Remote Pharmacovigilance / Drug Safety Pharmacist Pharmacy CareersRemote Pharmacovigilance / Drug Safety PharmacistAlabamaRemoteRemote Pharmacovigilance Pharmacist – Drug Safety From Home | No Prior Pharma Experience Required Contribute to global patient safety by collecting, evaluating, and documenting adverse events — entirely from home. This role is open to pharmacists from hospital, ambulatory, community, or managed care backgrounds who have strong attention to detail and want to enter the pharmaceutical industry.
Director, Drug Safety & Pharmacovigilance Operations Rigel Pharmaceuticals IncDirector, Drug Safety & Pharmacovigilance OperationsSouth San Francisco, CA$210,000–$250,000 / yearProvide operational leadership and ensure cross-functional delivery of aggregate and summary safety reports, including IND Annual Reports, DSURs, PSURs/PBRERs, PADERs, integrated safety summaries, and related safety sections of protocols, CSRs, and regulatory submissions. Serve as business owner or senior operational lead for the safety database and related systems; define the roadmap and govern access, configuration changes, controlled terminology, data outputs, upgrades, validation/UAT, and vendor-hosted environments, as applicable.
Director, Drug Safety & Pharmacovigilance Scientist Dyne Therapeutics IncDirector, Drug Safety & Pharmacovigilance ScientistWaltham, MA$220,000–$240,000 / yearRole Summary: The Director, Drug Safety & Pharmacovigilance Scientist provides strategic and scientific leadership for safety surveillance, signal detection, benefit-risk evaluation, and risk management activities across Dyne's development programs. The Director collaborates across Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, Biostatistics, Data Management, Quality, and external partners to support proactive safety oversight and informed program decision-making.
Senior Medical Director, Global Drug Safety ReplimuneSenior Medical Director, Global Drug SafetyWoburn, Massachusetts$307,000–$397,000 / yearThis position provides pharmacovigilance expertise to and lead collaborations with external partners as well as with other functions across Replimune, including Regulatory Affairs, Clinical Development, Clinical Operations, Medical Affairs, or the Commercial to ensure that drug safety communications are accurate, complete and consistent. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
NewManager, Global Drug Safety & Pharmacovigilance Asahi Kasei Advance AmericaManager, Global Drug Safety & PharmacovigilanceCary, North Carolina$120,000–$130,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This position is primarily responsible for providing management level oversight, planning and execution of post-marketing and clinical trial safety activities ensuring compliance, quality, inspection readiness and operational excellence.
NewManager, Global Drug Safety & Pharmacovigilance Bionique ScientificManager, Global Drug Safety & PharmacovigilanceCary, North Carolina$120,000–$130,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This position is primarily responsible for providing management level oversight, planning and execution of post-marketing and clinical trial safety activities ensuring compliance, quality, inspection readiness and operational excellence.
Senior Director of Drug Safety XtalPi IncSenior Director of Drug SafetySan Diego, CAWorking at the interface of computational design, translational biology and preclinical development, you will integrate mechanistic toxicology, pharmacology, DMPK and emerging clinical insights to enable informed, data-driven programme decisions and successful human translation. Reporting to the VP, Head of In Vivo Bioscience, the role will shape nonclinical and translational safety strategies supporting the progression of novel biologics, multi-specific antibodies and peptide therapeutics from discovery through early clinical development.
Drug Safety Associate I Corbus Pharmaceuticals Holdings IncDrug Safety Associate IThe Drug Safety Associate I will serve as the primary ICSR case processor, managing end-to-end intake and data entry in Veeva Vault Safety and ensuring expedited regulatory submissions meet ICH E2B and FDA/EMA timelines. Corbus' lead oncology program, CRB-701, is a next-generation antibody-drug conjugate (ADC) targeting Nectin-4-expressing tumors and is being developed for multiple solid tumor indications.
VP of Drug Safety/Pharmacovigilance Compass TherapeuticsVP of Drug Safety/PharmacovigilanceBoston, MassachusettsProvide executive oversight and review of safety-related regulatory submissions, cross functionally collaborating with Clinical, Medical, Quality, and Regulatory, including DSURs, DCSI, Risk Management Plans, Investigator Brochures, Clinical Study Report, Informed Consent Forms (ICFs), protocols, reports, other required safety documentation in accordance with legal requirements, respective SOPs and Health Authority. Ensure patient safety by monitoring patient safety profiles to identify and mitigate potential risks associated with Compass drugs; recommend updates to Development Core Safety Information (DCSI)/Reference Safety Information, communicate risks to applicable stakeholders.
