Clinical Research Coordinator
2 weeks ago
Position: Clinical Research Coordinator
Location: Bowling Green, KY
Employment Type: Full-Time
About Us:
We are a dynamic and growing clinical research organization based in Bowling Green, Kentucky, dedicated to advancing medical knowledge and serving patients through high-quality clinical trials. Our team is committed to maintaining the highest standards of clinical research, patient care, and ethical practices.
Position Overview:
We are seeking an experienced Clinical Research Coordinator to join our team. The ideal candidate will have a strong background in clinical research coordination and be skilled in supporting clinical studies, including patient interaction, sponsor communication, and collaboration with other staff members. This role requires a high level of attention to detail, strict adherence to study guidelines, and excellent communication skills.
Key Responsibilities:
- Coordinate and manage clinical research studies from start-up to closeout in compliance with protocol requirements, GCP, and regulatory guidelines.
- Serve as a point of contact for study participants, sponsors, and research staff, ensuring effective and professional communication.
- Screen, recruit, and enroll study participants, ensuring informed consent and eligibility criteria are met.
- Schedule and conduct study visits, including data collection, patient assessments, and sample processing.
- Maintain accurate and up-to-date records, including source documents, case report forms (CRFs), and study databases.
- Ensure proper documentation and reporting of adverse events, protocol deviations, and other relevant study information.
- Collaborate with principal investigators and other team members to ensure successful execution of clinical trials.
- Monitor study progress, perform quality checks, and ensure compliance with study protocols, regulatory requirements, and internal SOPs.
- Assist in the preparation of study-related documents, such as regulatory submissions, study manuals, and progress reports.
- Participate in sponsor and regulatory audits, inspections, and monitoring visits as required.
Qualifications:
- Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and clinical trial processes.
- Exceptional organizational skills with high attention to detail and accuracy.
- Excellent communication and interpersonal skills for effective interaction with patients, sponsors, and research staff.
- Ability to work independently as well as collaboratively in a team-oriented environment.
- Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS) is preferred by not required.
- Certification as a Clinical Research Coordinator (CCRC) or equivalent is preferred but not required.
What We Offer:
- Competitive salary based on experience and qualifications
- Comprehensive benefits package including health, dental, and vision insurance
- Paid time off (PTO) and holidays
- Opportunities for professional growth and development
- Supportive and collaborative work environment
How to Apply:
Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience and why they are a great fit for this role. Please send your application to jallred@equity-med.com with the subject line “Clinical Research Coordinator Application – [Your Name].”
We look forward to welcoming a dedicated and enthusiastic professional to our team
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