Senior Scientist, Non Clinical Drug Safety Boehringer Ingelheim International GmbHSenior Scientist, Non Clinical Drug SafetyRidgefield, CT$140,000–$222,000 / yearIndependently performs scientific experiments with a predefined goal including developing new methodologies, protocols and or test procedures that contribute to core group/research goals and reflect expert knowledge; May direct and oversee experimental design and results of technicians and junior level scientists. Develops expertise in a specific project-relevant area or technology; May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects; Ability to work with various LIMS; Compilation of associated outputs with supervision.
Drug Safety Associate III System OneDrug Safety Associate IIIStamford, ConnecticutMinimum 3 years in Drug Safety Operations role; Experience overseeing CRO teams of case processors preferred. Identify adverse events, seriousness, and listedness/labeledness for case assessment; review additional incoming information to determine reportability.
ViiV Healthcare (GSK) Director, Nonclinical Drug Discovery Modeling and Programming GSK plcViiV Healthcare (GSK) Director, Nonclinical Drug Discovery Modeling and ProgrammingBranford, CTThe Director, Nonclinical Drug Discovery Modeling and Programming serves as the scientific and strategic lead for Model-Informed Drug Discovery (MIDD) within ViiV Discovery, driving the application of predictive modeling, simulation, and computational tools to inform portfolio decisions across HIV programs. Leveraging expertise in PBPK, IVIVE, PK/PD, formulation and route-of-administration modeling, the role develops fit-for-purpose modeling approaches and scalable tools that accelerate decision-making from target validation through candidate selection and into early clinical development for multiple modalities (e.g.
Patient Safety Physician, Medical Safety Physician - CRM Boehringer Ingelheim International GmbHPatient Safety Physician, Medical Safety Physician - CRMRidgefield, CT$220,000–$394,000 / yearDepending on the status of development of the compound, may be required to lead, manage and medical-scientifically direct a team of risk management physicians responsible for an investigational compound or product, including project-specific training and coaching of team members, review of team output. Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including: • Chair or support the BI-internal Asset Benefit Risk Team, consisting of experts in Pharmacovigilance, Medical Affairs, Epidemiology and Biostatistics and other disciplines as appropriate.
(Senior) Patient Safety Physician, Medical Safety Physician - Inflammation Boehringer Ingelheim International GmbH(Senior) Patient Safety Physician, Medical Safety Physician - InflammationRidgefield, CT$280,000–$441,000 / yearDepending on the status of development of the compound, may be required to lead, manage and medical-scientifically direct a team of risk management physicians responsible for an investigational compound or product, including project-specific training and coaching of team members, review of team output. • Plan, manage / perform and monitor all pharmacovigilance activities for assigned drug responsibilities, including: • Chair or support the BI-internal Asset Benefit Risk Team, consisting of experts in Pharmacovigilance, Medical Affairs, Epidemiology and Biostatistics and other disciplines as appropriate.
Drug Metabolism and Pharmacokinetics - Laboratory Operations Specialist II Boehringer Ingelheim International GmbHDrug Metabolism and Pharmacokinetics - Laboratory Operations Specialist IIRidgefield, CT$75,000–$122,000 / yearFunctions effectively as a team member, demonstrating the behaviors and attributes required to complete interdependent and cross-functional tasks in a highly dynamic work environment. The Bioanalysis-DMPK Laboratory Operations Specialist II supports operational and logistical functions serving the various Bioanalysis-DMPK laboratories with minimal supervision.
Scientist IV, Drug Metabolism and Pharmacokinetics Boehringer IngelheimScientist IV, Drug Metabolism and PharmacokineticsRidgefield, CT$115,000–$181,000 / yearExperimental Medicine, BDS, CBOs, Clinical Operations, NCS Study Directors, and DMPK leads) for protocol development and review, sample handing, sample analysis plans, data transfers, milestones, report timelines, accurate budgeting, and other clinical/nonclinical requirements. Additionally, this role is responsible for the scientific monitoring and outsourcing of clinical and nonclinical bioanalytical studies, serving as the primary key contact and liason between DMPK, clinical trial teams, Nonclinical Safety, and bioanalytical CROs.
