Are you looking for a Clinical Trial Associate job in Surat with a reputed medical device organization? Concept Medical is hiring a full-time Clinical Trial Associate to support clinical research operations, documentation, and compliance activities. This opportunity is ideal for candidates with 2–3 years of clinical research experience and strong knowledge of medical device regulations.
If you have hands-on experience in clinical trial documentation, CRF management, site compliance tracking, and audit preparation, this role offers structured exposure to end-to-end clinical operations.
Concept Medical is a globally recognized medical device company specializing in innovative interventional technologies. The organization plays a significant role in advancing cardiovascular and endovascular treatment solutions.
Job Overview
- Position: Clinical Trial Associate
- Location: Surat, Gujarat
- Job Type: Full-time
- Work Mode: On-site
- Experience Required: 2–3 years in Clinical Research / Clinical Operations
- Industry: Medical Device / Clinical Research
Key Responsibilities
The Clinical Trial Associate will provide administrative and operational support across various stages of clinical research including:
Clinical Documentation & Compliance
- Assist Project Managers and CRAs in updating clinical trial management systems.
- Prepare, distribute, file, and archive essential clinical documents.
- Maintain Main Study Files, CRFs, and Trial Master Files (TMF).
- Conduct periodic study file reviews for completeness and regulatory compliance.
Clinical Data & CRF Management
- Track and manage Case Report Forms (CRFs) and query resolution.
- Process Data Collection Forms including login, tracking, and quality checks.
- Support clinical data flow and documentation accuracy.
Quality & Audit Support
- Assist in preparing Quality Management System (QMS) documentation.
- Support internal and external audits.
- Ensure compliance with medical device regulatory requirements.
Administrative & Operational Support
- Coordinate investigator payments.
- Support slide preparation and presentations for sponsors and business development.
- Assist in meeting departmental and project milestones.
Required Qualifications
- Degree or equivalent experience in a Clinical Background (Life Sciences, Pharmacy, Clinical Research, etc.)
- 2–3 years of professional experience in clinical research or medical device trials
- Strong understanding of medical device regulations
- Excellent written and verbal communication skills
- Familiarity with clinical systems and documentation standards
Preferred Skills
- Knowledge of ICH-GCP guidelines
- Experience in audit preparation
- Strong documentation and organizational skills
- Attention to detail and regulatory awareness
Why Apply for This Clinical Trial Associate Job?
- Opportunity to work in the medical device clinical research domain
- Exposure to full-spectrum clinical trial operations
- Experience with regulatory documentation and compliance systems
- Growth potential in Clinical Operations and Regulatory Affairs
How to Apply
