Are you a medical professional with a passion for ensuring drug safety and patient well-being? Arcolab, a leading name in the pharmaceutical and life sciences industry, is hiring for the role of Medical Reviewer/Pharmacovigilance in Bengaluru. This is a full-time, permanent position ideal for candidates with 0 to 2 years of experience and an MBBS qualification. If you have a keen eye for detail and a strong understanding of pharmacovigilance, this could be the perfect opportunity for you.
Job Overview
Role: Medical Reviewer/Pharmacovigilance
Industry Type: Pharmaceutical & Life Sciences
Department: Research & Development
Location: Bengaluru
Experience: 0 to 2 years
Qualification: MBBS
Key Responsibilities
As a Medical Reviewer/Pharmacovigilance professional at Arcolab, you will play a critical role in ensuring drug safety and compliance with regulatory standards. Your primary responsibilities will include:
- Individual Case Safety Reports (ICSRs) Review:
- Conduct thorough and objective medical reviews of ICSRs received from clinical trials, spontaneous reports, and literature.
- Assess the medical relevance and causality of adverse events reported in ICSRs.
- Identify and evaluate potential safety signals and take appropriate follow-up actions.
- Ensure accurate and timely reporting of serious and non-serious adverse events to regulatory authorities.
- Safety Database Management:
- Utilize safety databases such as Argus, ARISg, or similar systems to manage and analyze safety data.
- Apply medical coding dictionaries like MedDRA and adhere to adverse event reporting standards such as ICH E2B.
- Collaboration and Communication:
- Work closely with cross-functional teams and stakeholders to ensure effective communication and collaboration.
- Provide medical expertise and insights to support pharmacovigilance activities.
Skills and Qualifications
To excel in this role, you should possess the following:
- MBBS qualification with 0 to 2 years of experience.
- Prior experience in medical review of ICSRs is preferred.
- Familiarity with safety databases like Argus or ARISg.
- Knowledge of medical coding dictionaries (e.g., MedDRA) and adverse event reporting standards (e.g., ICH E2B).
- Strong attention to detail and the ability to work with complex medical data.
- Excellent communication and interpersonal skills.
Why Join Arcolab?
Arcolab is a trusted name in the pharmaceutical and life sciences industry, known for its commitment to innovation and excellence. By joining our team, you will:
- Gain valuable experience in pharmacovigilance and drug safety.
- Work in a collaborative and supportive environment.
- Contribute to ensuring the safety and well-being of patients worldwide.
How to Apply
If you meet the qualifications and are excited about this opportunity, we encourage you to apply. Click on the “Apply” button below to submit your application.
