Clinical Trial Assistant - Clinical Research Operations

Why This Role Matters
The Clinical Trial Assistant supports clinical research operations by assisting in trial coordination, documentation management, and compliance activities. This role contributes to maintaining high standards of clinical research while ensuring adherence to regulatory requirements and Good Clinical Practice guidelines.

Job Description
The Clinical Trial Assistant will support clinical trial activities including documentation management, coordination between research teams, and compliance monitoring. The role involves maintaining essential trial documents, tracking study progress, and assisting with regulatory and quality processes to ensure efficient clinical research operations.

Key Features of the Role
• Opportunity to begin a career in clinical research and clinical trials
• Exposure to real-time clinical trial management and coordination
• Collaborative work environment within a Clinical Research Organization
• Professional development opportunities in clinical operations
• Experience with clinical documentation and regulatory compliance

Responsibilities

Clinical Trial Coordination and Documentation
• Assist in preparing and maintaining clinical trial documents such as study protocols, investigator brochures, informed consent forms, and trial master files
• Support coordination between clinical research sites and project teams
• Track trial progress including patient recruitment, data collection, and regulatory submissions
• Assist in managing trial logistics, supplies, and data entry

Compliance and Quality Management
• Ensure compliance with clinical research standards including Good Clinical Practice (GCP) and internal SOPs
• Support audits, inspections, and internal reviews through proper documentation
• Collaborate with clinical, regulatory, data management, and quality teams to maintain compliance

Communication and Cross-Functional Support
• Act as a liaison between clinical teams, stakeholders, and management
• Support cross-departmental activities when required
• Ensure timely follow-up on assigned tasks while maintaining confidentiality and professionalism

Reporting and Data Management
• Maintain trackers, reports, and clinical trial logs
• Assist in preparing presentations, reports, and status updates for management

Required Qualifications

Educational Requirements
• Doctor of Pharmacy (Pharm.D) – Required

Experience and Skills
• Freshers or candidates with up to 1 year of experience in clinical research or healthcare
• Understanding of clinical trial documentation and research processes
• Strong organizational and time management skills
• Excellent written and verbal communication skills
• Proficiency in Microsoft Office and basic data management tools
• Ability to work independently and collaboratively in teams
• Strong attention to detail and adherence to regulatory timelines

Salary Insights
• INR 22,000 – INR 25,000 per month

Work Schedule
• Day shift with possible rotational shifts

Benefits
• Health Insurance
• Provident Fund
• Exposure to clinical trial operations and regulatory processes
• Structured learning opportunities in clinical research

Company Overview
Forward Life Pvt. Ltd. operates within the clinical research sector, supporting clinical trials and research programs through coordination, compliance management, and data oversight. The company provides professionals with opportunities to gain practical exposure to clinical trial operations and regulatory processes in a collaborative environment.

FAQs
• What qualification is required for this role?
Candidates must have completed a Pharm.D degree.

• Is prior experience required?
Freshers and candidates with up to one year of experience can apply.

• What is the salary range for this role?
The salary ranges from INR 22,000 to INR 25,000 per month.

• Where is the job located?
The role is based in Ameerpet, Hyderabad, Telangana.

Application Tips
• Highlight coursework or training related to clinical research
• Mention knowledge of clinical trial documentation and GCP guidelines
• Include any internship or project experience in healthcare or research
• Emphasise organizational and communication skills
• Structure clinical research knowledge clearly in your resume