific discipline preferred
Three or more years of laboratory experience
At least one year experience in managing others in a lab environment. #LI

Global Scientific Manager Cardiology Resume Examples & Samples

You will define, control and conduct clinical studies with marketing relevance in the area of cardiology, working with the cardiology customers to define the outcome-related aspect of these studies
As part of your activities you will keep the global market for cardiology in your sights at all times and carry out regular analyses of this market, identifying risks and opportunities and suitable potential courses of action as well carrying out thorough strategic and business planning
You will work independently to draw up a successful, cross-portfolio marketing strategy for our product innovations relating to cardiology
You will function as a central interface between customers, sales, and marketing management at head office
Your duties will also include monitoring customer satisfaction on an ongoing basis and directly communicating requirements from customers and from sales to the development process
You will work in national and international teams and will be responsible for reviewing the optimum marketing strategy on an ongoing basis, as well as for planning and creating corresponding marketing material
You will also represent Siemens Healthineers at key international conferences of relevance to the sector
You have successfully completed university studies in medicine, preferably with a cardiological background
You have many years of professional experience and a sound knowledge of marketing
You demonstrate impressive clinical expertise and knowledge of processes in the healthcare system, and understand the cost drivers (for imaging in particular, but also in general)
Your strong presentation skills in English and your considerable persuasiveness will particularly distinguish you to an international audience of experts
You have a sound business knowledge of written and spoken English
As you will be spending at least one third of your working time on business trips to international conferences and customer cooperation visits, you must be very willing to travel
To complete your profile, you are results-oriented, have the ability to work in a team, and offer a pragmatic approach

Scientific Manager Resume Examples & Samples

BS + 9 years; MS + 5 years; Pharma D + 4 years; PhD + 3 years
Experience in one or more of the following disciplines: process chemistry, formulation development, analytical chemistry, biologics, and/or statistical analysis
Leadership – develops and uses knowledge and interpersonal skills to influence CMC teams towards the accomplishment of program goals and objectives; adapts well to different personalities and manages others on the team in a respectful manner
Risk Management – ability to identify technical, budgetary, and schedule risks to the program and plan appropriate risk response strategies
Communication – ability to expresses one’s self clearly and concisely to key stakeholders; documents issues and/or concerns concisely and comprehensively; adjusts style, language and/or terminology appropriate for the audience
Resource Management – ability to request internal and external resources (people, information, technologies, time, and capital) based on program needs

Senior Scientific Affairs Manager Resume Examples & Samples

Serve as a major point-of-contact in developing and maintaining relationships with key opinion leaders. Educate and provide supporting materials to speakers, authors, and opinion leaders. Maintain membership in key professional associations. Develop and maintain knowledge of trends in the industry including research developments, and new concepts in medical treatment and scientific technology, giving perspective to field activities associated with growing existing products, and bringing new products to market
Act as high level resource for customers, sales and marketing. Address customer’s scientific inquiries (on-label and off-label unsolicited requests), documents requests and actions, supports customer scientific and clinical applications
Liaise with Global Medical and Scientific Affairs, product development, marketing, sales and operations teams to scientifically support commercialization of Roche products (e.g. scientific and clinical content development, etc.). Acts as single point of contact between Roche and advisers
Develop strategies and priorities for clinical studies that support existing products and new products in development
Support molecular materials for content review and management in VEEVA
Coordinate continuing education workshops, seminars, and training programs for graduate physicians, pharmacists, scientists and health and medical personnel. Conceptualize, organize and analyze data, interpret, and synthesize complex clinical and non-clinical statistical reports to derive key outcomes and messages. Translate scientific and technical issues for diverse audiences

National Scientific Affairs Manager Resume Examples & Samples

Lead your field-based team to implement market advances through the creation and communication of scientific information, education, clinical practice change,
Lead the development and engagement of key opinion leader relationships in order to drive product value proposition
Develop strategies and priorities for the team that support existing products and new products in development
Educate and provide supporting materials to speakers, authors, and opinion leaders. Maintain membership in key professional associations. Develop and maintain knowledge of trends in the industry including research developments, and new concepts in medical treatment and scientific technology, giving perspective to field activities associated with growing existing products, and bringing new products to market
Act as high level resource for customers, sales and marketing. Addresses customer’s scientific inquiries (on-label and off-label, unsolicited requests), documents requests and actions, supports customer scientific and clinical applications

