Opportunity for Manager in Drug Safety at Covance | B.Pharm, B.Sc


Covance, the drug development business of LabCorp, is recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, with our comprehensive service portfolio, you’ll have the opportunity to explore diverse projects and unique career paths across the drug development spectrum. Join us and discover your extraordinary potential.

Post : Project Manager Drug Safety

Job Description
The Drug Safety Project Manager manages specific Pharmacovigilence and Drug Safety Services operations associated with assigned products, including the entire adverse events process from trial to post marketing. You will monitor and manage the workflow for assigned projects with responsibility for making decisions regarding adverse event reporting within specific guidelines. Additional responsibilities include but are not limited to:
• Work closely with the clinical operations and project management teams to ensure all PV & DSS activities are performed according to the regulatory and contractual requirements of the study.
• Provide oversight of the receipt and processing of all adverse event reports including entry of safety data, writing patient narratives, and coding adverse events in MedDRA.
• Identify clinically significant information missing from initial reports and collect missing data
• Ensure the cases receive appropriate medical review
• Prepare follow-up correspondence consulting with the medical staff accordingly

Candidate Profile
• University degree in Biological Sciences, Pharmacy, Nursing, Life Sciences, or Chemistry preferred
• A minimum of 7 years experience in Drug Safety*
• Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions.
• Working knowledge of relevant worldwide pharmacovigilance regulations and guidelines
• Working knowledge of GCP/ICH guidelines related to clinical safety documentation
• Experience with aggregate reporting
• Awareness of the regulatory environment regarding Risk Management and Pharmacovigilance

Additional Information
Experience : 7 years
Qualification : B.Pharm, B.Sc
Location : Mumbai
Industry Type : Pharma
Functional Area : Drug Safety
End Date : 20th December, 2018


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