Global Pharmacovigilance Data Specialist - Trilingual MSD LATAM Bogota, D.C., Capital District, Colombia Join or sign in to find your next job Join to apply for the Global Pharmacovigilance Data Specialist - Trilingual role at MSD LATAM Global Pharmacovigilance Data Specialist - Trilingual MSD LATAM Bogota, D.C., Capital District, Colombia 6 days ago Be among the first 25 applicants Join to apply for the Global Pharmacovigilance Data Specialist - Trilingual role at MSD LATAM Get AI-powered advice on this job and more exclusive features. Job Description Embark on an exciting journey as our Global Pharmacovigilance Data Specialist! As a pivotal member of our global pharmacovigilance team, you'll shine in the analysis and interpretation of intricate adverse event reports from a multitude of sources and therapeutic areas. Your expertise will be crucial in ensuring our investigational and marketed products meet stringent safety standards. In this dynamic role, you'll collaborate closely with both internal and external stakeholders to resolve complex issues and uphold process standardization. Your multilingual skills, particularly in English and second language such as French, German, Portuguese or Italian will be instrumental in translating critical adverse event reports. Job Description Embark on an exciting journey as our Global Pharmacovigilance Data Specialist! As a pivotal member of our global pharmacovigilance team, you'll shine in the analysis and interpretation of intricate adverse event reports from a multitude of sources and therapeutic areas. Your expertise will be crucial in ensuring our investigational and marketed products meet stringent safety standards. In this dynamic role, you'll collaborate closely with both internal and external stakeholders to resolve complex issues and uphold process standardization. Your multilingual skills, particularly in English and second language such as French, German, Portuguese or Italian will be instrumental in translating critical adverse event reports. You will be responsible for Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, processes, and regulatory guidelines. Providing support in written translation of adverse events reports from different countries Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements. Supporting simplification and optimization of case management activities to enhance overall effectiveness. Education And Other Qualifications Bachelor’s degree or above in health care or life sciences disciplines (Nurse, Veterinary, Pharmacist, Bacteriologist or Biologist/Microbiologist). English Advanced (C1) proficiency or Intermediate B2 with C1 level in writing and reading. A certificate or diploma verifying this level will be required. Upper Intermediate to Advanced proficiency in one of the following languages is a must French, German, Portuguese, Italian. A certificate or diploma to confirm their proficiency level. At least one year of laboral experience is required. Clinical and/or Pharmacovigilance-related experience is desired. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Project Temps (Fixed Term) Relocation No relocation VISA Sponsorship No Travel Requirements No Travel Required Flexible Work Arrangements Hybrid Shift Not Indicated Valid Driving License No Hazardous Material(s) no Job Posting End Date 05/9/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R341684 Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Research, Science, and Health Care Provider Industries Biotechnology Research, Pharmaceutical Manufacturing, and Veterinary Services Referrals increase your chances of interviewing at MSD LATAM by 2x Sign in to set job alerts for “Drug Safety Specialist” roles. We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr