Advertisement
Johnson & Johnson, a global leader in healthcare innovation and clinical research, is seeking an Associate Site Manager for its Mumbai location. This is an excellent opportunity for candidates with clinical trial monitoring, site management, and regulatory knowledge to step into a pivotal role supporting R&D operations.
Advertisement
If you have a strong background in clinical research, GCP compliance, and trial oversight, this role offers growth, impact, and career advancement in the pharmaceutical and healthcare industry.
🔹 Key Responsibilities
As an Associate Site Manager, you will:
- Act as the primary contact between Johnson & Johnson and assigned trial sites.
- Participate in site feasibility and qualification visits.
- Manage site initiation, monitoring, and close-out activities (on-site & remote).
- Ensure GCP compliance, data integrity, and regulatory adherence.
- Train and support site staff, ensuring accurate records and timely data entry.
- Oversee drug supply management, safety reporting (AE/SAE), and PQC documentation.
- Collaborate with Local Trial Managers (LTM), Clinical Trial Assistants (CTA), and Trial Delivery Leaders (TDL).
- Support site recruitment strategies and implement corrective/preventive actions (CAPA).
- Prepare trial sites for close-out visits and ensure documentation completeness.
🎓 Qualifications
- Education: BA/BS degree in Pharmacy, Nursing, Life Sciences, or related field.
- Experience:
- 1–2 years of clinical trial monitoring preferred.
- Study coordinators with 3–4 years of relevant experience are also eligible.
- Skills Required:
- Working knowledge of GCP, SOPs, and local regulations.
- Familiarity with Regulatory (eSUGAM) submission, import/export compliance.
- Proficiency in English and local language (oral & written).
- Strong IT and data management skills.
- Other: Willingness to travel occasionally, but primarily in-house site management role.
🌟 Benefits
Working with Johnson & Johnson offers:
Advertisement
- Exposure to global clinical research processes.
- Professional growth opportunities with a leading healthcare organization.
- Hybrid work model with centralised trial management responsibilities.
📌 How to Apply

Advertisement