- Bachelor of Science and relevant experience in clinical research compliance or auditing.
- Excellent interpersonal, writing, and analytical skills.
- Detail-oriented with excellent organizational and multitasking skills.
- Ability to work independently and as part of a team.
- Experience in oncology, REDCAP databases, specimen collection, and EPIC EMRs is desirable.
- Support all aspects of human biospecimen collection for research from head and neck cancer patients.
- Create and continuously update a list of clinical trials relevant to head and neck malignancy.
- Serve other discrete projects and infrastructure needs at the interface of clinical practice with head and neck cancer research.
- Manage study activities including subject recruitment, data entry, subject visits and follow-up, and regulatory documentation.
- Interact directly with Principal Investigators, other lab members, research staff, and patients.
- Adhere to all University of Pennsylvania, GCP/ICH, and FDA guidelines.
- Screen, recruit, and consent potential study participants as specified per protocol.
- Collect blood and other specimens and coordinate specimen storage and processing with various labs.
- Complete CRFs and data entry to study databases, sample process and shipping, patient reimbursement, research billing review, etc.
- Coordinate the administration of the investigational product and study related medications.
- Maintain all study-related documents.
- Prepare and participate in the conduct of audits by the study sponsors, CROs, the FDA, and other entities as required.
Clinical Research Coordinator - Philadelphia, United States - Proclinical Staffing
Description
Clinical Research Coordinator - Philadelphia, PA - Permanent
Proclinical is seeking a dedicated and enthusiastic Clinical Research Coordinator who is passionate about clinical-translational research in the field of head and neck cancer. This is a permanent position located in Philadelphia, PA.
Primary Responsibilities:
This role is ideal for someone interested in a career in science or medicine. The role will focus on three main areas: human biospecimen collection for research, updating a list of clinical trials relevant to head and neck malignancy, and serving other projects and infrastructure needs at the interface of clinical practice with head and neck cancer research.
Skills & Requirements:
The Clinical Research Coordinator will:
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at (+1) or .
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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