Biocon Biologics Hiring Fresher for Clinical Project Assistant Role

ByPharma Hiring Hub

Biocon Biologics, a global biopharmaceutical company specializing in biosimilars and biologics, is hiring for the role of Clinical Project Assistant at its Bengaluru location. This opportunity is ideal for M.Pharm, B.Pharm, B.Sc, and M.Sc candidates with 0–2 years of experience who are looking to start or grow their career in clinical research and project coordination.

The role focuses on supporting clinical project activities, documentation management, coordination with cross‑functional teams, and ensuring smooth execution of clinical trials within a regulated environment. Candidates will gain hands‑on exposure to global clinical development processes and project operations.

This is a strong entry‑level opportunity for professionals aiming to build a long‑term career in clinical research and biopharmaceutical development within a globally recognized organization.

Biocon Biologics Career

Job Overview

  • Position: Clinical Project Assistant
  • Department: CDM
  • Location: Bengaluru
  • Experience: Fresher
  • Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc
  • Job Type: Full-Time
  • Last Date of application: Not provided

Key Responsibilities – Clinical Project Assistant

  • Administrative & Project Support: Provide general administrative support to the Clinical Operations department and assist Clinical Project Managers and Therapeutic Area Heads.
  • Clinical Trial Support: Support the Clinical Study Team (CST) with selected trial management activities from study start‑up through close‑out.
  • Work closely with clinical team members to enable timely resolution of trial‑related and clinical issues.
  • TMF / eTMF Management: Support the creation, maintenance, tracking, and filing of the Trial Master File (TMF/eTMF) throughout the study lifecycle.
  • Assist with audit and inspection preparation and support study archiving activities.
  • System & Database Coordination: Coordinate setup, access requests, and maintenance for study systems such as eTMF, EDC, and shared drives.
  • Maintain and update trial‑related data in clinical databases, coordinating with internal teams to gather required information.
  • Reporting & Documentation: Generate, compile, and format study‑related reports and data outputs as requested.
  • Review trial documents for accuracy and completeness prior to filing in TMF/eTMF.
  • Communication & Meeting Support: Support preparation and distribution of study correspondence, including agendas, meeting minutes, tracking logs, spreadsheets, and presentations.
  • Facilitate planning, organization, and execution of meetings, such as study kick‑off meetings, internal team meetings, and client meetings.
  • Document Tracking & Data Collection: Facilitate receipt, collection, tracking, and review of trial‑related documents.
  • Process data collection forms, including logging, tracking, and quality checks as required.
  • Training & Team Tracking: Maintain clinical study team lists and support training compliance and tracking for study team members.
  • Ensure all required training completion is documented and up to date.
  • Financial & Vendor Support: Review study‑related invoices, track payments, and monitor vendor trial budgets for assigned studies.
  • Additional Study Support: Provide additional support to functional teams as directed by Line Management to ensure smooth study execution.

Required Skills & Qualifications

  • Freshers and entry‑level candidates are eligible to apply.
  • Prior internship or exposure to clinical research is an advantage.
  • Skills Required
    • Basic understanding of clinical trials and clinical research processes.
    • Familiarity with TMF, eTMF, and EDC systems is a plus.
    • Strong organizational and documentation skills to manage study records effectively.
    • Good communication and coordination abilities for supporting cross‑functional clinical teams.
    • Proficiency in Microsoft Office (Word, Excel, PowerPoint) and basic data handling tools.

Why Join Biocon Biologics

  • Global Biopharmaceutical Organization
  • Be part of Biocon Biologics, a globally recognized biopharmaceutical company with a strong focus on biosimilars and biologics, supporting patients worldwide.
  • Strong Entry‑Level Opportunity
  • The Clinical Project Assistant role provides an excellent starting point for freshers and early‑career professionals to build a career in clinical research and project coordination.
  • Exposure to Global Clinical Development
  • Gain hands‑on experience supporting global clinical trials, clinical operations, and project management activities within a regulated clinical environment.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Clinical Project Assistant

1. Who can apply for the Clinical Project Assistant role at Biocon Biologics?

B.Pharm, M.Pharm, B.Sc, and M.Sc candidates with 0–2 years of experience can apply. Freshers and entry‑level professionals are encouraged.

2. Is this role suitable for freshers?

Yes. This role is designed for freshers and early‑career candidates looking to start a career in clinical research and project coordination.

3. What are the main responsibilities in this role?

You will support clinical project activities, assist Clinical Project Managers, manage TMF/eTMF documentation, coordinate meetings, maintain study systems, track training, and support trial execution from start‑up to close‑out.

4. Do I need prior clinical research experience?

Prior experience is not mandatory. However, internships or exposure to clinical research environments will be considered an advantage.

5. Will I work with TMF/eTMF and EDC systems?

Yes. You will support activities related to TMF/eTMF creation and maintenance, system access coordination, and basic EDC‑related data handling.

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