Senior Specialist, Drug Safety

Msd; Warszawa; Hybrid; PLN 180.000 - 240.000; Vollzeit

Zusammenfassung

MSD in Warsaw is seeking a Senior Specialist, Drug Safety to lead PV processes and ensure high-quality adverse event reporting. You will develop, maintain, and audit processes, collaborate with internal and external stakeholders, and support SDLC activities for compliant PV systems.

The role requires a life sciences degree and at least two years in pharmacovigilance, with strong leadership and communication skills. Hybrid work arrangement is offered, with relocation if needed.

Qualifikationen

• Bachelor's degree or master's degree in life science/health care/pharmaceutical related field.
• At least two years of pharmacovigilance safety experience or related areas such as Clinical Risk Management, Clinical or Regulatory.
• Strong knowledge base of pharmacovigilance principles with close attention to detail and ability to be flexible to meet daily competing priorities of the business.
• Demonstrates leadership, and excellent communication and interpersonal skills.
• Ability to manage and independently drive projects to completion.

Aufgaben

• Lead the development of processes with internal and external stakeholders to ensure quality and compliance of individual adverse experience case and periodic reports.
• Provide expert guidance and perform safety system configuration update and maintenance activities to ensure compliant case data handling as part of the end-to-end ICSR lifecycle: Study Configuration, Product Configuration, Reporting Destinations, Reportability Rules and Label Validation Files.
• Support Safety System Development Lifecycle (SDLC) activities to ensure these systems remain compliant with both internal and external requirements and pursue process efficiencies.
• Provide content for the ongoing development and expert review of the Global Safety Database User Manual, SOPs, and training material as needed to ensure accuracy.
• Provide expert guidance on the PV activities outlined by procedures (SOPs, User Manual, etc.).
• Responsible for drafting, negotiation, and maintenance of PV agreements and safety management plans.
• Identify and prioritize PV agreements and safety management plans to maintain compliance with worldwide regulatory requirements.
• Responsible for the end-to-end GCS&PV implementation and maintenance for select business deals.
• Support due diligence and qualification activities for selecting partner deals/projects.
• Interact closely with the business system owner for the maintenance of the Business Development Lifecycle Management system.
• Perform quality review of expedited and periodic reports to ensure adherence to global case processing standards and regulatory requirements.
• Identify, prioritize, and monitor quality issues to be resolved to maintain compliance.
• Lead efforts to improve departmental efficiencies and continuous improvement.
• Process incoming communications from internal and external sources and initiate appropriate course of action and/or response.
• Monitor group mailboxes utilized for the centralization of process/subject specific inquiries.
• Assist in preparing and responding to Regulatory Agency Inspections as well as internal and external audits.
• Follow company always polices and legal guidelines.
• Develop and support processes that facilitate achievement of GCS&PV objectives.
• Support any other project or perform any other task deemed appropriate by management.

Kenntnisse

Adverse Event Report

Auditing

Compliance Monitoring

Data Analysis

Drug Safety Surveillance

Pharmaceutical Regulatory Compliance

Pharmacovigilance

Process Improvements

Quality Compliance

Quality Control Management

Quality Reporting

Regulatory Audits

Regulatory Compliance

Regulatory Inspections

Regulatory Reporting

Regulatory Requirements

Regulatory Reviews

Risk Management

Safety Management

Ausbildung

Bachelor's or Master's degree in life science/health care/pharmaceutical related field

Jobbeschreibung

## Senior Specialist, Drug SafetyApply: Hybrid: POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center): CRI - San Jose - San Jose (Zurcher): COL - Cundinamarca - Bogotá (Colpatria): Full time: Posted 2 Days Ago: End Date: November 16, 2026 (14 days left to apply): R423310Job Description**The Position**Currently, we are looking for Senior Specialist, Drug Safety. Develop and maintain the necessary processes to ensure high-quality individual case and aggregate safety reporting in accordance with pharmacovigilance (PV) policy and regulations. Maintain knowledge of PV regulations related to drugs, vaccines, biologics and devices. Collaborate with internal and external stakeholders with processes that ensure compliance with local and global PV regulations. **What will you do?*** Lead in the development of processes with internal and external stakeholders to ensure quality and compliance of individual adverse experience case and periodic reports.* Provide expert guidance and perform safety system configuration update and maintenance activities to ensure compliant case data handling as part of the end-to-end Individual Case Safety Report (ICSR) lifecycle: Study Configuration, Product Configuration, Reporting Destinations, Reportability Rules and Label Validation Files.* Support Safety System Development Lifecycle (SDLC) activities to ensure these systems remain compliant with both internal and external requirements and pursue process efficiencies.* Provide content for the ongoing development and expert review of the Global Safety Database User Manual, Standard Operating Procedures, and training material as needed to ensure accuracy.* Provide expert guidance on the PV activities outlined by procedures (SOPs, User Manual, etc.).* Responsible for drafting, negotiation, and maintenance of PV agreements and safety management plans.* Identify and prioritize PV agreements and safety management plans to maintain compliance with worldwide regulatory requirements.* Responsible for the end-to-end GCS&PV implementation and maintenance for select business deals.* Support due diligence and qualification activities for selecting partner deals/projects.* Interact closely with the business system owner for the maintenance of the Business Development Lifecycle Management system.* Perform quality review of expedited and periodic reports to ensure adherence to global case processing standards and regulatory requirements.* Identify, prioritize, and monitor quality issues to be resolved to maintain compliance.* Lead efforts to improve departmental efficiencies and continuous improvement.* Process incoming communications from internal and external sources and initiate appropriate course of action and/or response.* Monitor group mailboxes utilized for the centralization of process/subject specific inquiries.* Assist in preparing and responding to Regulatory Agency Inspections as well as internal and external audits.* Follow company always polices and legal guidelines.* Develop and support processes that facilitate achievement of GCS&PV objectives.* Support any other project or perform any other task deemed appropriate by management.**Qualifications, Skills & Experience Required*** Bachelor's degree or master's degree in life science/health care/pharmaceutical related field.* Candidates are required to have at least two years of pharmacovigilance safety experience or related areas such as Clinical Risk Management, Clinical or Regulatory.* Strong knowledge base of pharmacovigilance principles with close attention to detail and ability to be flexible to meet daily competing priorities of the business.* Demonstrates leadership, and excellent communication and interpersonal skills.* Ability to manage and independently drive projects to completion. **Additional location(s) Compensation Information:****Required Skills:**Adverse Event Report, Auditing, Compliance Monitoring, Data Analysis, Drug Safety Surveillance, Pharmaceutical Regulatory Compliance, Pharmacovigilance, Process Improvements, Quality Compliance, Quality Control Management, Quality Reporting, Regulatory Audits, Regulatory Compliance, Regulatory Inspections, Regulatory Reporting, Regulatory Requirements, Regulatory Reviews, Risk Management, Safety Management**Preferred Skills:**Current Employees apply HERECurrent 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:**Domestic/International**VISA Sponsorship:**No**Travel Requirements:**No Travel Required**Flexible Work Arrangements:**Hybrid**Shift:**Not Indicated**Valid Driving License:**No**Hazardous Material(s):**n/a**Job Posting End Date:**11/16/2026**\\*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.**