Clinical Research Coordinator
FLORIDA FERTILITY INSTITUTE PA, Clearwater, FL, United States
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.
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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.
#J-18808-Ljbffr