
Pharmacovigilance Expert
4 days ago
We are seeking a highly skilled Medical Reviewer to join our team.
The ideal candidate will have a strong background in pharmacovigilance and excellent communication skills.
- Key Responsibilities:
- Proficient in post-marketing drug safety and medical review of ICSRs (Spontaneous, literature, clinical studies).
- Support seriousness assessment, initial triage, causality, medical assessment, and benefit-risk evaluation of medicinal products.
- Perform additional reviews to ensure competency and participate in audits and inspections as required.
- Understand client needs, conventions, and meet/exceed expectations through effective training and mentoring of team members on good case assessment and MedDRA coding.
- MBBS or MD degree.
- 3-4 years of experience working for service providers or pharmaceutical companies in the Pharmacovigilance department.
- Excellent communication skills, written and verbal, to explain complex concepts and address queries from the team.
- Clinical experience is an advantage, along with emotional intelligence, adaptability, analytical skills, flexibility, reliability, strong organization skills, punctuality, database experience, and ability to deliver constructive feedback.
The successful candidate will be able to apply pharmacovigilance principles effectively in a fast-paced environment and possess a deep understanding of the field.
-
Senior Clinical Pharmacovigilance Advisor
2 days ago
Mysore, Karnataka, India beBeeClinical Full time ₹ 40,00,000 - ₹ 50,00,000Job OpportunityWe are seeking an experienced medical professional to lead our clinical and pharmacovigilance team. The successful candidate will have extensive experience in leading medical review teams, client communications, and safety database management.Clinical Phase Responsibilities:Medical Oversight: Lead as a medical monitor/Medical expert and ensure...
-
Medical Writer
4 days ago
Mysore, India Sitero LLC Full time**DESCRIPTION**: The individual will be an integral part of a group of safety professionals within Sitero and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations,...