Skip to main content
Upload your CV and find your next job on Indeed!

Medical Search jobs

Sort by: -
    • Conduct literature searches for drug safety information.
    • Review medical records and safety data for completeness and accuracy.
  • View similar jobs with this employer
    • Contribution to healthcare: Play a vital role in ensuring reliable data that supports medical research and patient outcomes.
    • Communicate with medical experts, patients, or representatives from pharmaceutical companies for medical resources and verifications.
    • The candidate should have essential data entry skills, like fast typing with an eye for detail and familiarity with MS Office and google search.
    • How do you ensure medical accuracy and content compliance?
    • Ability to research from authoritative medical sources and simplify complex topics for patients.
    • Minimum of 2 years of experience in healthcare products or medical devices required and minimum of 1 year of previous medical writing experience in a healthcare…
    • Initial triage of regulatory authority database searches.
    • Perform Duplicate searches and complete initial book-in as required.
    • Strong knowledge of anatomy, physiology, and medical terminology.
    • With strong domain expertise in CPT and ICD (diagnosis) coding, the incumbent should be able…
    • Previous medical device consulting experience.
    • A demonstrated knowledge and understanding of global medical device regulations.
    • Support resolution of technical/medical doubts raised by team members.
    • 3-7 years of experience in regulatory/medical writing.
    • Quality Control (QC) of Documents.
    • Proven ability to conduct keyword research and optimize content for search intent.
    • Our benefits include medical insurance, accident insurance and retiral…
    • Basic working knowledge of medical device clinical and regulatory documentation.
    • Preferred: 2+ years experience in medical or regulatory writing.
    • Develop industry-leading controlled experiments that adhere to budgetary constraints and project directives.
    • Safely perform experiments on subjects, maintaining…
    • Ability to evaluate clinical safety, performance, and benefit-risk profiles of medical devices.
    • Experience in conducting clinical literature searches, appraisal…
    • To monitor the site quality system compliance requirement of Schedule M, MHRA, SAHPRA, ISO 9001 and other regulatory authorities.

Job Post Details

Pharmacovigilance Associate - job post

Cliniweb Services
Pune, Maharashtra
₹2,80,000 - ₹4,50,000 a year

Job details

Pay

  • ₹2,80,000 - ₹4,50,000 a year

Job type

  • Permanent
  • Fresher
  • Full-time

Location

Pune, Maharashtra

Benefits

Pulled from the full job description

  • Paid time off
  • Paid sick time
  • Cell phone reimbursement
  • Flexible schedule

Full job description

  • Collect and process adverse event (AE) and adverse drug reaction (ADR) reports
  • Review medical records and safety data for completeness and accuracy
  • Argus Safety
  • ARISg
  • VigiFlow
  • MedDRA
  • WHO Drug Dictionary
  • Prepare and submit Individual Case Safety Reports (ICSRs)
  • Conduct literature searches for drug safety information
  • GVP guidelines
  • FDA regulations
  • EMA guidelines
  • ICH guidelines
  • Maintain confidentiality and accurate documentation
  • Support signal detection and risk management activities
  • Coordinate with healthcare professionals and internal teams

Pay: ₹280,000.00 - ₹450,000.00 per year

Benefits:

  • Cell phone reimbursement
  • Flexible schedule
  • Paid sick time
  • Paid time off

Work Location: In person

Let Employers Find YouUpload Your Resume