Biocon Biologics Hiring Clinical Project Assistant
- Biocon Biologics Hiring Clinical Project Assistant – Freshers & Entry-Level | Bengaluru Clinical Research Jobs
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Clinical Documentation & TMF Management
- Data Management & Reporting
- Coordination & Communication
- Financial & Compliance Support
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is prior experience required?
- 3. What is the career growth after this role?
- 4. What skills are important for selection?
- 5. Is this a good entry-level pharma job?
- Summary Table
Biocon Biologics Hiring Clinical Project Assistant – Freshers & Entry-Level | Bengaluru Clinical Research Jobs
Biocon Biologics is hiring Clinical Project Assistant professionals for its Clinical Operations department in Bengaluru, Karnataka. This is a full-time, on-site opportunity ideal for freshers and entry-level candidates looking to start a career in clinical research, clinical trials management, and pharmaceutical project coordination. The role supports Clinical Project Managers and study teams in managing global clinical trials efficiently.
Company Overview
Biocon Biologics is a leading global biopharmaceutical company focused on developing affordable biosimilars and innovative biologic therapies. As a subsidiary of Biocon Ltd., the company has established itself as a key player in the biotechnology and pharmaceutical industry, delivering high-quality healthcare solutions across multiple international markets.
Known for its strong R&D capabilities, regulatory excellence, and commitment to patient-centric innovation, Biocon Biologics offers professionals a solid platform to build careers in clinical research, drug development, and regulatory operations.
Job Role & Responsibilities
As a Clinical Project Assistant, you will play a crucial role in supporting clinical trial operations, documentation management, and coordination across study teams. This role is essential for ensuring smooth execution of clinical studies from initiation to close-out.
Core Responsibilities
- Provide administrative and operational support to Clinical Project Managers and Therapeutic Area Heads
- Assist clinical study teams in trial management activities from study start-up to close-out
- Coordinate with cross-functional teams to resolve clinical trial issues efficiently
Clinical Documentation & TMF Management
- Support creation and maintenance of Trial Master File (TMF/eTMF)
- Track, organize, and archive clinical trial documents for audits and inspections
- Review trial documents for completeness and accuracy before filing
Data Management & Reporting
- Maintain and update trial-related data in clinical databases such as eTMF systems
- Generate study reports, dashboards, and tracking sheets
- Process data collection forms and ensure quality control of study data
Coordination & Communication
- Organize project meetings including kickoff meetings, internal reviews, and client discussions
- Prepare meeting agendas, minutes, and presentations
- Coordinate access and maintenance of project systems like EDC and shared drives
Financial & Compliance Support
- Review study-related invoices and track vendor budgets
- Support compliance with clinical research regulations and SOPs
- Maintain clinical study team lists and training records
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in Life Sciences or related disciplines.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research, Nursing
Experience
- Freshers and entry-level candidates can apply
- Prior internship or exposure to clinical research will be an advantage
Skills Required
- Basic understanding of clinical trials and clinical research processes
- Knowledge of TMF, eTMF, and EDC systems is a plus
- Strong organizational and documentation skills
- Good communication and coordination abilities
- Proficiency in MS Office and data handling tools
Location & Salary
- Job Location: Bengaluru, Karnataka, India
- Employment Type: Full-time, On-site
- Salary: Competitive salary aligned with entry-level clinical research roles in India
Application Process
Interested candidates can apply through the official job posting link below:
Apply Here: https://www.linkedin.com/jobs/view/4388082380/
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with Life Sciences, Pharmacy, Biotechnology, or Clinical Research backgrounds can apply. Freshers are eligible.
2. Is prior experience required?
No. This role is suitable for freshers, though internships in clinical research are beneficial.
3. What is the career growth after this role?
You can progress to Clinical Research Associate (CRA), Clinical Project Coordinator, or Clinical Project Manager roles.
4. What skills are important for selection?
Attention to detail, documentation accuracy, communication skills, and basic clinical research knowledge.
5. Is this a good entry-level pharma job?
Yes. It is one of the best entry-level opportunities in clinical research and clinical trial management.
Summary Table
| Category | Details |
|---|---|
| Company | Biocon Biologics |
| Vacancies | Clinical Project Assistant |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research, Nursing |
| Experience | Freshers Eligible |
To apply for this job please visit www.linkedin.com.
