About the role
In this role, you will coordinate all aspects of clinical trials from start to finish. You will be responsible for preparing study protocols, recruiting participants, and ensuring that data is collected accurately and ethically. This position is ideal for a detail-oriented individual with a passion for advancing medical research and improving patient outcomes. Join a dedicated team that supports professional growth and innovative research practices.
What you'll do
- Prepare study protocols and informed consent documents
- Recruit and communicate with trial participants
- Ensure compliance with all regulatory requirements
- Collect and maintain accurate data throughout the study
What you'll need
- Bachelor's degree in Life Sciences or related field
- 2-5 years of experience in clinical research
- Strong understanding of clinical trial regulations
Skills
Detail-oriented and organized
Strong communication skills
Ability to work in a team
Good to have
Experience with data management software
Knowledge of statistical analysis
Benefits
- Professional development opportunities
- Health and wellness programs
- Team-oriented work environment
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are the main responsibilities of this role?
You will manage clinical trials, recruit participants, and ensure compliance with regulations.
What qualifications are required?
A degree in Life Sciences or a related field and experience in clinical research are essential.
Is this role onsite?
Yes, this is a full-time onsite position in Jammu.
What is the salary range for this position?
The salary ranges from INR 40,000 to INR 70,000 per month.
How can I apply for this job?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
Listing last updated