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Clinical Research Coordinator
Benefits:
- Competitive salary
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
About the Role:
Women's Medical Research Group i s looking for a Clinical Research Coordinator, who will play a pivotal role in advancing reproductive health research in addition to other research studies. This exciting position offers the opportunity to work closely with patients and contribute to groundbreaking studies in a supportive and innovative environment.
Responsibilities:
- Coordinate and manage clinical research studies from initiation to completion.
- Recruit, screen, and enroll study participants while ensuring informed consent is obtained.
- Collect, record, and maintain accurate data in compliance with regulatory standards.
- Collaborate with physicians and research staff to implement study protocols effectively.
- Monitor patient progress and manage adverse events throughout the study.
- Prepare and submit regulatory documents to Institutional Review Boards (IRBs).
- Assist in the training and mentoring of new research staff and interns.
- Stay updated on industry trends and best practices in clinical research.
Requirements:
- Bachelor’s degree in a related field; clinical research certification is a plus.
- 2+ years of experience in clinical research coordination or a similar role.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent communication skills, both verbal and written.
- Proficient in data management and electronic data capture systems.
- Ability to work independently and as part of a collaborative team.
- Detail-oriented with strong organizational and time management skills.
- Compassionate and patient-focused demeanor with a passion for reproductive health.
Submit your resume for review.
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