Scientific Manager Resume Examples & Samples

Leading and developing staff in the in vitro ADME team
Expanding the in vitro business and developing and implementing a strategy to enhance the in vitro ADME portfolio
Meeting with current and potential new clients, both on and off-site, so business travel will be a requirement of the role
Assisting the Head of Department in setting business goal and assessing performance against these goals

Senior Scientific Affairs Manager Resume Examples & Samples

Collaborate with global medical affairs and business colleagues to develop medical plans, identify gaps in current knowledge, and oversee study management of Investigator-Initiated and Roche-Sponsored Studies within the sequencing business area. Conduct briefings and collaborations with Roche technical and global partners
Be responsible for medical plan & study budget. Coordinate activities between cross-functional teams of internal and external partners across different sites. Manage resource and budget allocation according to project demands and requirements
Provide critical review of scientific information and data, generating timely feedback and insight to Roche partners
Be the key representative in identifying external partners and assisting in negotiating terms for collaborative projects or service contracts
Influence key decision-makers within the organization through fair and balanced scientific and medical evidence
Identify novel trends, new emerging technologies and potential partnering opportunities

Scientific Affairs Manager Resume Examples & Samples

Responsible for implementing and maintaining the effectiveness of the quality system
Provides scientific input for promotional and commercial activities as requested
Organizes and leads scientific meetings
Develops and maintains a network of key opinion leaders
Serve as scientific representative during Regulatory bodies interactions as needed
Provides scientific support for direct customer interactions as needed
Assists the team in strategic planning for scientific activities to ensure that business needs are met
Reviews scientific information and ensures effective internal communication of new scientific knowledge

Scientific Affairs Manager Resume Examples & Samples

Provide information on research developments, and new concepts in medical treatment, giving perspective to field activities associated with growing existing products, and bringing new products to market
Stay current on research developments and new concepts in medical treatment, giving perspective to field activities associated current or new products
Deliver critical scientific exchange including medical/scientific education and replies to unsolicited “off-label” inquiries in support of healthcare professionals, Roche scientific support groups and local and global business teams
Support the efficient planning, tracking and timely communication of key data

Scientific Affairs Manager Resume Examples & Samples

Act as high level scientific, medical and educational support for customers, sales and marketing. Address customer’s scientific inquiries (on-label and off-label unsolicited requests), documents requests and actions, supports customer scientific and clinical applications consistent with Roche’s Good Promotional Practices (GPPs)
Provide internal communication of customer projects. Conduct literature reviews, authors, edits, formats and consolidates information related to existing products and product development. Communicate investigator initiated study progress / findings to internal/external stakeholders
Build relationships with thought leaders
Educate and demonstrate the benefits of key products to scientific and clinical customers
Coordinate continuing education workshops, seminars, and training programs for graduate physicians, scientists and health and medical personnel. Conceptualize, organize and analyze data, interprets, and synthesize complex clinical and non-clinical statistical reports to derive key outcomes and messages. Translate scientific and technical issues for diverse audiences
Attend appropriate U.S. and international scientific congresses. Develop in-depth understanding of clinical practices and regulations, maintain understanding and insight into current lab and clinical practices and guidelines and investigate and report internally on competitor technologies and products

