Research Assoc Job Description
Research Assoc Duties & Responsibilities
To write an effective research assoc job description, begin by listing detailed duties, responsibilities and expectations. We have included research assoc job description templates that you can modify and use.
Sample responsibilities for this position include:
Research Assoc Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Research Assoc
List any licenses or certifications required by the position: ACRP, ALS, NEALS, CRA, HIPPA, PEERRS, SOCRA
Education for Research Assoc
Typically a job would require a certain level of education.
Employers hiring for the research assoc job most commonly would prefer for their future employee to have a relevant degree such as Bachelor's and Doctoral Degree in Education, Communication, Science, Biology, Public Health, Psychology, Health, Biochemistry, Social Science, Molecular Biology
Skills for Research Assoc
Desired skills for research assoc include:
Desired experience for research assoc includes:
Research Assoc Examples
Research Assoc Job Description
- Ensure continued acceptability of the investigator, clinical site team and facility
- Review clinical data, source documentation, CRF, and investigative site regulatory files
- Work closely with data management and site to resolve discrepancies
- Ensure investigational product accountability accuracy and oversee investigational product inventory
- Liaise with vendors such as central laboratories as required to ensure protocol adherence and ensure investigational sites have appropriate clinical supplies
- Meet with clinical study sponsor representatives, as requested
- Submission of routine monitoring visit reports and follow-up letters as per required timelines
- Ensure resolution of issues with investigative sites
- Attend meetings as assigned and report on actions
- Function as a mentor for team members
- Maintain awareness of current developments in therapeutic area relative to assigned projects
- Throughout the conduct of the clinical trial assesses adherence to SCRI SOPS, GCP and all applicable regulatory requirements
- Three years direct oncology monitoring experience in Phases l - lll
- Prepares design validation plans that meet product design goals
- Monitors clinical studies
- Reviews data
Research Assoc Job Description
- Maintains professional
- Assumes responsibility for attending training sessions
- Lead research and recommendations for hedge fund investment opportunities
- Identify and lead creative industry research projects and white papers
- Exhibit strong knowledge of finance and investment theory and practice and the ability to apply this knowledge to client and practice/research area work
- Manage and deliver loosely defined and complex practice/research area work and client projects without supervision
- Make presentations to and deal directly with clients on most, if not all, firm advice
- Drive internal and external business development initiatives
- Contribute as a specialist consultant to the completion of RFP’s and presentations for business development opportunities with prospective clients
- Provide leadership that contributes to the success of a practice/research area
- Recruit participants for interviews and focus groups in person, by telephone and through email
- Co-authorship of peer-reviewed papers
- Seven to ten years hedge fund investing, principal investing, investment consulting, or related experience
- A strong understanding of investment concepts, specifically hedge funds and the financial markets
- Deep knowledge and contacts within the hedge fund industry
- Team player who can work with a team located in three offices (London, Chicago, New York)
Research Assoc Job Description
- Support screening and recruitment activities toward goal of enrolling 160 eligible participants into treatment phase of study by early 2017
- Review medical records to identify inclusion and exclusion criteria of candidates
- Maintain record of recruitment activities including source of referral, contacts with candidates, disposition of candidates
- Work with the study nurse coordinator and recruitment coordinator to schedule participant visits according to study requirements
- Facilitate subject preparation for study visits (e.g., review visit preparation with subjects, visit reminder calls, appointment letters)
- As directed by study clinical staff, contact study participants between visits to obtain clinical information including tolerance of medication, reports of hypoglycemia, and blood glucose records
- Ensure appropriate resources (space, research staff) are available for study visits
- Prepare materials for subject visits, including laboratory collection kits, source documents and case report forms (CRF) and any required equipment and study medications
- Monitor and maintain inventory of study materials and supplies
- Direct interaction with clinical subjects may include obtaining biological samples, physical examinations (e.g., blood pressures, waist and hip measurements) and administration of questionnaires
- Process, package, and ship biological samples to central laboratory according to study protocol
- Maintain study source documentation and database of UM GRADE study participants
- Assist the study coordinator and investigators in preparation of regulatory submissions, including reporting of amendments, adverse events, administrative updates to UM IRBMED, and reporting same to GRADE data coordinating center and other regulatory bodies as required
- Post-secondary education of Associates degree or higher in life/health sciences or professional certification from an accredited program or experience in clinical research or health care
- Proficiency using MIChart (UMHS Electronic Medical Record System)
- Current PEERRS and HIPPA certification
Research Assoc Job Description
- Computer proficiency (Microsoft Word, Access, Excel, Power Point)
- Ability to work and communicate with a multidisciplinary team of physicians, scientists, nurses and medical assistants in an outpatient clinical setting
- Prior direct patient contact experience in an inpatient or outpatient health care setting
- Prior experience working and interacting with patients in a clinical research setting and/or prior research study recruitment experience
- Trained in phlebotomy/venipuncture
- Laboratory experience including centrifuge use, sample preparation, packaging and shipping
- Experience in entering electronic case report forms using MIDAS or other data entry platform
- Coordinates the activities of enrolling center staff at member institutions and core laboratories as they relate to clinical/study responsibilities including training, data collection, operations, and communication with travel to institutions as necessary
- Ensures compliance with applicable regulatory requirements and IRB standards
- Develops and writes operational procedures for data quality control and data form construction with specific attention to clinical variables and continuity including internal study-specific work instructions
- Knowledge of cGMP manufacturing and familiarity with engineering concepts
- Ability to establish and maintain accurate documentation under appropriate guidelines
- Assists with development of recruitment strategies, information and database systems, training invoicing, forms, reporting and study tracking (timeline systems) per contractual requirements
- Booking transportation
- Maintaining and genotyping mouse colonies
- Minimum one (1) year of experience in of the technical areas required - Professional certification (e.g., RN, RHIT, RD, ) may substitute for two (2) years of experience
Research Assoc Job Description
- Research customer account information
- Sorts, batches and scans correspondence and routes according to procedures
- Returned Statements - Reviews, prioritizes and processes returned statements for address correction utilizing various systemic platforms
- Returned Credit Cards - Reviews, prioritizes and processes returned credit cards for address correction utilizing various systemic platforms
- Completes processing of customer send back items
- Prepares all outgoing mail and packages daily, to include USPS, FED EX, DHL, Completes all tracking reports as needed
- Processes returned checks and applies appropriates fees
- Supports Mail Clerk duties as needed, dependent on volume and coverage
- Fulfills check copy and audit requests as needed
- Meet established deadlines and productivity standards
- Basic knowledge of questionnaire design&simple data analysis & interpretation
- Knowledge of computer applications, such as word processing, spreadsheet design, & database applications
- Experience using research databases and reference management software such as PubMed, Medline, Google Scholar, Endnote, RefWorks
- Some supervisory experience or experience providing work direction is preferred
- Proactive, goal-oriented individual with ability to plan, direct, implement and monitor programs and projects effectively
- Strategic planning skills with ability to develop fundraising strategies