Drug Safety Physician

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Job Purpose: 

• Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational and marketed products
• Signal detection/analysis/evaluation and ongoing safety surveillance activities
• Provide medical guidance and input to Drug Safety associates (DSAs) and specialists in medical aspects of drug safety
• Function as pharmacovigilance representative/safety scientist

General

• Maintaining a good working knowledge of the Adverse event profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and international drug safety regulations 
• Maintaining an awareness of global regulatory requirements and reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
• Maintaining excellent knowledge of the safety profile of assigned products
• Communicating and discussing issues related to review process with Project Manager
• Interacting with internal and external contacts for resolving issues
• Maintaining a good working knowledge of relevant regulatory guidelines
• Attend and present client/cross functional meetings along with other stakeholders

Case report Medical review

• Performing medical review of cases according to client Standard Operating Procedures (SOPs) and liaising with the client, as required
• Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
• Assessing seriousness and expectedness of reported events
• Providing medical advice to case processing team

Skills:

• Excellent interpersonal, verbal and written communication skills
• Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system
• Client focused approach to work
• A flexible attitude with respect to work assignments and new learnings
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential
• Willingness to work in a matrix environment and to value the importance of teamwork
• Strong knowledge of international drug regulation including GCP, GVP

Knowledge and Experience:

Good knowledge of medical terminology.

Fresher/ relevant experience into pharmacovigilance/ Drug Safety field is preferred. 

Education:

MBBS/MD

Experience Level

Mid Level