Clinexel Life Sciences, a trusted full-service CRO, is inviting applications for the position of Clinical Research Associate (CRA). This is a great opportunity for professionals with clinical trial monitoring experience who are looking to grow their careers in a dynamic and compliant research environment.
If you have a strong understanding of GCP/ICH guidelines and are passionate about clinical research, this role offers the perfect platform to enhance your expertise.
Job Overview
Position
Clinical Research Associate (CRA)
Location
Sanpada, Navi Mumbai, India
Experience
2 to 3 years of relevant clinical trial monitoring experience
Qualification
Graduate or Postgraduate degree in Life Sciences or Pharmacy
Roles and Responsibilities
As a Clinical Research Associate, you will be responsible for:
- Conducting monitoring visits in accordance with study protocols
- Ensuring compliance with GCP/ICH guidelines and regulatory requirements
- Reviewing site performance and study progress
- Preparing monthly and annual monitoring reports
- Verifying data accuracy and protocol adherence at site level
- Supporting Project Managers in overall trial management
- Identifying and resolving site-related issues during trials
Required Qualifications
To be eligible for this role, candidates must have:
- Bachelorโs or Masterโs degree in Life Sciences or Pharmacy
- Hands-on experience in clinical trial monitoring
- Strong knowledge of regulatory guidelines (GCP/ICH)
- Good communication and documentation skills
- Ability to manage multiple sites and timelines
Salary and Benefits
- Expected Salary Range: โน3.5 LPA โ โน6 LPA (based on experience)
- Opportunity to work with a reputed CRO
- Exposure to diverse clinical trials and regulatory processes
- Professional growth and skill development
- Collaborative and supportive work environment
How to Apply
Interested candidates can apply by sending their updated resume to:
Make sure to mention โCRA Applicationโ in the subject line for better visibility.