Job Description
Join our pioneering medical research team at GlobalMed Solutions, where innovation meets life-changing therapies. We're seeking a meticulous Clinical Research Associate to drive clinical trials from protocol to approval. Work alongside industry experts in state-of-the-art facilities while contributing to groundbreaking treatments that impact millions worldwide.
Why GlobalMed? Our collaborative culture combines cutting-edge technology with compassionate patient care. Enjoy comprehensive benefits, professional development opportunities, and the satisfaction of advancing medical science.
Responsibilities
- Monitor clinical trial sites for protocol compliance and regulatory adherence
- Conduct site visits, source document verification, and data quality audits
- Manage investigator relationships and facilitate communication between sites and sponsors
- Prepare regulatory documentation and ensure timely submission to ethics committees
- Analyze clinical data and identify trends requiring site intervention
- Maintain electronic trial master files and audit trails
- Train site personnel on GCP standards and study procedures
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research experience with Phase II-III trials
- Certified Clinical Research Associate (CCRA) or equivalent certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave, Oracle)
- Deep knowledge of ICH-GCP and FDA/EMA regulations
- Exceptional attention to detail and documentation skills
- Strong interpersonal skills for cross-functional collaboration
- Ability to travel up to 40% domestically