Intern Safety Data Specialist

Job Description

Job Description

The Intern Safety Data Specialist (SDS-Intern) is responsible for processing adverse events (AE) information in the global safety system for investigational products, under the direction and supervision of a Global Pharmacovigilance Case Management (GPVCM) Manager. The SDS-Intern performs triage, analysis and interpretation of AE data following our Company Standard Operating Procedures (SOPs) and guidelines. In addition, the SDS-Intern collaborates with other staff within the organization, as well as cross-functionally.

Responsibilities and Primary Activities (may include but are not limited to)

• Through daily case prioritization activities, completes reports within the established timeframes to ensure compliance with internal, business partner (BP), and regulatory agency reporting requirements worldwide.
• Participates in training and certification activities for GPVCM.

Education And Other Qualifications

• University degree (bachelor or master) in the field of pharmacy, nursing, veterinary medicine, obstetrics, medical analytics, physiotherapy, medical biology, biotechnology,
• Very good written and spoken English language (B2-C1 level), particularly in usage of medical terminology (verified during interview);
• Very good written and spoken Polish; knowledge of Italian, French or German will be an additional asset;
• Computer literacy and ease of learning new computer systems and applications;
• High level of organizational skills, ability to comply with procedures, good time management and ability to effectively establish priorities;
• Ability to solve problems and work independently, competency in analytical skills and orientation to detail, openness to feedback and commitment to applying it in work

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):

Required Skills:

Adaptability, Biopharmaceutics, Biotechnology, Clinical Data Cleaning, Clinical Data Management, Customer-Focused, Data Analysis, Database Development, Data Processing, Data Quality Assurance, Data Review, Data Validation, Data Visualization, Electronic Data Capture (EDC), Italian Language, Learning Agility, Medical Terminology, Mycology, Neuroethics, Obstetrics, Pharmacology, Pharmacovigilance, PL/SQL (Programming Language), Regulatory Compliance, Veterinary Medicine

Preferred Skills:

Job Posting End Date:

10/10/2025

• 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:R363086