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Skills

  • Pharmacovigilance
  • Reports
  • Literature
  • Management
  • Medical
  • Processing
  • Reviews
  • Analytics
  • Coding
  • Csr
  • Design
  • Inbound Marketing
  • International
  • Likes
  • Marketing

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Services

  • Medical Writing

    $15/hr Starting at $25 Ongoing

    Dedicated Resource

    Our medical writing services include clinical and regulatory writing, as well as scientific communications, education material and medical writing consultancy. Regulatory and Clinical Writing ICH GCP...

    CsrDesignMarketingMaterialsMedical
  • End to End Pharmacovigilance Services

    $30/hr Starting at $1K Ongoing

    Dedicated Resource

    Processing and management of ICSRs including Case intake, Case entry, MedDRA and WHO-DD coding, Triaging, Quality Control, Medical review etc) Generation of Regulatory reports including Expedited, PSURs,...

    AnalyticsCodingLiteratureManagementMedical
  • Pharmacovigilance LITERATURE MANAGEMENT

    $30/hr Starting at $1K Ongoing

    Dedicated Resource

    Screening and Extraction of Literature cases Monitor safety-relevant literature databases like PubMed, Medline, Embase etc. Rapidly identify adverse events from wide range of sources like: All relevant...

    Inbound MarketingInternationalLikesLiteratureManagement

About

Qualified Pharmacovigilance Professional with 8 years of experience

Sunil is a qualified MBA and Pharmacy professional with over 10 years of experience in Pharmaceutical industry especially in the areas of Pharmacovigilance and Clinical research. He was Global Clinical Pharmacovigilance Manager for ADI Group, during which he initiated the development of the company’s Pharmacovigilance quality management system for its clinical development programme. In this role, he was responsible for Pharmacovigilance, medical information and clinical development. He also has experience as consultant to develop companies core Pharmacovigilance activities for audit purpose.
Sunil has also been involved in training throughout his career particularly in the areas of Pharmacovigilance including ARGUS Safety, Clinical Research and Medical Writing. With over 10 years of experience in the pharmaceutical industry and clinical research organization, he offer his clients the assurance that their drug safety training programs are being conducted by a seasoned Pharmacovigilance executive with experience in developing, implementing and leading safety trainings in lower cost markets.
Client certified trainer – with 5 years of varied industry experience to conduct training for Pharmacovigilance processes including ARGUS Safety, MedDRA and WHO Drug Dictionary and case processing in Pharmacovigilance.

Work Terms

24X7 availability, flexible, customized solution for Clients,Online payment