Arcolab is a leading player in pharmaceutical research, clinical trials, and pharmacovigilance (PV), committed to patient safety and regulatory excellence. With a strong presence in Bangalore, we specialize in drug safety monitoring, signal detection, and compliance assurance for global healthcare standards.
🔬 Why Join Us?
✔ Work with top industry experts in PV & clinical research
✔ Growth-oriented environment with continuous learning
✔ Competitive salary & benefits
✔ Work from Office (Bangalore) with a collaborative culture
🔥 Current Job Openings
1. Signal & Aggregate Reports Specialist
📍 Location: Bangalore (Work from Office)
🎓 Qualification: B.Pharm / M.Pharm / Pharm.D / BDS
💼 Experience: 2-5 years
Key Responsibilities:
✔ Authoring Signal Detection Reports for medicinal products
✔ Using statistical & data mining techniques to identify safety trends
✔ Generating line listings from safety databases
✔ Reviewing literature & regulatory websites for new safety data
✔ Drafting aggregate reports (PBRERs, PSURs, DSURs) as per regulations
Skills Required:
✔ Strong pharmacovigilance & signal management knowledge
✔ Experience with safety databases (Argus, ARISg, VigiFlow)
✔ Familiarity with MedDRA, WHO-DD, ICH guidelines
✔ Excellent medical writing & analytical skills
2. Compliance & Assurance Specialist (Clinical Trials/BA/BE/PV)
📍 Location: Bangalore
💼 Experience: 2-5 years
Key Responsibilities:
✔ Support Quality Management System (QMS) for clinical trials
✔ Monitor compliance in BA/BE studies & PV operations
✔ Assist in SOP creation & regulatory audits
✔ Track compliance trends & risk assessments
Skills Required:
✔ Knowledge of GCP, GLP, ICH-GCP, and pharmacovigilance regulations
✔ Experience in clinical trial compliance & audits
✔ Strong communication & problem-solving skills
3. Medical Reviewer – Pharmacovigilance (MBBS/MD)
📍 Location: Bangalore
🎓 Qualification: MBBS / MD
💼 Experience: 1-3 years
Key Responsibilities:
✔ Medical review of ICSRs (clinical trials, spontaneous reports, literature)
✔ Causality assessment & signal detection
✔ Ensure timely regulatory reporting (E2B, CIOMS, MedWatch)
Skills Required:
✔ Experience in safety databases (Argus, ARISg)
✔ Knowledge of MedDRA, WHO-DD, ICH guidelines
✔ Strong clinical & analytical reasoning
✅ Eligibility & Benefits
✔ For PV Roles: B.Pharm/M.Pharm with 2-5 years in signal management
✔ For Medical Reviewer: MBBS/MD with 1-3 years in ICSR review
✔ For Compliance Roles: Experience in GxP, clinical audits, and PV compliance
✨ Employee Benefits:
✔ Competitive salary & performance bonuses
✔ Health insurance & wellness programs
✔ Continuous training & career growth
✔ Flexible yet structured work environment
📩 How to Apply?
Interested candidates can share their updated CV to ➡ dev.kiran@arcolab.com
📌 Subject Line: “Application for [Job Title] – [Your Name]”
