Medical Doctor

Job Title:

Location:

Working Model:

Qualifications:

• MBBS (Medical Degree), preferably with a postgraduate qualification.
• Minimum

  2+ years of experience

  in clinical practice or pharmacovigilance (PV).
• Must hold valid

  Medical Doctor certification/licensure

  in the country of service.
• Experience in the pharmaceutical industry preferred.
• Working knowledge of

  international regulations and guidance documents

  related to worldwide reporting requirements (US/EU).

Key Responsibilities:

• Perform comprehensive

  medical review

  of cases, ensuring consistency and accuracy of information.
• Provide

  causality assessment

  and

  clinical evaluation comments

  as required.
• Support the preparation of

  clinical trial safety assessments

  ,

  regulatory submissions

  , and

  aggregate safety reports

  .
• Ensure compliance with

  pharmacovigilance regulations

  and company policies.
• Identify and resolve issues independently; escalate complex matters appropriately.
• Demonstrate strong

  analytical and decision-making skills

  in both routine and complex scenarios.
• Collaborate effectively within a

  matrix organization

  , working both independently and under supervision.
• Maintain high productivity, organization, and time management to meet regulatory compliance goals.
• Exhibit

  excellent oral and written communication

  in English.

Skills & Competencies

• Strong understanding of

  pharmacovigilance processes

  and

  safety data management

  .
• Proficiency in

  database management systems

  and computer applications.
• Excellent organizational and problem-solving skills.
• Ability to work under tight timelines while maintaining quality standards.