Safety Data Lead I at Merck Sharp & Dohme Corp. /Netherlands

, , China -

Full Time

Start Date

Immediate

Expiry Date

06 Mar, 26

Salary

0.0

Posted On

06 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Adverse Events, Case Management, Clinical Data Management, Clinical Knowledge, Compliance Reporting, Data Analysis, Data Processing, Process Standardization, Regulatory Compliance, Regulatory Requirements, English Language, Japanese Language, Translations

Industry

Pharmaceutical Manufacturing

Description

Job Description The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Manager in the Global Pharmacovigilance Case Management (GPVCM), the Safety Data Lead executes AE case management activities for both investigational and marketed products in accordance with specific therapeutic area standards. Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes. Among other tasks, the Safety Data Lead is 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, GPVCM processes and regulatory guidelines. Providing support or leading operational activities appropriate to level of experience and expertise. 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. Advanced writing/reading and intermediate speaking/listening English language skills. Optional advanced writing/reading and intermediate speaking/listening other region-specific language skills. Understanding of pharmacovigilance-related regulations is desired. Core Competencies: Decision Making: identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitive and qualitive information; choosing the best course of action by establishing clear decision criteria, generating, and evaluating alternatives, and making timely decisions. Business Savviness: understanding the business; building and applying knowledge of company and functional area operations, to improve individual, work group and/or organizational results. Networking & Partnerships: building partnerships; developing and leveraging relationships within and across work groups to achieve results. Strategic Planning: prioritizing and planning; establishing an action plan for self and others to complete work efficiently and on time by setting priorities, establishing timelines, and leveraging resources. Motivation and Inspiration: Communicating effectively; conveying information and ideas clearly and concisely to individuals or groups in an engaging manner that helps them understand and retain the message; listening actively to others. R377137 #Global Data Management Standard Required Skills: Adverse Events, Case Management, Clinical Data Management, Clinical Knowledge, Compliance Reporting, Data Analysis, Data Processing, Process Standardization, Regulatory Compliance, Regulatory Requirements Preferred Skills: English Language, Japanese Language, Translations 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: 06/30/2026 *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. Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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Responsibilities

The Safety Data Lead is responsible for analyzing and interpreting adverse experience reports while ensuring compliance with regulatory requirements. This role involves collaboration with stakeholders to maintain high-quality execution of case management activities.