Clinical Research Coordinator

Job Description

Job Description

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:

• Bachelors 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.