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Drug Safety Physician

Overview, Education, Careers Types, Skills, Career Path, Resources

Drug Safety Physicians monitor and assess drug safety, manage adverse events, and ensure regulatory compliance. They play a crucial role in pharmaceutical companies.

Average Salary

₹18,00,000

Growth

high

Satisfaction

medium

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Functional Skills

Functional Skills are essential skills that help individuals perform tasks effectively in everyday life, work, and education.

    -
    Pharmacovigilance Expertise
    -
    Medical Knowledge
    -
    Data Analysis and Interpretation
    -
    Regulatory Knowledge
    -
    Communication Skills
    -
    Critical Thinking and Problem-Solving
    -
    Clinical Trial Experience
    -
    Database Management
    -
    Risk Management
    -
    Case Report Evaluation
    -
    Medical Writing
    -
    Teamwork and Collaboration
Soft Skills

Communication, teamwork, and critical thinking to ensure seamless project execution.

    -
    Critical Thinking
    -
    Communication Skills
    -
    Attention to Detail
    -
    Problem Solving
    -
    Teamwork and Collaboration
    -
    Adaptability and Flexibility
    -
    Time Management
Technical Skills

Technical Skills are specialized abilities and knowledge needed to perform specific tasks or functions.

    -
    Pharmacovigilance Expertise
    -
    Medical Knowledge and Clinical Judgment
    -
    Regulatory Affairs Knowledge
    -
    Data Analysis and Interpretation
    -
    Communication and Collaboration
    -
    Database Management and Safety Systems
    -
    Risk Management and Mitigation Strategies
Duties and Responsiblities

Task

95%

Evaluate adverse event reports from clinical trials and post-market surveillance.

92%

Assess causality and severity of adverse drug reactions (ADRs) for regulatory reporting.

90%

Prepare and review safety documents, including safety management plans and risk assessments.

88%

Participate in signal detection activities to identify potential safety issues.

85%

Contribute to the development of risk mitigation strategies and pharmacovigilance plans.

82%

Collaborate with cross-functional teams, including clinical development and regulatory affairs.

80%

Monitor and analyze safety data from various sources to ensure patient safety.

78%

Provide medical expertise in the evaluation of safety data and risk-benefit assessments.

75%

Ensure compliance with global regulatory requirements for drug safety reporting.

72%

Conduct literature reviews to stay updated on safety profiles of pharmaceutical products.

70%

Assist in the preparation of regulatory submissions related to drug safety.

68%

Participate in audits and inspections related to pharmacovigilance activities.

Work Activities

95%

Oversee clinical trials, ensuring adherence to protocols and regulatory guidelines.

92%

Analyze safety data from clinical trials and post-market surveillance.

90%

Develop and implement risk management plans for pharmaceutical products.

88%

Prepare and submit safety reports to regulatory agencies (e.g., FDA, EMA).

85%

Identify and evaluate potential safety signals from various data sources.

82%

Review and assess adverse event reports and other medical information.

80%

Develop and maintain pharmacovigilance plans and procedures.

78%

Conduct literature reviews to stay updated on drug safety information.

75%

Manage and maintain safety databases for accurate data tracking.

72%

Communicate safety information to healthcare professionals and patients.

70%

Participate in audits and inspections by regulatory authorities.

Detailed Work Profile

Interests