Senior Scientist, Computational Safety Boehringer Ingelheim International GmbHSenior Scientist, Computational SafetyRidgefield, CT$140,000–$222,000 / yearThe Senior Scientist will play a key role in curating and consolidating diverse tox and biological data (e.g., omics, genetics, literature, RWD, competitive intelligence) for agentic AI model development for next generation target liability assessment and prediction toxicology efforts. Collaborate closely and effectively communicate with Toxicology, Discovery, Bioinformatics, Data Science, and IT teams to ensure alignment of computational approaches with biological context, technical infrastructure, and project needs.
Lead Patient Safety Physician - CRM Boehringer Ingelheim International GmbHLead Patient Safety Physician - CRMRidgefield, CT$280,000–$441,000 / yearDepending on the status of development of the compound, may be required to strategically lead, manage and medical-scientifically direct a team of risk management physicians responsible for an investigational compound, product or portfolio compound/product or project including project management, project-specific training and coaching of team members, review of team output. This role is accountable for proactive risk management of assigned key marketed and/or investigational compound or a product family including continuous assessment of the benefit-risk profile and performing risk minimization as required to ensure safe use in patients.
Principal Scientist, Process Safety Boehringer Ingelheim International GmbHPrincipal Scientist, Process SafetyRidgefield, CT$140,000–$222,000 / yearDirects a team of multiple disciplinary personnel to perform experiments to define process parameters intended for manufacturing API for later stage clinical trials and even for commercialization; Must apply organic chemistry, chemical engineering, safety and green chemistry principles to design experiments, optimize reactions, streamline workup procedures, and reduce cycle times. Manages all aspects of laboratory and scale up operations including recruiting, coaching, mentoring, training, supervising and developing junior scientific staff and ensuring that entire staff is trained and working in conformance with cGMP requirements, BIPI policies, SOPs and safety regulations.
NewGlobal Pharmacovigilance (PV) Senior Scientist Amgen IncGlobal Pharmacovigilance (PV) Senior ScientistBridgeport, CTIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.
Pharmacovigilance Triage Manager II (Hybrid) Boehringer Ingelheim International GmbHPharmacovigilance Triage Manager II (Hybrid)Ridgefield, CT$140,000–$222,000 / yearThrough collaboration with Risk Management (RM) Physicians, Study Coordination, Regulatory Affairs, Biostatistics and Data Science (BDS) and Clinical Operations, this position ensures that adverse event information regarding the company´s products is submitted to the appropriate business units and health authorities. In addition to understanding all company policies, procedures, guidelines and working instructions regarding the reporting of adverse events, must be familiar with clinical trial protocols, product labels, company core data sheets, investigator brochures, medical terminology dictionaries and federal regulations.
Pharmacovigilance Triage Manager II Boehringer Ingelheim International GmbHPharmacovigilance Triage Manager IIRidgefield, CT$140,000–$222,000 / yearThrough collaboration with Risk Management (RM) Physicians, Study Coordination, Regulatory Affairs, Biostatistics and Data Science (BDS) and Clinical Operations, this position ensures that adverse event information regarding the company´s products is submitted to the appropriate business units and health authorities. In addition to understanding all company policies, procedures, guidelines and working instructions regarding the reporting of adverse events, must be familiar with clinical trial protocols, product labels, company core data sheets, investigator brochures, medical terminology dictionaries and federal regulations.
SR AD / Director, Clinical Development Operations Lead (CDOL/SR CDOL), Obesity/MASH - Remote Boehringer IngelheimSR AD / Director, Clinical Development Operations Lead (CDOL/SR CDOL), Obesity/MASH - RemoteRidgefield, CTRemote$170,000–$269,000 / yearIt works in close collaboration with Clinical Operations, Statistics, Regulatory Affairs, Drug Safety, and other key functions to design robust operational strategies, establish data-driven timelines, and ensure high-quality trial execution across programs. The Clinical Development & Operations Lead (CDOL) is member of Clinical Development Organization responsible for defining and delivering operational strategy for late-phase clinical programs within assigned indications or assets, with a strong focus on speed, quality, and value.