Methics Clinical Solutions Pvt. Ltd. is inviting applications for the position of Clinical Trial Associate (CTA). This opportunity is ideal for fresh graduates in Life Sciences who want to start a career in clinical research and clinical trial management.
Clinical Trial Associates play a critical role in supporting clinical research teams, maintaining regulatory documentation, coordinating trial activities, and ensuring compliance with Good Clinical Practice (GCP) guidelines.
Candidates passionate about clinical trials, regulatory compliance, and healthcare innovation are encouraged to apply.
Job Overview
- Position: Clinical Trial Associate
- Company: Methics Clinical Solutions Pvt. Ltd.
- Industry: Clinical Research / CRO
- Employment Type: Full-Time
- Experience: Freshers can apply
- Salary: As per industry standards
- Joining: Immediate Joiners Preferred
This role provides hands-on exposure to clinical trial operations, Trial Master File (TMF) management, regulatory documentation, and clinical study coordination.
Key Responsibilities
Selected candidates will support clinical research activities and assist the study team with operational and documentation tasks.
Major responsibilities include:
- Supporting clinical trial operations and study management teams
- Maintaining Trial Master File (TMF) and other essential regulatory documents
- Assisting with clinical site communication and coordination
- Tracking study progress and maintaining trial documentation
- Coordinating meetings, logistics, and internal study communications
- Ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines
- Supporting documentation required for clinical trial audits and inspections
This role helps candidates build strong expertise in clinical trial documentation management and clinical research coordination.
Eligibility Criteria
Candidates must meet the following qualifications:
Educational Qualification
- Bachelorโs degree in Life Sciences, Pharmacy, Biotechnology, or related discipline
Skills Required
- Strong attention to detail
- Good documentation and organizational skills
- Ability to manage multiple tasks in a fast-paced research environment
- Understanding of clinical research processes and regulatory compliance
- Strong communication and teamwork abilities
Fresh graduates interested in clinical trial operations, CRO jobs, and clinical research careers are encouraged to apply.
Why Join Methics Clinical Solutions?
Working at Methics Clinical Solutions offers exposure to the fast-growing clinical research and CRO industry.
Key benefits include:
- Hands-on experience in clinical trial operations
- Exposure to Trial Master File (TMF) management
- Opportunity to work with experienced clinical research professionals
- Experience in GCP compliance and regulatory documentation
- Career growth opportunities in clinical research, CRA roles, and clinical project management
This opportunity is especially valuable for candidates looking to start a career in clinical trials, CRO operations, or regulatory clinical research roles.
How to Apply
Interested and eligible candidates can apply by sending their updated resume.
Email your CV to:
๐ง hr@methicsclinical.com
Candidates who are immediate joiners will be preferred during the selection process.