Bioplus Life Sciences is a leading organization in the clinical research and pharmaceutical industry, dedicated to advancing medical research through high-quality clinical trials. With a strong focus on regulatory compliance, patient safety, and data integrity, Bioplus Life Sciences offers a dynamic work environment for professionals looking to grow in the clinical research domain.
Key Responsibilities
Clinical Trial Execution
- Coordinate daily clinical trial activities to ensure adherence to protocol timelines.
- Assist in patient recruitment, screening, and informed consent processes.
- Schedule and manage patient visits, follow-ups, and trial assessments.
- Maintain essential trial documentation, including regulatory binders, source documents, and CRFs.
Data Management & Compliance
- Ensure accurate data collection in EDC systems or paper-based CRFs.
- Support IRB submissions, amendments, and regulatory reviews.
- Liaise with sponsors, CROs, and clinical sites for smooth trial operations.
- Assist in resolving data queries and preparing for audits and inspections.
Administrative Coordination
- Track study metrics (recruitment status, data quality, compliance).
- Provide support for trial budgets, contracts, and invoicing.
Required Qualifications
- Education: BPharm / MPharm / MSc (Life Sciences, Biotechnology, Clinical Research) or BTech (Biotechnology).
- Experience: 3–4 years in clinical research coordination or related roles.
- Knowledge: Strong understanding of ICH-GCP, FDA, EMA guidelines.
- Certification: ACRP or SOCRA certification (preferred but not mandatory).
Desired Skills
✔ Strong organizational and multitasking abilities.
✔ Proficiency in EDC systems, CTMS, and MS Office.
✔ Excellent communication and interpersonal skills.
✔ Detail-oriented with strong problem-solving capabilities.
Preferred Experience
- Exposure to Phase I–IV clinical trials.
- Prior experience in hospitals, CROs, or academic research settings.
- Familiarity with clinical regulatory and ethical guidelines.
Working Conditions
- Occasional travel to clinical sites or sponsor meetings.
- Flexible hours based on trial requirements.
- Patient interaction may be required.
How to Apply for Clinical Trial Coordinator Job at Bioplus Life Sciences?
📩 Send your updated resume to: talent2@bioplus.in
