Job Description
Join BioVita Innovations, a leader in cutting-edge pharmaceutical research, and shape the future of medicine as our Senior Clinical Research Associate. Based in Cambridge's biotech hub, you'll drive critical clinical trials for groundbreaking therapies while collaborating with world-renowned scientists and regulatory experts. We offer a dynamic environment where your expertise directly impacts patient outcomes and scientific advancement. What You'll Achieve: Lead end-to-end clinical trial management, ensure protocol compliance, and mentor junior associates. Why BioVita? Competitive compensation, comprehensive benefits, and opportunities to present at international conferences. Apply today to accelerate your career in pharmaceutical innovation.
Responsibilities
- Design and oversee clinical trial protocols ensuring FDA/ICH/GCP compliance
- Monitor site performance, conduct site initiation/monitoring/closing visits
- Manage clinical documentation and regulatory submissions
- Analyze trial data and prepare safety/efficacy reports for leadership
- Mentor junior CRAs and optimize clinical trial processes
- Collaborate with cross-functional teams (medical, regulatory, biostatistics)
- Represent company at investigator meetings and industry conferences
Qualifications
- Master's degree in Pharmacy, Life Sciences, or related field
- 5+ years clinical research experience in pharma/biotech
- Certified Clinical Research Associate (CCRA) or equivalent certification
- Proven expertise in oncology/neurology therapeutic areas
- Advanced proficiency in eCRF systems (e.g., Medidata Rave)
- Exceptional knowledge of global regulatory requirements
- Strong leadership skills with 2+ years mentoring experience
- Excellent written/verbal communication for stakeholder management