Education: High school
Experience: 8+ years
- Be part of a mission-driven organization dedicated to health equity and social justice.
- Work in a supportive, inclusive, and culturally competent environment.
- Access to continuous learning opportunities and professional development.
- Contribute to groundbreaking health initiatives and research.
- Employer-sponsored health, dental, and vision insurance with two PPO plans and an HMO plan.
- PTO Exchange allows employees to turn unused PTO into liquid assets
- Employer-paid basic life insurance valued at one times the annual salary
- Voluntary Life and AD&D, and Short-term and Long-term disability
- Flexible Spending Accounts for healthcare and dependent care
- Tuition Reimbursement and Student Loan Forgiveness Programs; NHSC & PSLF
- Employee Assistance Program with 5 employer-paid counseling sessions
- 50% off at Brown Elephant Resale Shops and discounts at local businesses
The Clinical Research Coordinator position is responsible for supporting clinical research staff and managing new and ongoing clinical research activities. The position includes assisting clinical investigators and research staff to drive projects forward by interacting closely with external clinical research organizations and sponsors.
Preparation of all study documentation such as protocols, amendments, case report forms, SAE reports, and study reports is an integral part of this job. The Clinical Research Coordinator will adhere to GCP, ICH, and FDA guidelines in the conduct of all study-related activities.
- Provide study coordination for assigned trials as directed by the Clinical Research Manager; including data coordination and quality control of research data.
- Provide back-up and support for all areas of clinical research
- Complete regulatory paperwork for IRB submissions, annual reviews and study close-out
- Ensure that all Serious Adverse Events (SAEs) are reported in a timely fashion to IRB and sponsor
- Create and update Regulatory Binder for each assigned study
- Interact/liaise with study sponsors and investigators in role of study representative
- Conduct eligibility screening interviews over the phone and/or in person
- Schedule study patient appointments and make reminder calls to patients; send reminder letters and emails as appropriate
- Conduct study patient visits per protocol, including screening and follow-up visits, data collection and entry, specimen collection, and other study activities
- Communicate clinical trial status to management and staff through meetings and tracking system; maintain related records
- Create and update paper and electronic study patient records
- Participate in other recruitment/retention activities as needed, including calling potential participants and occasional outreach
- Attend trainings, staff meetings, and in-services as required
- Assist lab personnel with specimen processing and shipping as needed
- May be asked to attend Investigator Meetings for new trials as assigned
- High School Diploma/Equivalent & 8 years+ clinical research experience
- Possess the ability to prioritize while multi-tasking in a team setting or alone
- Working knowledge industry regulations, standards and guidance
- Effectively communicate with physicians, nurses, pharmaceutical companies and other team members.
- Requires ability to use computers, telephones and other office equipment.
- May require occasional bending and lifting up to 25 pounds.
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This posting was published by Howard Brown Health on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.