Job Title: Certified Clinical Research Coordinator
Location: The IVF Center, Winter Park, FL
Position Type: Full-time
About The IVF Center: The IVF Center in Winter Park is a leading fertility clinic dedicated to providing exceptional care and treatment to individuals and couples seeking fertility solutions. We are committed to offering the most advanced, evidence-based services in a supportive and compassionate environment.
Mission + Vision Statement: To transform the field of reproductive health by prioritizing the patient experience through extraordinary and innovative clinical care and by our commitment to education and research.
Position Overview: We are seeking a Certified Clinical Research Coordinator to join our dynamic team. This role will focus on overseeing clinical trials and research studies in the fertility field, ensuring that all processes align with regulatory guidelines and industry best practices. The ideal candidate will be highly organized, detail-oriented, and experienced in clinical research.
Key Responsibilities:
- Coordinate and manage clinical research studies from start to finish, including patient recruitment, data collection, and regulatory compliance.
- Ensure the proper documentation of research activities, including case report forms, informed consent forms, and clinical trial protocols.
- Monitor and maintain study timelines to ensure deadlines are met.
- Collaborate with physicians, staff, and external research organizations to ensure high-quality research practices.
- Provide support and guidance to patients participating in research studies, answering questions and addressing concerns.
- Maintain confidentiality and ensure patient privacy in accordance with HIPAA regulations.
- Prepare and submit necessary reports to regulatory bodies and sponsors.
- Assist in the preparation and submission of amendments to clinical trials protocols to the IRB
- Other duties as assigned
Qualifications:
- Certified Clinical Research Coordinator (CCRC) preferred.
- Minimum of 2 years of clinical research experience, ideally in the reproductive or fertility field.
- Strong understanding of Good Clinical Practice (GCP) and FDA regulations.
- Excellent communication and organizational skills.
- Ability to work independently and as part of a team.
- Proficient in Microsoft Office and clinical research software.
Benefits:
- Competitive salary.
- Comprehensive benefits package, including health insurance and paid time off.
- Opportunity to work in a supportive and innovative environment.
- Continuous professional development and training.
Job Type: Full-time
Pay: From $25.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Work Location: In person
