[Hiring] Senior Drug Safety Physician @Parexel

Role Description

Senior Physician, Patient Safety performs medical, safety monitoring or pharmacovigilance activities for assigned projects. They provide medical reviews, analysis and guidance in all required safety reports. Senior Physician, Patient Safety will act as Subject Matter Expert in therapeutic areas and mentor junior team members while working on complex tasks requiring in-depth evaluation.

• Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines.
• Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting.
• Communicating and discussing issues related to review process with Line Manager/ Project Leader/Designee.
• Interacting with internal and external stakeholders for resolving issues.
• Attending and/or presenting at client/cross functional meetings along with other stakeholders. Working as Subject Matter Experts (SMEs).
• Assisting the Project Lead/Functional Lead for audits and inspections.
• Providing inputs for process improvements.
• Working closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process.
• Functioning as pharmacovigilance representative/safety scientist.
• Attending/supporting Bid defense meetings.
• Actively mentoring Patient Safety Physicians to develop their skills and expertise.
• Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement), clinical trial, and literature cases including combination products (drug-device) according to client/Parexel Standard Operating Procedures (SOPs; as applicable) and liaising with the client, as required.

Qualifications

• Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date.
• Demonstrated success in technical proficiency and scientific creativity.
• Good knowledge of drug safety and the drug development process.
• Strong knowledge of international drug regulation including ICH GCP, GVP, and all other applicable regulations and guidelines.

Requirements

• Ability to work on complex tasks requiring in-depth evaluation.
• Ability to exercise judgment within broadly defined practices and policies.
• Good presentation and verbal/written communication skills.
• Good interpersonal skills.
• Client focused approach to work.
• Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps.
• An ability to comprehend various regulatory or client requests and be able to strategize a handling approach.
• Experience mentoring junior team members.
• A flexible attitude with respect to work assignments and new learnings.
• An ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
• An ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential.
• A willingness to work in a matrix environment and to value the importance of teamwork.

Benefits

• Opportunity to work on complex and impactful projects.
• Professional development and mentoring opportunities.
• Collaborative work environment.

Education

• Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD) / Medically qualified from an acknowledged Medical School.
• Completion of at least basic training in clinical medicine (residency, internship etc.).