Job Description
Join BioPharm Innovations as a Clinical Research Associate and drive the future of medical breakthroughs. We're seeking a detail-oriented professional to oversee clinical trials, ensuring compliance with FDA regulations and GCP standards. This role offers the opportunity to work on cutting-edge therapies that impact global healthcare. Enjoy competitive benefits, flexible work arrangements, and a collaborative environment where your expertise makes a real difference.
Responsibilities
- Monitor clinical trial sites for protocol adherence and regulatory compliance
- Conduct site visits, audits, and data verification activities
- Coordinate with investigators, sponsors, and regulatory authorities
- Manage clinical trial documentation and reporting
- Ensure accurate data collection and integrity per ICH-GCP guidelines
- Develop and maintain study budgets and timelines
- Mentor junior staff and contribute to process improvements
Qualifications
- Bachelor's degree in life sciences, pharmacy, or related field
- 3+ years of clinical research experience in pharmaceutical setting
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Strong knowledge of FDA regulations, GCP, and ICH guidelines
- Exceptional attention to detail and documentation skills
- Experience with EDC systems (e.g., Medidata Rave, Oracle)
- Excellent communication and problem-solving abilities