Live opening · Posted 11 days ago

Drug Safety Physician/Senior Drug Safety Physician

CONTINUUM India LLP · Chandigarh, Chandigarh, India (Remote)
Linkedin No
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At a glance

The key details from the original listing.

Posted 11 days ago
CompanyCONTINUUM India LLP
LocationChandigarh, Chandigarh, India (Remote)
Work modeNo
SourceLinkedin
ListedPosted 11 days ago

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About the role

Description supplied by the original job listing.

Company Description CONTINUUM India LLP is a contract research organization providing integrated services across Pharmacovigilance, Regulatory, Clinical, and Technology domains. The company supports the planning, launch, and lifecycle management of pharmaceutical products and medical devices for global clients. With a strong focus on accuracy, on-time delivery, and efficiency, CONTINUUM is committed to delivering high-quality outcomes. Its team includes experienced physicians, life science professionals, and technology experts who bring decades of cumulative client-delivery expertise. The organization offers a collaborative environment for professionals seeking to advance their careers in drug safety and related fields.
Role Description This is a full-time remote role for a Drug Safety Physician at CONTINUUM India LLP. The Drug Safety Physician will review, evaluate, and interpret safety data from clinical trials and post-marketing sources, ensuring accurate medical assessment of adverse events. The role involves preparing and reviewing safety reports, case narratives, risk–benefit assessments, and regulatory submissions in line with global pharmacovigilance requirements. The physician will collaborate with cross-functional teams.
Qualifications
Clinical and medical expertise: Medical degree (MBBS or equivalent; MD or equivalent and experience in drug safety, pharmacovigilance is mandatory
Pharmacovigilance and regulatory skills: Knowledge of global PV regulations and guidelines (e.g., ICH, EMA, FDA), experience in adverse event case review, signal detection, risk–benefit evaluation, and safety reporting.
Analytical and research capabilities: Strong skills in data interpretation, medical literature review, clinical trial safety assessment, and evidence-based decision-making.
Communication and documentation: Ability to draft clear, concise medical assessments, safety narratives, risk management documents, and regulatory reports; strong written and verbal communication skills in English.
Collaboration and remote work skills: Ability to work effectively in cross-functional, virtual teams; strong organizational skills, attention to detail, and comfort with remote work tools and digital workflows.
Technical proficiency: Familiarity with safety databases, electronic medical records, and standard office software; experience with PV or clinical systems is an advantage.
Professional attributes: Commitment to quality and timelines, ethical decision-making, continuous learning, and a structured, detail-oriented approach to drug safety activities.

Work arrangement
No

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