Med Express Clinical Research Solutions Private Limited is a leading organization specializing in clinical research services. We are committed to advancing medical science by conducting high-quality clinical trials that ensure patient safety and regulatory compliance. Our team works closely with pharmaceutical companies, healthcare providers, and regulatory bodies to deliver reliable and ethical research outcomes.
Job Description: Clinical Research Coordinator
As a Clinical Research Coordinator (CRC) at Med Express, you will play a crucial role in managing clinical trials and ensuring smooth execution of research protocols. Your responsibilities will include:
- Coordinating and overseeing clinical trial activities at the site level.
- Ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Recruiting and screening study participants.
- Collecting, documenting, and managing clinical data accurately.
- Liaising between investigators, sponsors, and regulatory authorities.
- Monitoring patient safety and reporting adverse events.
- Maintaining study documentation and preparing reports.
- Supporting audits and inspections.
Key Requirements
- Minimum 1 year of experience as a Clinical Research Coordinator or in a related clinical research role.
- Strong knowledge of clinical trial processes and GCP guidelines.
- Excellent communication and organizational skills.
- Ability to work independently and as part of a multidisciplinary team.
- Location: Chhatrapati Sambhajinagar (Aurangabad).
Why Join Med Express?
- Opportunity to work with a reputed clinical research organization.
- Gain hands-on experience in diverse clinical trials.
- Professional growth and career advancement.
- Collaborative and supportive work environment.
How to Apply
Interested candidates with the required experience can send their updated CV to medexpress.hr@gmail.com. Please mention “Clinical Research Coordinator – Aurangabad” in the subject line of your email.