Full Time Non-exempt Position: 5719 Widewaters Pkwy
Hours: 8:00am to 4:00pm (with some flexibility)
Research Coordinator Job Duties:
- Oversees compliance to protocol; manages quality control, completion and submission of study documentation
- Data collection, analysis and monitoring
- Maintains subject and other study-related records, including regulatory files
- Ensures smooth, accurate progress of clinical trials and/or research studies
- Case management of protocol and enrollment of subjects, including patient follow up schedules
- Maintains regulatory documents
- Corresponds with IRB including writing applications, continuing reviews and adverse event reporting within regulatory guidelines
- Submits documents to sponsors in clinical trials
- Maintains device inventory in clinical trials
- Coordinates billing services in clinical trials
- Supports joint registry database for measuring and monitoring clinical outcomes
- Supports investigator-initiated research studies from initial protocol development through statistical analysis and manuscript publication
- Creates protocols, informed consent documents, Case Reports Forms, worksheets, databases, reports, and other tools to meet clinical trial and research study needs
- Facilitates research processes to maintain compliance with SOPs, GCP guidelines, sponsor regulations, and current regulations
- Performs literature reviews
- Provides training on research processes to staff members
- Develops SOPs and training tools
- Occasional travel between locations
Other Duties and Responsibilities:
- Other responsibilities as assigned
- May be asked to perform higher level of duties on occasion
Required Skills:
- Strong verbal and written communication skills with ability to express thoughts clearly to others at all levels of the organization.
- Excellent organizational and analytical skills along with ability to work on multiple tasks and meet deadlines in stressful situations.
- Detail-oriented with ability to maintain accuracy in data management, and understand and follow complex, detailed instructions
- Demonstrate self-sufficiency and resourcefulness in problem solving with the ability to function independently.
- Skilled in the use of computerized systems and databases
- Knowledge of Good Clinical Practices, FDA, HIPAA, and IRB regulations; an understanding of research procedures is preferred.
CITI Course certification is required. ACRP/SOCRA/other nationally recognized research certification is preferred.
Education:
- Bachelors degree in healthcare, research, or related field. Three years experience, preferably in a research environment, equivalent combination of education and experience will be considered.
- Exceptional organizational skills, attention to detail, interpersonal skills, and effective communication skills also required.
Experience:
- Three years experience, preferably in a research environment, equivalent combination of education and experience will be considered
Apply for Research Coordinator PositionBenefits of Working at SOS
- Work life balance, including weekends, evenings, and holidays off
- Part of a team that helps restore function in our community
- RNs, LPNs, and MAs work together in a team atmosphere
- Opportunities for overtime working SOS PLUS Walk-In Care
- On site and free parking, steps away from the office you work
- Educational assistance with reimbursements for expenses associated with continuing education courses
Pay Range: $24.55 - $37.25