Clinical Research Coordinator III
2 weeks ago
Job Title: Clinical Research Coordinator
Company: Confidential
The role of the Clinical Research Coordinator involves a variety of tasks related to research project management. Responsibilities include the preparation and review of scientific proposals, regulatory documents, and sponsor contracts, as well as overseeing the conduct of research, clinical services, and staff management for successful project implementation and closure.
Job Duties:
Conduct of Research
- Supervise clinical staff such as phlebotomists and sleep technicians
- Ensure comfort in clinical settings involving procedures like blood draws and biopsies
- Communicate study requirements to all involved individuals
- Coordinate participant tests, procedures, and data collection as per protocol
- Maintain study timelines and inventory of supplies
- Ensure proper documentation maintenance and participant communication
- Assist in recruitment strategies and informed consent processes
- Assist with protocol modifications and day-to-day study activities
- Perform cognitive assessments with older adults (preferred)
- Handle ad hoc assignments as directed
Reporting
- Assist with scientific and compliance reporting requirements
- Facilitate study registration procedures
Supervisory
- Provide leadership in clinical research projects
- Supervise and support student research assistants and staff
- Mentor and guide staff in study implementation and outcome review
Project Closeout
- Ensure timely submission of closeout documents
- Coordinate with relevant entities for study closure
Preparation and/or Review of Scientific Proposal
- Assist in protocol reviews and feasibility assessments
- Identify necessary resources and maintain participant privacy
Regulatory and IRB
- Prepare IRB submissions and other regulatory documents
- Maintain study files and essential documents
- Perform quality assurance and audits as necessary
Other
- Support daily research study activities
- Engage in miscellaneous duties as assigned
- Attend all required meetings and training sessions
Qualifications:
Expected Salary: $,-$, commensurate with education and experience.
Minimum Requirements: Bachelor's degree in an appropriate field and three years of relevant experience.
Preferred Qualifications:
EXPERIENCE
- Experience in healthcare or academic research
- Preferably worked with older adults
KNOWLEDGE
- Understanding of research participant recruitment regulations
SKILLS
- Proficiency in clinical-trials management systems and survey tools
- Strong skills in Microsoft Office and data analysis software
- Excellent communication skills
ABILITIES
- Capacity to meet deadlines and manage multiple projects
- Ability to work independently and in a team environment
- Effective communication of technical information
- Demonstrated creativity, attention to detail, and professionalism
OTHER QUALIFICATIONS
- Preferred degrees: Nursing, gerontology, psychology, or similar
- Phlebotomy certification preferred
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