Job Description
Join MedTech Innovations, a leader in cutting-edge medical research, as we revolutionize patient care through groundbreaking clinical trials. We seek a Senior Clinical Research Coordinator to oversee complex studies in our Boston facility. You'll collaborate with top-tier physicians, pharmaceutical partners, and regulatory bodies to ensure protocol integrity while advancing medical science. This role offers unparalleled growth in a supportive, research-driven environment with comprehensive benefits and competitive compensation.
Responsibilities
- Design and implement clinical trial protocols in compliance with FDA/ICH-GCP guidelines
- Manage patient recruitment, enrollment, and retention strategies for diverse populations
- Oversee data collection, quality control, and regulatory submissions
- Coordinate multi-disciplinary research teams including physicians, statisticians, and biostatisticians
- Ensure ethical conduct through IRB protocol management and adverse event reporting
- Analyze clinical data and prepare comprehensive study reports for stakeholders
- Maintain electronic data capture systems and regulatory documentation
Qualifications
- Master's degree in Clinical Research, Nursing, Life Sciences, or related field
- 5+ years of clinical trial coordination experience with Phase II-III studies
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Proven expertise in FDA/ICH-GCP compliance and regulatory documentation
- Strong proficiency with electronic data capture systems (e.g., Medidata Rave)
- Exceptional interpersonal skills for patient communication and team leadership
- Experience with oncology or cardiovascular therapeutic trials preferred