Job Description
Join our pioneering team at MediCore Solutions, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to lead pivotal studies that advance medical science and improve patient outcomes. As a cornerstone of our research division, you'll collaborate with world-class physicians, biostatisticians, and regulatory experts in state-of-the-art facilities. Enjoy comprehensive benefits including tuition reimbursement, flexible scheduling, and opportunities for international research collaborations.
Responsibilities
- Design and execute multi-site clinical trials adhering to FDA and GCP standards
- Manage complex protocol development, IRB submissions, and regulatory documentation
- Oversee patient recruitment, retention, and informed consent processes
- Analyze and interpret clinical data using SAS and R statistical software
- Liaise with pharmaceutical sponsors, CROs, and ethics committees
- Mentor junior research staff and ensure compliance with 21 CFR Part 11
- Present findings at international conferences and peer-reviewed journals
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years of clinical trial coordination experience in oncology or cardiology
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in EDC systems (Medidata Rave) and electronic source data
- Proven track record in managing FDA audits and inspections
- Strong statistical literacy and data visualization skills
- Exceptional project management with PMP certification preferred