What are the responsibilities and job description for the Research Study Coordinator position at Humanity Clinical Research?
Job Summary:
We are seeking a dedicated and proactive Clinical Research Study Coordinator to join our team and support the execution of clinical trials at our research site. This role is ideal for a Foreign Medical Doctor (MD) looking to transition into the U.S. clinical research field. The Study Coordinator will manage day-to-day trial activities, ensure participant safety, and maintain compliance with study protocols and regulatory guidelines. This is an exciting opportunity to contribute to meaningful research in a dynamic and supportive environment.
Job Description:
We are seeking a highly motivated and detail-oriented Clinical Research Study Coordinator to join our clinical research team. The Study Coordinator will be responsible for managing the day-to-day operations of clinical trials while ensuring compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines.
Foreign Medical Doctors (MDs) with interest in transitioning into clinical research are highly encouraged to apply.
Key Responsibilities:
- Coordinate all aspects of clinical trials conducted at the site.
- Screen, recruit, and enroll study participants according to protocol eligibility.
- Obtain and document informed consent.
- Conduct study visits and collect data in compliance with the protocol.
- Maintain accurate and organized regulatory and source documentation.
- Collaborate closely with the Principal Investigator (PI), sponsors, and study monitors.
- Process and ship laboratory samples as per sponsor requirements.
- Report adverse events and protocol deviations in a timely manner.
- Ensure overall protocol compliance and readiness for audits/monitoring visits.
Qualifications:
- Foreign Medical Doctor (MD) preferred.
- Prior experience as a Study Coordinator or in clinical research (preferred but not required).
- GCP Certification required (or must be obtained upon hire).
- Strong organizational and time-management skills.
- Proficient in Microsoft Office and electronic data capture systems (EDC).
- Excellent verbal and written communication skills.
- Ability to work independently and as part of a collaborative team.
- Bilingual (English/Spanish) is a plus.
Benefits:
- Competitive salary
- Flexible work schedule (as applicable)
- Ongoing training and career development
- Professional and supportive work environment
- Opportunities for growth within the clinical research field
Job Type: Part-time
Pay: $20.00 - $25.00 per hour
Work Location: In person
Salary : $20 - $25