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Pharmacovigilance Senior Specialist (Sme) - 100% Remote, Based In India

0-2 years
Not Disclosed
10 Dec. 24, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Senior Specialist

Location: 100% Remote (India)
Contract Type: 9-Month Temporary Contract (with possibility of extension)
Start Date: As soon as possible
Working Hours: London business hours with some flexibility
Reporting to: Leadership team based in London


Job Purpose:

The primary responsibility of the Pharmacovigilance Senior Specialist is to support Pharmacovigilance Operations (PV Ops) with Individual Case Safety Report (ICSR) Management, ensuring compliance with internal standards and global regulatory requirements.


Key Responsibilities:

  1. Documentation and Standards Development:

    • Create, maintain, and archive written standards (e.g., SOPs, Work Instructions, Job Aids) for the ICSR Management Team.

    • Drive high-quality documentation of processes to comply with internal and external regulatory requirements.

  2. Process Improvement and Compliance:

    • Investigate root causes of identified problems and develop corrective/preventative actions (CAPAs).

    • Propose and implement process improvements for global pharmacovigilance operations.

    • Collaborate with third parties/vendors to develop and implement robust quality-driven processes in line with ICSR standards.

  3. Training and Support:

    • Provide expertise and training to Technical Associates on ICSR Management activities to enhance knowledge and skills.

  4. Subject Matter Expertise:

    • Act as a global subject matter expert for PV Operations processes, including providing input on strategy and policy decisions.

    • Author or contribute significantly to the development of written standards and process discussions.

  5. Operational Support:

    • Prioritize tasks and manage time effectively to meet business needs and deadlines.

    • Assist with queries and process discussions related to PV strategy/policy.


Education Requirements:

  • Degree in Life Sciences or a medically related field, OR equivalent experience.


Job-Related Experience:

  • Proven expertise in process development, including the creation and maintenance of written standards such as SOPs, Work Instructions, and Job Aids.

  • Strong ability to map processes and draft clear, concise written standards.

  • In-depth knowledge of and experience with pharmacovigilance systems and regulatory compliance.


Key Skills:

  • Excellent communication and technical writing skills.

  • Strong problem-solving and root cause analysis capabilities.

  • Proficiency in managing and prioritizing multiple tasks in a global matrix environment.

  • Ability to work independently and collaborate across diverse teams and time zones.


Additional Details:

  • Competitive salary.

  • Global company exposure, working alongside one of the largest pharmaceutical brands in the world.

  • Flexibility to accommodate the global nature of the organization.


Interested candidates are encouraged to apply promptly with their CV, earliest start date, and relevant qualifications.

For further information, please contact:
Alphanumeric Hiring Team