Sr. Scientist, Medical Review Physician

2 weeks ago

Pasig, National Capital Region, Philippines ClinChoice Full time

Primary Responsibilities:

  • Awareness and understanding of relevant GVP modules.
  • Perform medical review of non-serious & serious ICSRs with emphasis on seriousness, 
    expectedness, causality & narrative etc. without missing on quality & compliance.
  • Experience of medical review of ICSRs received from sources such as Spontaneous, Literature, 
    Regulatory Authority, Solicited and Clinical trials.
  • Experience across multiple therapeutic areas such as Oncology, Respiratory, Immunology, 
    Neuroscience, Rare diseases etc.
  • Support triage of cases and determine seriousness and relatedness across products as assigned.
  • Review and verify appropriate selection of adverse events from source documents, assign 
    appropriate MedDRA code, assess labelling and review narrative.
  • Acquire and maintain current knowledge of product portfolio and safety profiles for products 
    across therapeutic areas. 
  • Involve in process improvement activities such as implementation of quality control process.
  • Provide medical guidance and expert opinion on the cases to the data entry associates and 
    quality reviewers to help resolve queries.
  • Identify and resolve case issues, coordinate with client therapeutic teams and within functional 
    team and manage as appropriate.
  • Maintain PV expertise, and understanding of international safety regulations and guidelines. 
  • Responsible for completing the MR activities in the safety database within the stipulated time to 
    comply with service level agreements and regulatory timelines.
  • Provide timely feedback to case processors on the errors/ discrepancies noted. 
  • Assist in training/mentoring of other case processing/medical review personnel as necessitated.
  • Adapt to different client case processing conventions and multi-task as per business needs.
  • Perform ad-hoc tasks as advised by the team lead/manager with quality and compliance as per 
    project requirement.
  • Participate in organizational activities to meet objectives suitable for the role/area of expertise.

Candidate Profile:

  • Should be a MBBS/MD with 4 - 5 years of experience as Medical Reviewer for ICSRs. 
  • Must possess thorough knowledge of ICH-GCP, relevant GVP module, 21 CFR guidelines and 
    other regulatory requirements.
  • Training and mentoring skill (GVP concepts & medical aspects such as disease condition, 
    product portfolio etc)
  • Must have hands on experience with MS Office applications (Outlook, Excel, Word, Power 
    Point etc.).

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