Scientific Manager, Immunology Resume Examples & Samples

Contributes to the overall management of the Immunotherapy Platform across MD Anderson Departments and multi-institutional consortium networks. Establishes, develops, and fosters collaborative relationships with industry and academic leaders to assure advancement of organizational and platform goals. Ensures systems, policies and procedures are in place to facilitate successful collaborations
Ensures that strategic and tactical plans for the ongoing activities of the platform are developed and executed efficiently. Provides scientific input for all aspects of the platform including protocol management, budgets, contracts, and specimen procurement
Reviews, evaluates, interprets, and integrates medical records, patient data, patient specimens, and/or test results and provides correlation with the different laboratory analyses, including but not limited to flow cytometry, molecular pathology, Nanostring technology, murine/pre-clinical studies, etc
Exhibits understanding of the processes of clinical research and pharmaceutical product development/approval
Attends and may lead the face-to-face and/or teleconference IMT meetings with alliance partners and academic collaborators: able to give data presentations and facilitate discussions regarding the advancement of science and research
Assigns/manages tasks to ensure platform deadlines and milestones are met. Develops reports, Gantt charts, and other tracking tools to ensure ongoing updates are available to Immunotherapy Platform staff
Works closely with the department administrator, faculty, research management team, and informatics staff to address issues and coordinate the development and implementation of operational solutions related to research protocols and electronic research applications
Writes and prepares various reports. May assist in the writing and planning of research grants

Senior Scientific Affairs Manager Resume Examples & Samples

Relationship Building. Serve as a major point-of-contact in developing and maintaining relationships with key opinion leaders. Educate and provide supporting materials to speakers, authors, and opinion leaders. Identify and report on trends in the industry, including research developments, competitive products, and new concepts in medical treatment and scientific technology
Scientific Resource. Serve as high level resource for external and internal customers, including the Roche commercial team. Addresses customer’s scientific inquiries (on-label and off-label) and documents requests and actions. Supports customer scientific and clinical interactions. Translates scientific and technical issues for diverse audiences
Liaison. Provide US perspective for US and Global Medical/Scientific Affairs, product development, marketing, sales and operations activities to scientifically support commercialization of Roche products (e.g. scientific and clinical content development, etc…)
Investigational Studies. Serve as primary point of contact for investigator-initiated studies (IIS) and leads activities for submission, approval, ongoing, and closure activities. Prioritize IIS that support medical plans for existing products as well as new biomarker utilization. Oversees activities of cardiac project coordinator
Education. Serve as resource for Medical/Scientific Affairs and cardiac Medical Scientific Liaisons. Conceptualizes, organizes and analyzes data, interprets, and synthesizes complex clinical and non-clinical statistical reports to derive key outcomes and messages

Scientific Manager Resume Examples & Samples

2+ years of experience with post-graduate work, including using technical expertise to write and discuss scientific concepts
2+ years of experience with organizing and facilitating scientific meetings
Experience as a biomedical scientific researcher or biomedical scientific research manager
Active Secret clearance required
MS degree required
2+ years of experience as a science or health journalist or editor of a scientific journal
Experience in interacting effectively with or facilitating various types of people, including senior executives, government leaders, researchers, clinicians, and advocates
PhD degree preferred

Bioanalytical Scientific Manager Resume Examples & Samples

Experience in the pharma or CRO industry supporting regulatory bioanalysis of small or large molecules
Extensive knowledge of a range of bioanalytical techniques including LC-MS/MS, immunoassay, flow cytometry and quantitative PCR to support the analysis of pharmacokinetic and pharmacodynamics endpoints (e.g. NCEs, NBEs, ADA and biomarkers)
Extensive knowledge of the latest regulatory standards required for GXP studies, including international guidance’s published by regulatory agencies such as FDA, EMA
Experience working with a wide range of internal stakeholders, including non-clinical safety, DMPK, clinical pharmacologists, translational medicine, clinical operations and quality assurance colleagues
Previous experience managing CROs to ensure appropriate level scientific and technical content is provided in support of programs
Demonstrated ability to influence teams to ensure bioanalytical data generated is of the highest quality

Manager of Scientific Affairs Resume Examples & Samples

Advanced degree in nutrition or a related field with a minimum of ten years of responsible experience in the industry is required
Strong understanding of human nutritional products is required
Must be computer literate with advanced knowledge of Excel and PowerPoint
Project management skills highly desired
Must have strong presentation skills; experience in presenting at trade shows, conferences and webinars is highly desired
Must be able to work effectively both as part of a team and as an individual
Must be eligible to work in the US

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