Job Description
Join Boston Medical Innovations at the forefront of groundbreaking medical research! We're seeking a passionate Clinical Research Coordinator to drive our oncology clinical trials forward. In this pivotal role, you'll ensure protocol compliance, manage patient data integrity, and collaborate with multidisciplinary teams to accelerate life-changing therapies. Enjoy competitive benefits, professional development opportunities, and the chance to make a tangible impact in patient care.
Responsibilities
- Oversee clinical trial execution including patient recruitment, screening, and informed consent processes
- Maintain accurate electronic data capture (EDC) systems and regulatory documentation
- Coordinate with IRB, FDA, and sponsors to ensure protocol adherence and regulatory compliance
- Train and mentor clinical research associates on SOPs and GCP standards
- Analyze and report adverse events, protocol deviations, and trial metrics
- Liaise with healthcare providers and patients to ensure protocol understanding and retention
- Prepare regulatory submissions and maintain trial master files
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Coordinator (CCRC) or equivalent certification
- 3+ years of experience in clinical trials with oncology focus
- Expertise in FDA regulations, ICH-GCP, and clinical trial management systems
- Strong data management skills with proficiency in EDC platforms (e.g., Medidata Rave)
- Exceptional communication and stakeholder management abilities
- Proven ability to manage complex timelines and competing priorities