Associate Director, Medical Review Lead, MSRM - Remote Agios PharmaceuticalsAssociate Director, Medical Review Lead, MSRM - RemoteAnywhere, NYRemote$185,369–$308,948 / yearThe current base salary range for this position is expected to be between $185,369 and $308,948 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. This role provides oversight of medical review for Individual Case Safety Reports (ICSRs) across investigational and marketed products, ensuring medical accuracy, regulatory compliance, and high-quality safety data to support pharmacovigilance and risk management activities.
Remote | Medical Safety & Drug Safety Expert — $130–$180/hour 24-MagRemote | Medical Safety & Drug Safety Expert — $130–$180/hourNew York, New YorkRemoteSelected experts will work across adverse-event data, patient narratives, DSUR and PBRER reporting, signal interpretation, and structured task development grounded in real-world medical safety practice. We are sharing a specialised part-time consulting opportunity for experienced medical safety and drug safety professionals with substantial expertise in aggregate safety reporting, clinical safety data, benefit-risk assessment, and signal evaluation.
Vice President, Drug Safety and Pharmacovigilance DSPV Immunovant IncVice President, Drug Safety and Pharmacovigilance DSPVNew York, NY$400,000–$425,000 / yearMedical expert accountable for overall DSPV strategy and all deliverables of the DSPV function, including responsibilities for pharmacovigilance-related documents (e.g., DSUR) as well as safety sections of key documents (e.g., IBs, RSI, ICFs, study protocols, CSRs) and other applicable activities (IND/CTA, requests for information, regulatory responses). Responsible for oversight of the DSPV department, including building and managing a team of DSPV professionals (operations and safety science) to execute the development strategy and support registrational/post-marketing activities in a compliant and collaborative environment, in accordance with long-term strategic goals.
Contractor – Senior Drug Safety Specialist Syndax PharmaceuticalsContractor – Senior Drug Safety SpecialistNew YorkRemoteCollaborate with cross-functional teams, Clinical Operations, Data Management and Biostatistics; participate in meetings and teleconferences with cross-functional teams, CROs, and business partners. Generate appropriate queries to sites and/or contract drug safety vendors (CROs) to complete and clarify SAE case information; work with the CRO to determine when cases are complete and ready to close.
Drug Safety Associate Actalent IncDrug Safety AssociatePort Washington, NYRemote$20–$23 / hourIn this role, you"ll play a critical part in supporting the monitoring and reporting of product safety information, helping ensure that patients, healthcare providers, and regulatory authorities receive accurate and timely safety data. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Sr Hazardous Drug Program Spec University of RochesterSr Hazardous Drug Program SpecRochester, New YorkWorker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 100124 Environmental Health & Safety Work Shift: UR - Day (United States of America) Range: UR URG 111 Compensation Range: $64,200.00 - $96,200.00 The referenced pay range represents the minimum and maximum compensation for this job. Ensures the development and implementation of a quality assurance and control program that collects and reports relevant data for adherence to policy and procedures, identification and resolution of quality problems, receipt and evaluation of complaints and potential adverse events reports, and any investigations and corrective action plans as it relates to HazD handling and utilization within the health system.
Senior Director AI and Data Science Drug Discovery and R&D Enablement Lexeo Therapeutics IncSenior Director AI and Data Science Drug Discovery and R&D EnablementNew York, NY$255,000–$302,000 / yearDirector will set direction and deliver applied AI/ML solutions across internal workflows and externally facing outputs, ranging from R&D insights to partner-ready analyses, while partnering closely with scientific teams and, when needed, external vendors/partners to solve real problems. It requires a leader who can build, validate, and operationalize models using real-world biopharma data, raise the signal-to-noise ratio in small or unstructured datasets, and include synthetic control arm approaches where appropriate.
NewBusiness Development Manager - Drug Discovery Eurofins Scientific SEBusiness Development Manager - Drug DiscoveryNew York, NY$115,000–$130,000 / yearEurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialized clinical diagnostics testing. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable.
Remote | Preclinical Drug Discovery & Development Scientist — $50–$90/hour 24-MagRemote | Preclinical Drug Discovery & Development Scientist — $50–$90/hourNew York, New YorkRemoteSelected experts will review scientific materials and development data, evaluate model outputs, contribute practical judgement on drug-development decisions, and help define high-quality data structures grounded in authentic preclinical workflows. This opportunity is best suited to hands-on drug-development professionals rather than backgrounds focused primarily on CRO/CDMO services, academic-only research, QC/analytical functions, clinical development, diagnostics, regulatory affairs, or medical writing.
