Company Description
Zenovel specializes in delivering high-impact solutions across Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Regulatory Affairs in the pharmaceutical industry. With over 20 years of global experience, we support end-to-end clinical development, manufacturing compliance, and regulatory processes to ensure alignment with international standards. Our services include clinical trial oversight, facility audits, risk-based monitoring, and automation of trial processes. At Zenovel, we aim to simplify regulatory complexities and help clients achieve compliance-driven growth and success globally. Our headquarters is in Ahmedabad, and we are dedicated to helping pharma and biotech companies scale safely and efficiently.
Role Description
This is a full-time, on-site role based in Ahmedabad for a Clinical Research Associate. The Clinical Research Associate will be responsible for monitoring clinical trials, ensuring compliance with protocols, and managing day-to-day clinical operations. The role requires engaging in research, maintaining study documentation, and working collaboratively with clinical research teams to ensure the success of clinical trials.
Qualifications
- Familiarity with protocols and guidelines relevant to clinical research and trials
- Experience with Clinical Research Associate responsibilities and clinical operations
- Understanding of clinical trial processes and research methodologies
- Strong organizational, analytical, and problem-solving skills
- Effective communication and teamwork abilities
- Bachelor's degree or higher in life sciences, pharmacy, or a related field
- Knowledge of GCP regulations and international guidelines
- Experience in Phase I–III trials and understanding of diverse therapeutic areas is an advantage
