Clinical Researcher Job Description
Clinical Researcher Duties & Responsibilities
To write an effective clinical researcher job description, begin by listing detailed duties, responsibilities and expectations. We have included clinical researcher job description templates that you can modify and use.
Sample responsibilities for this position include:
Clinical Researcher Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Clinical Researcher
List any licenses or certifications required by the position: IATA, CPC
Education for Clinical Researcher
Typically a job would require a certain level of education.
Employers hiring for the clinical researcher job most commonly would prefer for their future employee to have a relevant degree such as University and Master's Degree in Teaching, Supervision, Communication, Science, Graduate, Speech, Allied Health Sciences, The College, Department of Communication Sciences and Disorders, Medical
Skills for Clinical Researcher
Desired skills for clinical researcher include:
Desired experience for clinical researcher includes:
Clinical Researcher Examples
Clinical Researcher Job Description
- Design, development, and implementation of innovative, pragmatic digital medicine research programs working with a wide range of funders, NIH, non-government organizations, and industry
- Collaborate extensively with internal and external partners to drive innovation
- Present and publish the results of research programs
- Plan and perform laboratory research experiments and maintain accurate documentation of experimental protocols and perform mathematical analysis of data
- Prepare figures and text for submission of manuscripts
- Supervise and train staff in laboratory research techniques and collection
- Translate business needs and literature data into a clinical study
- Assess scientific feasibility of the study protocol and be involved in the investigator selection process
- Write the scientific part of Statistical Analysis Plan
- Write the clinical report upon completion or termination of studies
- Experience with regulations and legislation regarding the protection of human subjects
- Familiarity with the Institutional Review Board
- PhD in Nursing, or other advanced degree in clinical healthcare
- A minimum of 5+ years of experience creatively and independently applying research and experimental methodologies to answer real-world, healthcare-related questions
- Track record of impactful scientific publications
- Experience with grant writing and submissions
Clinical Researcher Job Description
- Safeguard the quality of your studies
- Liaise with doctors, scientists and health professionals
- Build internal and external networks of Key Opinion Leaders/investigators/experts and other stakeholders
- Experience and/or the ability to be a member of the IRB Committee and/or a Expedited reviewer for biomedical and/or behavioral research
- Conduct health outcomes research and quality improvement efforts, including clinical decision support efforts, grant writing, prepare and present findings at local, regional, national and international scientific meetings, prepares manuscripts and publishes findings and research in peer-reviewed journals)
- Serves as project leader for COM-P/Banner collaboration in current and future clinical decision support efforts, including ARDS, heparin-induced thrombocytopenia, projects addressing detection and treatment of septic patients, and others
- Participates in all other division efforts, even when not project leader, including, but not limited to those pertaining to pharmacogenetics, acetaminophen research, long QT intervals and torsades de pointe, and others
- Teach clinical decision support sciences to medical students, residents and fellows
- Serves as faculty member of the post-doctoral fellowship training committee for the Division of Clinical Data Analytics and Decision Support
- Provides expertise in biomedical statistics, epidemiology and research design for the Division of Clinical Data Analytics and Decision Support
- Able to work independently in preparing experimental protocols, and adept in the analysis of the relevant scientific literature and in the interpretation of experimental results
- Demonstrated ability to take initiative and work as a team-player or independently
- Must be detail-oriented and have strong problem-solving and organizational skills
- Must be flexible and cooperative to field and appropriately prioritize requests from supervisor, faculty, fellows, and staff
- Flexible to work outside of standard business hours if/when dictated by the time of tissue procurement
- Familiarity with preparing results for publication
Clinical Researcher Job Description
- Recognize the operational and technical needs of stakeholders and provide consistent and high quality results
- Collect and analyze process and operational data, facilitate groups involved in process design activities, and provide support for ongoing transition management and clinical process optimization
- Present analytical techniques, key findings, solutions, and deliverables to the Value Institute and hospital leadership
- Contribute to the advancement and dissemination of research and project work both scientifically and operationally
- Support the development, implementation, ongoing management, tracking and reporting of a variety of project activities
- Produce reports, presentations, publications, and/or white papers pertaining to ongoing and completed projects
- Assume a lead role on various projects
- Perform other related duties as required, including Value Institute’s internal administrative tasks
- Support and/or lead development of grant proposals as a team member or Principal Investigator
- Support institutional strategic plan by ensuring duties are aligned with institutional goals
- Two + years of relevant laboratory work experience
- Builds strong relationships with peers and cross functionally with partners outside of teams to enable higher performance
- Have relevant professional (inter) national collaborations universities, consortia, alliances
- Curiosity to connect science and methodologies into opportunities within one study and/or across different studies
- Ability to innovate and solve challenges with unique approaches
- Desire to mentor others to strengthen their skill and abilities
Clinical Researcher Job Description
- Site management, including site qualification, initiation and monitoring
- Contribute to key research strategies and development
- Review and provide input to improve clinical operations efficiency
- Serve as Study Director/Principal Investigator for preclinical studies at an internal research facility
- Develop preclinical project strategy including studies, objectives, and timelines that support long-term project team goals and objectives
- Provide scientific input, research, and select appropriate preclinical models (in vitro, in vivo or ex-vivo) to achieve project team goals
- Lead preclinical study conduct including protocol development, study management, data analysis, interpretation, and reporting
- Assist in the development of models as needed to meet project or corporate objectives by working closely with internal and external staff and resources
- Influence decisions made by preclinical, R&D, other functional management, and project leadership within the scope of the function
- Influence and contribute to collaboration across all functions within the preclinical department, and across internal customer functions (such as R&D, Marketing, and Regulatory)
- Minimum of three years clinical practice experience required
- PhD in nursing or healthcare related field required
- Knowledge/application of health services and systems frameworks required
- Strategic thinking, time management, conflict resolution and decision making skills required
- Demonstrated resource management and stewardship required
- Expertise in conducting research and research utilization required
Clinical Researcher Job Description
- Lead technical assistance activities, including the provision of written and other guidance, to health care providers in support of quality reporting and payment policy
- Contribute substantively to developing and presenting training materials and clinical scenarios related to quality measures and patient assessment data
- Provide subject matter expertise in the development of clinical quality measures
- Prepare technical reports and contribute to client deliverables
- Participate in business development activities including identifying strategic opportunities and contributing to the preparation of proposals of significant technical complexity, contract value, or strategic importance
- Participate in preparing for and attending community events
- Conduct in person/phone screeners for study recruitment
- Manage follow-up study visits with participants
- Translate study-related materials from Spanish to English or vice versa
- Manage project questionnaires in Qualtrics and Microsoft Word
- Effective verbal and written communication skills to include grant writing, publications, and professional presentations required
- Ability to develop and oversee research/grant projects and budgets preferred
- Knowledgeable regarding health care trends and research priorities/directions at the national, regional and local level preferred
- Bachelor’s in Statistics, Public Health, Nursing or related relevant field
- Scientific expertise in the field of gut health (or related area) is an advantage and/or you are willing and able to become familiar in this field
- Passion to connect people and mobilize networks to work together to achieve high quality results