[Hiring] Drug Safety Physician @Parexel

Role Description

We are seeking a Drug Safety Physician to join our team in Remote capacity. As a Drug Safety Physician, you will play an important role in supporting pharmacovigilance and drug safety activities that help protect patient safety throughout the product lifecycle. This position contributes to medical review, safety surveillance, aggregate reporting, signal management, literature review, and medical monitoring activities across clinical development and post-marketing programs.

You will collaborate with cross-functional teams, clients, and stakeholders to evaluate safety information, ensure compliance with global pharmacovigilance requirements, and support timely safety reporting. Responsibilities include:

• Medical review of adverse event cases.
• Provision of medical guidance to safety teams.
• Support for regulatory safety documentation.
• Contribution to signal detection and management activities.

You'll join a fast-paced, growth-oriented environment focused on advancing patient safety, supporting regulatory compliance, and strengthening evidence-based decision making.

Qualifications

• Strengths in medical review, clinical assessment, and scientific communication.
• Experience working in clinical medicine, pharmacovigilance, clinical research, or a regulated healthcare environment.
• The ability to collaborate across teams and communicate clearly with internal and external stakeholders.
• A patient-focused mindset and strong attention to detail.
• Comfort working with safety databases, web-based applications, Microsoft Office tools, and pharmacovigilance processes.

Requirements

• Bachelor of Medicine, Bachelor of Surgery (MBBS), Doctor of Medicine (MD), or equivalent medical qualification from an accredited medical school.
• Completion of basic clinical medicine training, including residency, internship, or equivalent.
• Fresher or relevant experience in pharmacovigilance, drug safety, clinical practice, or medical data review activities.
• Knowledge of medical terminology and clinical assessment principles.
• Understanding of ICH-GCP, GVP, global drug safety regulations, and applicable pharmacovigilance guidelines.
• Strong communication, organization, analytical, and problem-solving skills.
• Computer proficiency, including experience with Microsoft Office applications and web-based systems.

Preferred Qualifications

• Experience in pharmacovigilance and medical data review activities.
• Familiarity with global pharmacovigilance processes.
• Demonstrated ability to present medical information effectively and work in cross-functional environments.