Clinical Research Coordintor
About The Position
The Clinical Research Coordinator in the Reproductive Endocrine Unit (REU) at Massachusetts General Hospital will work on studies of fertility/infertility and reproductive endocrinology. This role involves assisting with clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. The position requires adherence to established policies, procedures, and study protocols. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification. The role is onsite at 40R Blossom Street and is a regular, full-time position with a 40-hour work week on a day shift.
Requirements
- Bachelor's Degree in a related field of study.
- Some relevant research project work (0-1 year preferred).
- 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.
- Must include a cover letter in the application.
Responsibilities
- Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
- Recruiting patients for clinical trials and conducting phone interviews.
- Verifies the accuracy of study forms and updates them per protocol.
- Prepares data for analysis and data entry.
- Documents patient visits and procedures.
- Assists with regulatory binders and QA/QC Procedures.
- Assists with interviewing study subjects.
- Assists with study regulator submissions.
- Screening and recruitment of individuals for study participation.
- Ensuring protocol requirements are met.
- Collecting data for input into the research databases.
- Performing phlebotomy and vital signs assessments.
- Handling biological samples.
- Maintaining and updating regulatory documentation for compliance.
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses
- Recognition programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
