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Job Description

  • Perform medical review of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs), including analysis of narrative content, coding, expectedness, seriousness, causality, and company summary to meet service level agreements and regulatory timelines.
  • Edit and medically reviewAnalyses of Similar Events (AOSE)for expedited cases as required by regulatory guidelines.
  • Serve as an internal expert and consultant for the pharmacovigilance case processing teams.
  • Safety Data Analysis
  • Maintain a deep understanding of the scientific basis for therapies, drug-induced diseases, medical devices, vaccines, and the drug development process.
  • Continuously acquire and maintain knowledge of product safety profiles across therapeutic areas and the corresponding regulatory requirements.
  • Conduct process improvement activities, including the implementation of quality control processes and providing feedback to case processors on discrepancies or errors.
  • Training and Mentoring
  • Support training and mentoring for case processing/medical review personnel as required.
  • Actively contribute to the organization s initiatives to meet business and regulatory objectives.
  • Regulatory Compliance
  • Ensure compliance with international regulatory guidelines, includingFDA,ICH GCP,MHRA,PMDA, andEU Clinical Trial Directive.
  • Stay informed on medical safety and regulatory industry developments to ensure adherence to changing standards.

Job Expectations

  • Travel: Less than 5%
  • Hours: 45 hours per week
  • This position may include additional duties as assigned.

Education and Experience

  • Required Qualifications:
  • MBBS, MD, BDS, or MDS degree.
  • 1-2 years of experience as a Medical Reviewer for ICSRs in the pharmaceutical, biotech, or medical device industries. CRO experience is highly desirable.
  • Skills and Knowledge:
  • Strong understanding of pharmacovigilance regulations, including expertise in international guidelines (FDA, ICH GCP, MHRA, PMDA, GVP, EU Clinical Trial Directive).
  • Excellent interpersonal, organizational, and communication skills (both written and verbal).
  • Proficiency in MS Office applications (Outlook, Excel, Word, PowerPoint).

Cultural Beliefs at EVERSANA

  • Patient Minded: We act with the patient s best interest in mind.
  • Client Delight: We own every client experience and its impact on results.
  • Take Action: We are empowered and empower others to act now.
  • Grow Talent: We own our development and invest in the development of others.
  • Win Together: We passionately connect with anyone, anywhere, anytime to achieve results.
  • Communication Matters: We create transparent, thoughtful, and timely dialogue.
  • Embrace Diversity: We create an environment of awareness and respect.
  • Always Innovate: We are bold and creative in everything we do

More Info

Job Type:
Industry:
Employment Type:
Open to candidates from:
Indian

About Company

Thepharmadaily is the best Pharma training institute located in India, exclusively designed and fabricated for Pharmacy undergraduates & postgraduates. ThePharmadaily is here to provide Classroom training, 100% Placement assistance, Talk shows with Industry experts, interaction with experienced professionals, and real-time corporate life experiences. Thepharmadaily provides a variety of trainings like Pharmacovigilance, clinical data management, medical coding, medical writing, narrative writing, HEOR, and medical underwritting.

Job ID: 123766785