Samahitha is inviting applications for the position of Clinical Research Coordinator (CRC) in Bengaluru, Karnataka. This opportunity is ideal for freshers or candidates with up to 6 months of clinical research experience who are looking to start or accelerate their career in the clinical trials domain. Immediate joiners are strongly preferred.
This Clinical Research Coordinator job in Bengaluru offers hands-on exposure to clinical trial operations, regulatory submissions, trial master file (TMF) management, site coordination, and sponsor communication, making it a strong foundation role in the clinical research industry.
Job Details
- Designation: Clinical Research Coordinator
- Experience: 0 to 6 Months (Freshers eligible)
- Location: Bengaluru, Karnataka
- Employment Type: Full-time
- Industry: Clinical Research / CRO
- Joining: Immediate
Key Responsibilities
As a Clinical Research Coordinator, the selected candidate will be responsible for:
- Maintaining strict confidentiality of proprietary and sponsor-related clinical trial information
- Coordinating and overseeing subcontractors such as clinical laboratories, translation agencies, and document printing vendors
- Developing and customizing study documents including Study Management Plans, Monitoring Plans, Informed Consent Forms, IMP labels, and trial-specific forms
- Managing translations and regulatory submissions for assigned clinical trials
- Preparing, verifying, and maintaining regulatory submission packages and approval documentation
- Supporting investigator meetings and representing Samahitha during study-related discussions
- Handling adverse event (AE) reporting during the course of the clinical trial
- Managing clinical trial supplies, drug accountability, storage requirements, and site-level documentation
- Developing and maintaining the Trial Master File (TMF) and ensuring inspection readiness
- Planning and coordinating site initiation visits (SIV), routine monitoring visits, and site close-out visits
- Coordinating with CRAs and CTAs, reviewing monitoring reports, and supporting study administration databases
- Managing data clarification processes and supporting co-monitoring visits when required
- Providing regular study updates, newsletters, and communication to investigators and internal teams
Qualifications & Skills Required
- Degree in Pharmacy, Life Sciences, Clinical Research, or related discipline
- 0–6 months of experience in clinical research or clinical trial coordination
- Basic understanding of ICH-GCP guidelines and clinical trial processes
- Knowledge of regulatory documentation and TMF management
- Strong communication, documentation, and coordination skills
- Ability to work with cross-functional teams and multiple stakeholders
- Willingness to join immediately
Salary & Benefits
- Salary Range: ₹2.5 – ₹4.0 LPA (based on experience and interview performance)
- Exposure to end-to-end clinical trial operations
- Strong learning and career growth opportunities in a CRO environment
- Opportunity to work with sponsors, investigators, and global clinical research teams
How to Apply
Eligible and interested candidates can apply by sending their updated resume to:
Tip: Mention “Clinical Research Coordinator – Bengaluru” in the subject line for faster shortlisting