Senior Clinical Research Associate (Senior CRA) – Clinical Research Jobs in Bangalore
Location: Bangalore
Job Type: Full-Time
Department: Clinical Research
Experience Required: Minimum 3 Years of Clinical Monitoring Experience
Eligibility: Freshers are NOT eligible for this role
Qualification: Life Sciences Degree or Higher
About the Role
We are actively hiring an experienced Senior Clinical Research Associate (Senior CRA) for a leading clinical research environment in Bangalore, India. This opportunity is ideal for professionals with strong expertise in clinical trial monitoring, site management, regulatory coordination, and GCP compliance.
The selected candidate will play a key role in managing clinical trial activities from study start-up to closeout while ensuring compliance with international clinical research standards and regulatory requirements.
Key Responsibilities
Work in compliance with ICH E6-GCP guidelines, SOPs, and applicable regulatory requirements
Perform clinical trial feasibility assessments and site evaluation activities
Support project start-up and clinical trial set-up processes
Conduct site selection, site initiation, monitoring, and site closeout visits
Coordinate investigator/site contract negotiation and execution
Develop and locally adapt study-specific documentation
Maintain and manage Trial Master File (TMF) documentation throughout the study lifecycle
Facilitate regulatory submissions and ethics committee documentation
Organize and participate in Investigator Meetings and study-related discussions
Maintain strong communication with investigators, site staff, sponsors, vendors, and cross-functional teams
Assist Project Managers and Project Team Leads with study updates and issue escalation
Resolve site-level operational challenges and ensure timely action plans
Support CRF retrieval, query management, and data clarification processes
Participate in client meetings, teleconferences, and departmental collaborations
Ensure smooth project closeout activities and final site documentation completion
Required Skills and Qualifications
Minimum 3 years of experience in Clinical Research monitoring activities
Strong understanding of ICH-GCP guidelines, clinical trial regulations, and SOP compliance
Experience in site management, monitoring visits, and investigator communication
Excellent organizational, documentation, and communication skills
Ability to manage multiple clinical trial activities within timelines
Life Sciences degree or higher qualification required
Who Should Apply?
This role is suitable for experienced Clinical Research professionals including:
Clinical Research Associates (CRA)
Senior CRA Professionals
Clinical Trial Monitoring Specialists
Site Management Professionals
Clinical Operations Executives
Freshers or candidates without monitoring experience are advised to apply for entry-level CRA or Clinical Trial Assistant roles instead.
Why Explore Senior CRA Careers in India?
Senior Clinical Research Associate jobs in India continue to see strong demand across CROs, pharmaceutical companies, and biotech organizations. Professionals with monitoring expertise, GCP knowledge, and site management experience can access significant career growth opportunities in global clinical trials and clinical operations.
Apply for More Global Clinical Research Jobs
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