Job Description
Join our pioneering team at MedTech Innovations where cutting-edge medical research meets transformative patient care. We're seeking a Clinical Research Coordinator to drive impactful studies in oncology and immunotherapy. Collaborate with world-class physicians, pharmaceutical partners, and multidisciplinary teams to advance clinical trials that shape the future of medicine. Enjoy comprehensive benefits, flexible scheduling, and a culture that champions innovation and professional growth.
Responsibilities
- Oversee end-to-end clinical trial management including protocol development, site initiation, and regulatory compliance
- Coordinate patient recruitment, informed consent processes, and data collection according to ICH-GCP standards
- Liaise between sponsors, investigators, and IRB to ensure protocol adherence and timely reporting
- Manage trial budgets, vendor relationships, and investigational product accountability
- Analyze and interpret clinical data to prepare regulatory submissions and study reports
- Mentor junior staff and implement continuous quality improvement initiatives
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in oncology trials
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Proficiency in electronic data capture systems (e.g., Medidata Rave) and regulatory databases
- Demonstrated expertise in FDA regulations, ICH-GCP, and 21 CFR Part 11 compliance
- Exceptional organizational skills with ability to manage multiple complex protocols simultaneously
- Strong written/verbal communication skills for stakeholder engagement and documentation