Global Pharmacovigilance Data Specialist - Bilingual at Merck Sharp & Dohme Corp. /Netherlands

Guaduas, Cundinamarca, Colombia -

Full Time

Start Date

Immediate

Expiry Date

21 Feb, 26

Salary

0.0

Posted On

23 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Adaptability, Business Data Analytics, Clinical Data Cleaning, Clinical Data Management, Communication, Customer-Focused, Data Analysis, Data Quality Assurance, Data Review, Data Validation, Data Visualization, Electronic Data Capture, Learning Agility, Pharmacovigilance, Process Management, Safety Management

Industry

Pharmaceutical Manufacturing

Description

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 bilingual skills in English 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. • At least one year of laboral experience is required. Clinical and/or Pharmacovigilance-related experience is desired Required Skills: Adaptability, Business Data Analytics, Clinical Data Cleaning, Clinical Data Management, Communication, Customer-Focused, Data Analysis, Database Development, Data Processing, Data Quality Assurance, Data Review, Data Science, Data Validation, Data Visualization, Electronic Data Capture (EDC), Learning Agility, Periodic Safety Update Reports, Pharmacovigilance, PL/SQL (Programming Language), Process Control, Process Management, Process Safety, Safety Management, Safety Procedures Preferred Skills: 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: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Job Posting End Date: 11/28/2025 *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:R372028

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Responsibilities

You will analyze and interpret adverse event reports from various sources and therapeutic areas, ensuring compliance with safety standards. Collaboration with stakeholders to resolve complex issues and support process standardization will be key aspects of your role.