Clinical Research Coordinator II
4 weeks ago
Job Summary:
The Dana-Farber Cancer Institute is seeking a highly skilled Clinical Research Coordinator II to join their team. This individual will be responsible for assisting in clinical program and research operations, with a focus on genetics and genetic counseling.
Key Responsibilities:
- Primary data collection and management of patient clinical information
- Timely collection of protocol-related samples and shipment to outside entities
- Maintenance of regulatory binders and study compliance with state, federal, and IRB requirements
- IRB protocol submissions, including amendments, continuing reviews, and minimal risk protocols
- Patient screening for protocol eligibility, informed consent, and registration to clinical trials
Requirements:
- Bachelor's Degree and 1-3 years of equivalent experience
- Prior Clinical Research Coordinator experience preferred
- Experience working in a medical or scientific research setting or comparable technology-oriented business environment
Competencies:
- Understanding of CRF completion, including timely and accurate transcription of study data
- Setting up, coordinating, and managing clinical research studies
- ICH/GCP and Federal Regulatory requirements
- DF/HCC SOPs
- Roles and responsibilities of other key departments within clinical research
Knowledge, Skills, and Abilities:
- Excellent organization and communications skills
- Strong interpersonal skills and ability to effectively interact with all levels of staff and external contacts
- Detail-oriented and ability to follow-through
- Ability to effectively manage time and prioritize workload
About Dana-Farber Cancer Institute:
Dana-Farber Cancer Institute is a leader in life-changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds.
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