Job Description
Join MedTech Innovations at the forefront of medical breakthroughs as a Clinical Research Coordinator. We're seeking a passionate professional to manage complex clinical trials in our cutting-edge Boston facility. You'll collaborate with multidisciplinary teams to ensure regulatory compliance, patient safety, and data integrity while advancing revolutionary treatments. This role offers competitive compensation, comprehensive benefits, and the opportunity to transform healthcare outcomes.
Responsibilities
- Oversee end-to-end clinical trial execution including protocol development, site monitoring, and regulatory submissions
- Coordinate investigator meetings and ensure adherence to GCP and FDA guidelines
- Manage patient recruitment strategies and maintain ethical trial conduct
- Analyze and interpret clinical data using advanced statistical methodologies
- Maintain electronic Case Report Forms (eCRFs) and ensure data accuracy
- Liaise with sponsors, CROs, and IRBs to resolve protocol deviations
- Prepare comprehensive trial reports for FDA submissions and internal stakeholders
Qualifications
- Bachelor's degree in Nursing, Pharmacy, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in FDA-regulated trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in ICH-GCP, FDA regulations, and clinical trial management systems
- Strong data management skills with experience in eCRF platforms
- Exceptional organizational abilities with meticulous attention to detail
- Proven success in patient recruitment and retention strategies
- Excellent written/verbal communication and cross-functional leadership