Senior Clinical Job Description
Senior Clinical Duties & Responsibilities
To write an effective senior clinical job description, begin by listing detailed duties, responsibilities and expectations. We have included senior clinical job description templates that you can modify and use.
Sample responsibilities for this position include:
Senior Clinical Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Senior Clinical
List any licenses or certifications required by the position: ASCP, MLS, MT, CCRA, CCRP, CPR, PMP, HTL, HT, BS
Education for Senior Clinical
Typically a job would require a certain level of education.
Employers hiring for the senior clinical job most commonly would prefer for their future employee to have a relevant degree such as Bachelor's and Master's Degree in Education, Nursing, Healthcare, Medical, Health Care, Life Sciences, Science, Life Science, Business, Pharmacy
Skills for Senior Clinical
Desired skills for senior clinical include:
Desired experience for senior clinical includes:
Senior Clinical Examples
Senior Clinical Job Description
- Provides training and education sessions regarding GNE brand(s) and their approved indication(s)
- Partners with clinical specialists in other ways/means by attending periodic account meetings
- Supportcollaboration of multiple disciplines and working relationships with corporate departments, divisions, and facility
- Supportproject teams in integrating CPOE and Order Set activities into their project plans
- Assist with training, mentoring, and development of junior employees, co-monitoring
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits
- Report, write narratives and follow-up on serious adverse experiences
- Participate in the development of protocols and Case Report Forms as assigned
- Participate in writing clinical trial reports as assigned
- Act as contact for clinical trial supplies and other suppliers (vendors) as assigned
- Must have demonstrated ability to lead PK/PD, Biopharmaceutics, and Pharmacometric activities from planning, implementation through completion
- Knowledge of standard business procedures (regulatory guidance, global regulations, SOPs)
- Ability to effectively present information to and respond to questions from groups of managers, sites
- Bachelor degree & above, clinical medicine would be preferred
- Strong people communication skill
- Good project management skill ( good planning, implementation and follow up) is required
Senior Clinical Job Description
- Ensures clinically integrated, patient centric care coordination with a focus on appropriate first PAC setting, appropriate PAC LOS, transitions of care and readmission avoidance
- Supports the concept of being a data driven organization, relying heavily on analytics and outcome reports to drive the business
- Conducts weekly team call with all team members
- Interviews, hires, and is ultimately responsible for the competency and compliance of all clinical field staff
- Directly supervises the Clinical Team Manager (CTM)
- Works with CTM to maximize colleague performance using nH based reports, audits, record reviews and field based observations
- Participates in MMR, reviews results with CTM and creates action plans for identified issues
- Conducts semi -annual and annual colleague performance reviews
- Supports the CTM in rounds facilitation, field staff observations, colleague recognition and coaching when needed
- Works with Market Leadership and Human Capital to determine staffing requirements to support work volume
- Registered nurse or clinical experience strongly preferred
- Is an expert user of patient care related information systems (preferred Cerner Millennium)
- Requires strong analytical and statistical skills and interpretive abilities to make recommendations for improvements or changes
- Significant clinical research/CRA experience including remote and clinical monitoring and experience in all phases of study life cycle, including start up, interim and close out
- Understanding of scientific process medical and statistical concepts
- Ability to resolve project-related problems and prioritize workload for self and team
Senior Clinical Job Description
- Collaborates with Network Manager to develop business relationship with local providers
- Works directly with the GM to review market performance and develop/refine clinical strategy to maximize KPI achievement
- Evaluates performance to benchmarks, goals and outcomes for all programs high cost, volume and risk conditions
- May makes recommendations on reporting and analytic needs of the market
- In conjunction with the GM, attends and participates in the JOC meetings
- Functions as a liaison to the Local Physician Champion (LPC) to manage readmissions and other in market needs
- Develops relationships with client/partner peers at the hospital and plan level
- Monitors Compliance to Implementation Protocols and/or Contract SLA
- Works collaboratively with the Health Services and Utilization Management departments and programs to ensure positive outcomes
- Monitors feedback from member satisfaction surveys and provider feedback and identifies process improvement opportunities
- Ability to understand and work with financial information
- In lieu of the above requirements, candidates with four (4) years of site management and/or registry administration experience will be considered
- Able to develop knowledge of the disease under study
- Able to develop knowledge of protocol, regulatory guidelines and requirements, and company SOPs
- Establishes and maintains effective relationships with customers (internal and external) and gains their trust and respect
- This position requires a Bachelor's degree with 5 years successful experience as a systems user representative or analyst
Senior Clinical Job Description
- Lead life sciences customers in the rapid configuration and implementation of applications to support clinical trial and content management needs in the form of the Vault Clinical suite (Vault CTMS, Vault eTMF, Vault Study Startup, Vault Investigator Portal)
- Define strategies and implementation program(s) for deploying the Vault Clinical suite across an organization globally
- The ISCS will develop performance assessment tools such as workflow diagrams, site profile summaries, and cycle/response time charts
- The ISCS will be able to organize and manage full system clinical training classes on key Synapse components
- The ISCS will be able to understand, develop, train and explain in detail the Synapse product development road maps
- Confirms appropriate management of investigational product by performing drug reconciliation and accountability and other related -Review research specimen sample shipments to central lab
- On-going review of site regulatory file for completeness and accuracy
- Track and report progress of study, including activities
- Assist CRM with Vendor identification and selection and payments vis a vis contractual agreements
- Assist in the planning and coordinating investigation meetings
- Experience leading projects and directing the efforts of multiple people is preferred
- Experience should include 1 year working in a health care environment in a clinical role
- 5-7 years’ patient care delivery experience as a Board Certified / Board Prepared Oncologist
- Advanced degree or equivalent education/degree in life science/healthcare strongly recommended if no previous experience in clinical research
- Involvement in cross-functional, multicultural and international clinical trial teams
- 10+ years’ direct experience working with clinical software solutions in clinical operations, TMF operations, and/or trial management
Senior Clinical Job Description
- Assist in recruitment of subjects for minimal risk studies
- Order and maintain supplies required for study procedures
- Blood sample handling and storage
- Maintain a database that records details of clinical trial shipments, and in collaboration with the CRA ensure that there are adequate supplies of clinical trial material to meet project needs
- Maintain Trial Master File up-dated
- Support Clinical Team
- File and maintain the study administrative files locally and send original documents to central TMF
- Distribute documents to investigational sites, ECs, or vendors as per requirements and distribute of communications and study documents to study teams
- Ensure full integration of statistics and statistical thinking into our daily research, product and process development, technology transfer and production
- Develop robust products, processes and analytical methods for products in the pipeline in alignment with the Quality-by-Design principles
- Identify variants associated with human phenotypes and interrogate human causal biology
- PhD in field related to Pharmacokinetics
- Demonstrates technical expertise on PK/PD projects
- Knowledge of Clinical Trial processes across pharmaceuticals, device and/or biotech sectors, specifically as they relate to document and data collection
- Proven track record leading high-impact global system implementation programs for life sciences as a consultant, business or IT lead and/or business sponsor for clinical systems
- Proven ability to manage diverse stakeholders, and ensure delivery to a high degree of satisfaction