Clinical Research Coordinator A (Affective Disorders Program)
About The Position
This position will assist in the management and data collection of multiple clinical trials and responsibilities in specific research area. Coordinate the screening of patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations. Works closely with the Principal Investigator, manager, and study team to identify problems and develop solutions. Implement approved changes to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects.
Requirements
- Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
- Must have a personal vehicle for this purpose. Mileage will be reimbursed.
Responsibilities
- Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry
- Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines
- Assure compliance with the protocol and regulatory requirements includes: collecting, recording, and maintaining data and source documentations.
- Be primarily responsible for traveling to participants' homes in the evening to set up equipment for sleep studies, and return in the morning to pick up equipment. Must have a personal vehicle for this purpose. Mileage will be reimbursed.
- Database management and analysis
- Ordering and stocking supplies, maintaining equipment
- Educate patients and family members
- Promote good clinical practice in the conduct of clinical investigations, included possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection
- Other duties and responsibilities as assigned
Benefits
- excellent healthcare
- tuition benefits for employees and their families
- generous retirement benefits
- a wide variety of professional development opportunities
- supportive work and family benefits
- a wealth of health and wellness programs and resources
- comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- flexible spending accounts
- tuition assistance
- generous retirement plans
- long-term care insurance
- wellness and work-life resources
- professional and personal development resources
- access to a wide range of University resources as well as cultural and recreational activities
- discounts and special services
- flexible work options
- forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia
- adoption assistance
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
