Job Title: Clinical Trial Assistant
Company: Forward Life Pvt. Ltd.
Location: Hyderabad
Salary: ₹18,000 – ₹22,000 per month
Working Hours: Day shift with possible rotational shifts
Industry: Clinical Research Organization (CRO)
Eligibility
- Qualification: Doctor of Pharmacy (Pharm. D) – Required
- Experience: Freshers or candidates with up to 1 year of experience in clinical research or the healthcare industry are welcome to apply
- Availability: Candidates who can join immediately will be given priority
- Commitment: Willingness to work under a long-term employment agreement (2 years)
- Shift Flexibility: Should be open to rotational shifts as required by project needs
Role Overview
The Clinical Trial Assistant will support clinical research operations including trial coordination, documentation, monitoring, and compliance. The role requires strong attention to detail, organizational skills, and the ability to collaborate with cross-functional teams while ensuring adherence to Good Clinical Practice (GCP), SOPs, and regulatory guidelines.
Key Responsibilities
1. Clinical Trial Coordination & Documentation
- Assist in preparing and maintaining clinical trial documentation such as study protocols, investigator brochures, informed consent forms, and essential trial files.
- Support coordination between clinical research sites and project teams to ensure smooth operations.
- Track trial progress including recruitment, data collection, and regulatory submissions.
- Assist in managing trial logistics, supplies, and trial data entry.
2. Compliance & Quality Management
- Ensure adherence to GCP, SOPs, and regulatory guidelines.
- Support audits, inspections, and internal reviews by maintaining accurate trial records and reports.
- Collaborate with clinical, regulatory, data management, and quality teams to ensure compliance and timely deliverables.
3. Communication & Cross-Functional Support
- Act as a liaison between clinical teams, stakeholders, and management.
- Provide support to other divisions or departments when required.
- Ensure timely follow-ups on pending tasks while maintaining professionalism and confidentiality.
4. Reporting & Data Management
- Maintain trackers, reports, and clinical trial logs for monitoring and reporting.
- Assist in preparing presentations, summaries, and status updates for management.
Required Skills & Competencies
- Understanding of clinical trial processes, documentation, and protocols
- Strong organizational and problem-solving skills
- Excellent written and verbal communication skills
- Ability to work independently and collaboratively within a team
- Proficiency in MS Office and basic data management tools
- High attention to detail and adherence to timelines and protocols
- Professionalism, discipline, and flexibility to work in shifts
Work Location: In person (Hyderabad)
Job Type: Full-time, Permanent
Benefits:
- Health insurance
- Provident Fund
Work Location: In person
Benefits:
Work Location: In person
Pay: ₹18,000.00 - ₹22,000.00 per month
Benefits:
Work Location: In person
