Clinical Trial Coordinator Job | Bioplus Life Sciences Bangalore
- Accelerate Your Clinical Research Career with Bioplus Life Sciences
- Key Responsibilities
- Clinical Trial Execution
- Data Management & Compliance
- Administrative Coordination
- Required Qualifications
- Desired Skills
- Preferred Experience
- Working Conditions
- How to Apply
- Job Summary Table
Clinical Trial Coordinator Job in Bangalore | Apply Now at Bioplus Life Sciences
Bioplus Life Sciences is hiring experienced Clinical Trial Coordinators in Whitefield, Bangalore. Candidates with BPharm, MPharm, MSc Life Sciences, Clinical Research, or BTech Biotechnology qualifications and 3–4 years of experience in clinical research coordination are invited to apply.
Accelerate Your Clinical Research Career with Bioplus Life Sciences
Are you passionate about clinical research and ensuring trial success? Join Bioplus Life Sciences as a Clinical Trial Coordinator and play a pivotal role in managing patient recruitment, trial documentation, and regulatory compliance.
Located in Whitefield, Bangalore, this full-time role is designed for candidates who bring strong clinical trial coordination experience and a keen understanding of GCP, ICH, and regulatory requirements (e.g., FDA, EMA).
Key Responsibilities
Clinical Trial Execution
- Coordinate day-to-day activities of clinical trials to ensure compliance with protocol timelines.
- Assist in subject recruitment, screening, and informed consent process.
- Schedule and manage patient visits, follow-ups, and assessments.
- Maintain essential study documents such as regulatory binders, source documents, and CRFs.
Data Management & Compliance
- Ensure accurate and timely data collection in EDC systems or paper-based CRFs.
- Support IRB submissions, amendments, and continuing reviews.
- Handle communication with sponsors, CROs, monitors, and clinical sites.
- Assist in resolving data queries and preparing for audits.
Administrative Coordination
- Track study metrics such as recruitment status and data quality.
- Provide administrative support for trial budgets, invoices, and contracts.
Required Qualifications
- Education: BPharm, MPharm, MSc in Life Sciences/Biotechnology/Clinical Research, or BTech in Biotechnology
- Experience: 3–4 years in clinical research or clinical trial coordination
- Strong working knowledge of ICH-GCP guidelines and regulatory standards
- Certification in Clinical Research (e.g., ACRP or SOCRA) is a plus
Desired Skills
- Exceptional organizational and multitasking skills
- Proficient in EDC systems, CTMS, and Microsoft Office Suite
- Strong communication and interpersonal abilities
- Attention to detail with effective problem-solving skills
Preferred Experience
- Exposure to Phase I–IV clinical trials
- Prior experience in hospital, CRO, or academic clinical settings
- Knowledge of clinical regulatory and ethical guidelines
Working Conditions
- Occasional travel to clinical trial sites or sponsor meetings
- Flexible working hours based on study requirements
- May involve direct patient interaction
How to Apply
Interested candidates can email their updated resumes to talent2@bioplus.in.
Take the next step in your clinical research career with Bioplus Life Sciences – a trusted name in global healthcare innovation.
Job Summary Table
| Company Name | Current Vacancies in Departments |
|---|---|
| Bioplus Life Sciences | Clinical Research / Clinical Operations |
| Required Education | Experience Required |
|---|---|
| BPharm / MPharm / MSc Life Sciences / BTech Biotechnology | 3–4 Years |
Clinical Trial Coordinator vacancy at Bioplus Life Sciences, Whitefield Bangalore for BPharm, MPharm, MSc, BTech graduates with 3-4 years of experience.
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