Inactive
M

Merck

Makes medicines, vaccines and animal treatments

Associate Specialist - Drug Safety

Regulatory & Quality (Life Sciences)Posted on Oct 15
Full-timeJakarta, IndonesiaNo salary listed

About the Job

Requirements

  • A health, life science, or medical science degree, or equivalent education/experience, subject to hiring-manager discretion.
  • General knowledge of adverse-event reporting requirements and relevant pharmacovigilance regulations.
  • Fluency in written and spoken English and proficiency in the local language.
  • Experience in the pharmaceutical industry is preferred, subject to hiring-manager discretion.
  • Communication, organizational, and time-management skills.

Responsibilities

  • Assist with execution of local pharmacovigilance processes and activities in collaboration with internal functional areas and external parties, including local pharmacovigilance agreements, due diligence, Post-approval Safety Monitoring Program implementation, and scheduling and submission of aggregate safety reports.
  • Assist with day-to-day adverse-event case management, which may include case intake, translation into or from English and/or the local language, acknowledgments, follow-up, and submissions in accordance with procedures and country regulations.
  • Support local pharmacovigilance audits and inspections when requested.
  • Participate in issue-management and compliance activities and assist in coordinating and preparing local corrective actions.
  • Support development and maintenance of local pharmacovigilance procedures and controlled documents.
  • Support pharmacovigilance self-inspections required by applicable legislation.
  • Support local implementation and oversight of Risk Minimization Measures and Additional Risk Minimization Measures in accordance with local procedures and legislation.
  • As applicable, manage and perform local literature screening and assessment in accordance with company procedures and local requirements.
  • Support local implementation of applicable business continuity plans.
  • Translate or quality-check translations of applicable pharmacovigilance documents.
  • File, store, and archive safety-related documentation in accordance with company policies and local requirements.
  • Participate in special projects or rotational assignments within or outside of International Pharmacovigilance as part of professional development.
  • Complete all required and applicable training assigned at or after hire by the due dates and before performing the relevant activities.

Desired Qualifications

  • Experience in the pharmaceutical industry.

About the Company

Merck

Makes medicines, vaccines and animal treatments

Merck develops prescription medicines, vaccines and veterinary treatments for patients, health systems and animal owners worldwide. Its vaccine portfolio includes Gardasil 9, which helps prevent cancers and other diseases caused by several types of human papillomavirus. The company takes potential treatments through laboratory research and clinical trials, then manufactures and sells approved products to drug distributors, hospitals, physicians and governments. Its animal health division sells medicines and vaccines to veterinarians, farmers and pet owners, while selected drug partnerships also earn shared profits or royalties. Founded in 1891, Merck is headquartered in Rahway, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Rahway, NJ
Founded
1891

Recently Posted Jobs

Explore more opportunities at Merck

See more jobs