Manager/Sr. Manager, Drug Safety & PV Insmed, Inc.Manager/Sr. Manager, Drug Safety & PVJapan, MOAbout the Role: This role is mainly responsible for participating in the Drug Safety and Pharmacovigilance activities including operational works on Pharmacovigilance (PV) and Post-Marketing Study (PMS); training related to PV and PMS activities; quality control and assessment on PV and PMS activities; record management on PV and PMS activities; vendors/temporary staff management, and supporting for communication with regulatory authorities. What You'll Do: Participate in ICSR case management, as well as the maintenance of safety database and establishment of the processes of handling case reports with safety database, lead the process for local aggregate safety reports including J-DSUR and ensure all regulatory safety documents are processed and submitted according to regulatory requirements and timelines.
NewManager, Global Drug Safety & Pharmacovigilance Asahi Kasei Plastics North America, Inc.Manager, Global Drug Safety & PharmacovigilanceCary, North Carolina$120,000–$130,000Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. This position is primarily responsible for providing management level oversight, planning and execution of post-marketing and clinical trial safety activities ensuring compliance, quality, inspection readiness and operational excellence.
Senior Manager, Drug Safety and Medical Monitoring Supernus PharmaceuticalsSenior Manager, Drug Safety and Medical MonitoringRockville, MarylandConduct medical reviews of Individual Case Safety Reports (ICSRs), including Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs), Adverse Drug Reactions (ADRs), causality assessments, signal detection, case narratives, aggregate reports, and safety data listings, and communicate all applicable comments to the Pharmacovigilance Lead. Conduct medical reviews of clinical trial documents including clinical trial protocols, informed consent forms, Investigator’s Brochure and other essential study documents and plans, and provide input to Clinical Development, Medical Writing, and Clinical Operations teams.
Drug Safety Physician SystImmune, Inc.Drug Safety PhysicianPrinceton, NJ$150,000–$250,000 / yearThis individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Drug Safety Physician Systimmune IncDrug Safety PhysicianPrinceton, NJ$150,000–$250,000 / yearThis individual will also support the clinical R&D team in the oversight of PV service vendors and partners and will need to maintain medical knowledge, as well as current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Vice President, Nonclinical Drug Safety & Toxicology Remix TherapeuticsVice President, Nonclinical Drug Safety & ToxicologyWatertown, MA$293,000–$358,000 / yearThe Non-Clinical Safety and Toxicology leader will partner cross-functionally across therapeutic areas with colleagues in drug discovery, translational, and clinical development functions, ensuring toxicology and nonclinical safety data is shared and communicated transparently and plays a role in informing strategy at all stages of each program’s development. Reporting to the Chief Scientific Officer, the Vice President of Nonclinical Drug Safety and Toxicology is a key position within the R&D leadership team and will lead nonclinical aspects of all the company’s pipeline programs.
Senior Medical Director, Global Drug Safety Replimune Group, Inc.Senior Medical Director, Global Drug SafetyWoburn, MA$307,000–$397,000 / yearThis position provides pharmacovigilance expertise to and lead collaborations with external partners as well as with other functions across Replimune, including Regulatory Affairs, Clinical Development, Clinical Operations, Medical Affairs, or the Commercial to ensure that drug safety communications are accurate, complete and consistent. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Medical Director, Global Drug Safety ReplimuneMedical Director, Global Drug SafetyWoburn, Massachusetts$257,500–$333,500 / yearThe RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.
US_Drug Safety Consultant II TalentBurst, Inc.US_Drug Safety Consultant IICambridge, MA$79.61 / hourPosition Summary The PV Aggregate Reports Scientist is part of the Safety Surveillance and Aggregate (SSA) Reports team and is responsible for managing the processes for all aggregate reports (PSURs, DSURs, PADERs, and local reports). Schedule & Regulatory Oversight: Support the Aggregate Reports Master Schedule (production, updates, stakeholder reviews), conduct worldwide legislation reviews for aggregate reporting, and provide impact assessments.
Senior Specialist, Drug Safety CRISPR TherapeuticsSenior Specialist, Drug SafetySouth Boston, MassachusettsThe Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. The Company continues to expand its leadership in gene editing through the development of SyNTase editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction.
Product Solution Manager - Drug Testing & Occ Health & Safety (Hybrid) Quest Diagnostics IncProduct Solution Manager - Drug Testing & Occ Health & Safety (Hybrid)Lenexa, KSQualifications: Required Work Experience: 3-5 years of experience in the workplace drug screening and occupational health industryStrong background in Product Management / Product Operations, with a proven track record of managing complex product implementations, lifecycle optimization, and cross-functional operational alignmentDemonstrated ability to apply strategic frameworks to everyday product operations, turning high-level business goals into rigorous, measurable operational realities. Skills: Advanced process mapping skills to streamline complex operational handoffs between labs, clinics, and digital platforms Proven ability to translate strategic product visions into scalable, repeatable go-to-market operational playbooksData-driven approach to establishing and monitoring operational metrics like turnaround time, cost-to-serve, and implementation velocity.