Sr. Scientist, Drug Safety

Job DescriptionThe Senior Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. The CSS will collaborate with cross-functional colleagues within clinical development, clinical operations, case processing and medical safety review.Key ResponsibilitiesIntake of reportable safety event information from clinical trial investigator sites.Review and manage individual case safety reports for each event.Ensure that all information required for a clinically complete and accurate case is present.Generate safety queries to the trial investigator sites to ensure case report accuracy and completeness.Prioritize daily work to ensure all events are submitted for entry into the safety database within the established timeframes.Complete protocol specific activities as requiredActively participate and ensure effective communication with other team members supporting their protocolsAppropriately escalate protocol or individual event issues with other stakeholders including CRAs/CRMsPerform protocol lead activities for a trial.Triage safety queries from the clinical team and medical safety review teamParticipate as a core member of the Medical Monitoring TeamParticipate as an extended member of the Clinical Trial TeamReconcile critical data points between clinical and safety databaseCollaborate closely with cross functional colleagues May collaborate with external colleagues and business partners. May serve as an expert resource for less experienced colleagues.May provide training /coaching for new employees. May participate in cross-functional or internal initiatives and/or process improvement projects.May provide support to outsourced trialsMay serve as a Business Support team Leader.Required SkillsAccountability, Accountability, Adaptability, Adverse Event Report, Clinical Development, Clinical Experience, Clinical Medicine, Clinical Physiology, Clinical Reporting, Clinical Trials, Clinical Trials Monitoring, Data Analysis, Data Integrity, Decision Making, Drug Safety Surveillance, Good Clinical Practice (GCP), Innovation, Machine Learning (ML), Medical Review, Medical Writing, Pharmacovigilance, Process Improvement Projects, Product Development, Regulatory Compliance, Risk Management {+ 3 more}Preferred SkillsCurrent Employees apply HERECurrent Contingent Workers apply HERESearch 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 VISA Sponsorship Travel RequirementsFlexible Work Arrangements HybridShift Valid Driving License Hazardous Material(s) Job Posting End Date 11/23/2025A 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 R375309