Clinical Research Coordinator I, Preventive Medicine
About The Position
Following established policies, procedures, and study protocols, the Clinical Research Coordinator I provides assistance with clinical research studies. The role supports patient recruitment, evaluation, and consent; collects and organizes patient data; schedules study visits; may perform clinical tests such as phlebotomy and EKGs; and maintains and updates study data. The position reviews proposals for compliance with sponsor and organizational guidelines, verifies sponsor requirements, prepares data for analysis and entry, documents patient visits and procedures, and assists with regulatory binders, quality assurance and quality control procedures, interviews, and regulatory submissions. The position is based at The Brigham and Women's Hospital, Inc., with a hybrid work arrangement. It is a regular, 40-hour-per-week role on the day shift. Patient care is not required. Candidates completing a bachelor's degree may have six months from hire to provide degree-equivalency verification, or up to one year if starting on a per diem basis.
Requirements
- Bachelor's degree in a related field of study is required; experience may be accepted in lieu of a degree.
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Nice To Haves
- Some relevant research project work; 0–1 year preferred.
Responsibilities
- Review proposals for compliance with sponsor and organizational guidelines and verify sponsor requirements are met.
- Recruit patients for clinical trials and conduct phone interviews.
- Verify the accuracy of study forms and update them according to protocol.
- Prepare data for analysis and data entry.
- Document patient visits and procedures.
- Assist with regulatory binders and quality assurance and quality control procedures.
- Assist with interviewing study subjects.
- Assist with study regulatory submissions.
- Support clinical research studies, including patient evaluation and consent, data collection and organization, study-visit scheduling, clinical tests such as phlebotomy and EKGs, and maintenance and updating of study data.
Benefits
- Competitive base pay.
- Comprehensive benefits.
- Career advancement opportunities.
- Differentials, premiums, and bonuses as applicable.
- Recognition programs designed to celebrate contributions and support professional growth.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