Senior Director, AI And Data Science (Drug Discovery And R&D Enablement) Lexeo Therapeutics, IncSenior Director, AI And Data Science (Drug Discovery And R&D Enablement)New York, NY$229,500–$332,000 / yearContribute leadership to current and emerging initiatives such as AI workflow automation/database buildouts and analytics agents that leverage enterprise platforms (examples already in motion include CMC AI automation, MaxisAI clinical database/AI efforts, and AI work to ingest historical data into Dataverse/Fabric for agent-based analysis; integration work such as a Benchling AI API initiative may also be in scope depending on priorities). Director will set direction and deliver applied AI/ML solutions across internal workflows and externally facing outputs, ranging from R&D insights to partner-ready analyses, while partnering closely with scientific teams and, when needed, external vendors/partners to solve real problems.
Drug Production, Associate Manufacturing Specialist Regeneron Pharmaceuticals IncDrug Production, Associate Manufacturing SpecialistRENSSELAER, NY$21.78–$39.13 / hourFull cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA). Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs.
Associate Manager, Safety Data and Systems Argenx SEAssociate Manager, Safety Data and SystemsNY$88,000–$121,000 / yearargenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. Note: If the posted hiring range does not apply to your work location, the recruiter will share the locally applicable annual base salary hiring range, provided in your country''s currency, during the recruitment process.
Director, Global Patient Safety Sciences - General Medicine Regeneron PharmaceuticalsDirector, Global Patient Safety Sciences - General MedicineTarrytown, NY$205,000–$341,600 / yearDiscover your role: This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.). Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron's Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs).
Safety Lead Precision Medicine Group LLCSafety LeadNYRemote$110,700–$166,100 / yearPosition Summary: Responsibilities will include but may not be limited to; project specific teleconferences/meetings(i.e. Kick off meetings, internal study specific meetings, client governance meetings) Safety budget review and approval as needed, safety management plan development, oversight of serious adverse event (SAE, SUSARS) case management from intake to regulatory reporting, and providing safety expertise in a timely manner upon request from team members, clients, and study site personnel. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Director, Safety Scientist BeOne Medicines AGDirector, Safety ScientistNY$185,100–$245,100 / yearLead the development, update, and review of safety communication documents (e.g., Dear Investigator Letter, Informed Consent Form, Investigator's Brochure, Healthcare Professional communications (DHCP letter or DHPC), Labelling documents, Risk Management Plan, etc.) in collaboration with Safety Science team members and relevant cross-functional team members. General Description: The Director, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical and scientific expertise to lead the detection of safety signals, evaluation of safety data, assessment of safety risks, responses to regulatory inquiries, and regulatory-required periodic reporting.
Safety, Health & Environmental Manager ManpowerSafety, Health & Environmental ManagerRonkonkoma, NY$50.48–$52.88 / hourManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
Senior Manager, Global Patient Safety - General Medicine Regeneron PharmaceuticalsSenior Manager, Global Patient Safety - General MedicineTarrytown, NY$150,500–$245,500 / yearWe may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron. The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area.
Pharmd Program Associate - Safety Sciences Regeneron PharmaceuticalsPharmd Program Associate - Safety SciencesTarrytown, NY$98,100–$160,100 / yearSafety Sciences - Associate will gain a working knowledge of various pharmacovigilance (PV) disciplines that enable the continuous assessment of the benefit-risk of Regeneron products throughout the product life cycle, from early clinical development through market authorization and including post marketing surveillance, with a focus on signal detection and management. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas.
PharmD Program Associate - Safety Sciences Regeneron Pharmaceuticals IncPharmD Program Associate - Safety Sciencestarrytown, NY$98,100–$160,100 / yearSafety Sciences - Associate will gain a working knowledge of various pharmacovigilance (PV) disciplines that enable the continuous assessment of the benefit-risk of Regeneron products throughout the product life cycle, from early clinical development through market authorization and including post marketing surveillance, with a focus on signal detection and management. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas.
Public Safety Supervisor - Aurora Medical Center Grafton Advocate Health and Hospitals CorporationPublic Safety Supervisor - Aurora Medical Center GraftonPort Washington, Washington$28.55–$42.85 / hourResponsible for KRA results; provides input to and implements the budget, administers policies and procedures, conducts inspections and audits to identify vulnerabilities and hazards; corrects deficiencies identified by third party inspections, audits, and regulatory surveys; meets state and federal compliance regulations (e.g., DNV, Environment of Care chapter of the Joint Commission on Accreditation of Health Care Organizations, CMS, OSHA, etc.). Typically requires 5 years of experience in a security, related public safety, or customer service area that includes experiences in responding to emergent situations and identifying and resolving complex issues that pose a potential risk to patients, visitors, teammatesand/or property.