Senior PV Clinical Scientist - Hybrid Genesis10Senior PV Clinical Scientist - HybridSouth San Francisco, CATemporaryContractorFull timeAptask Global Workforce (AGW) is seeking a Senior PV Clinical Scientist - Hybrid for a 6+ month contract opportunity with a Global Biotechnology Company located in South San Francisco, CA. This role performs tactical and operational responsibilities for the US Patient Safety team, including the collection, clinical review, evaluation, and processing of adverse event (AE) information.
Principal Scientist (Scientific Director Level)- Nonclinical Drug Safety Merck & Co IncPrincipal Scientist (Scientific Director Level)- Nonclinical Drug SafetySouth San Francisco, CA$176,200–$277,300 / yearThey are responsible for 1) providing risk assessments for targets, 2) de-risking strategies for discovery programs and 3) collaborating with NDS staff at other sites to execute on the appropriate studies to support selection of therapeutic targets, and the identification and development of new drug candidates. The Discovery Program Leader is responsible for defining and overseeing the NDS strategy for programs in all modalities (including small molecules, peptides, biologics and ADC programs) from Target Identification through to the approval of First-In-Human enabling GLP toxicity studies.
Medical Director, Drug Safety and Pharmacovigilance Ideaya Biosciences IncMedical Director, Drug Safety and PharmacovigilanceSouth San Francisco, CA$268,000–$331,000 / yearThe final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates' experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process. Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term incentive plan participation, and company discretionary stock option awards (based on board approval).
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.
Lead Drug Safety Physician Thorough GroupLead Drug Safety PhysicianRedwood City, CaliforniaWorking closely with senior leadership and cross-functional partners, this individual will help shape the safety strategy for both investigational and marketed therapies while supporting multiple mid- and late-stage clinical development programs. Thorough Group is partnering with an established, growing biopharmaceutical company to identify an experienced Lead Drug Safety Physician to provide medical leadership across its expanding clinical and commercial portfolio.
Senior Vice President, Drug Safety And Pharmacovigilance Mirum Pharmaceuticals IncSenior Vice President, Drug Safety And PharmacovigilanceFoster City, CAThe SVP leads the department and also works collaboratively across a team of peers in Clinical, Regulatory, Biometrics, Medical Affairs and Commercial and will be accountable for ensuring safety systems, staff and procedures are in place to support a compliant global pharmacovigilance system. Proven professional track record of strategic, organizational, and executional skills to support project planning across multiple activities, with the ability to anticipate and prioritize team workload on multiple ongoing projects.
Senior Vice President, Drug Safety and Pharmacovigilance Mirum Pharmaceuticals IncSenior Vice President, Drug Safety and PharmacovigilanceFoster City, CAThe SVP leads the department and also works collaboratively across a team of peers in Clinical, Regulatory, Biometrics, Medical Affairs and Commercial and will be accountable for ensuring safety systems, staff and procedures are in place to support a compliant global pharmacovigilance system. Proven professional track record of strategic, organizational, and executional skills to support project planning across multiple activities, with the ability to anticipate and prioritize team workload on multiple ongoing projects.
NewDirector, Drug Safety Nurix Therapeutics, Inc.Director, Drug SafetyBrisbane, CA$247,300–$280,400 / yearAs Director, Drug Safety, you'll lead aggregate safety analysis, benefit-risk assessments, and safety strategy for assigned programs - shaping how we evaluate risk and bring new medicines safely to patients. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Associate Director, Drug Safety Physician Rigel Pharmaceuticals IncAssociate Director, Drug Safety PhysicianSouth San Francisco, CA$210,000–$250,000 / yearLead evaluation of complex drug safety data to identify safety signals and evaluate signals for evidence of causal association with precision oncology products, applying advanced analytical techniques and clinical judgment. POSITION SUMMARY: The Drug Safety Physician in Drug Safety & Pharmacovigilance department will serve as a subject matter expert and thought leader for drug safety activities across Rigels portfolio.
NewDirector, Drug Safety Nurix Therapeutics IncDirector, Drug SafetyBrisbane, CA$247,300–$280,400 / yearAs Director, Drug Safety, you'll lead aggregate safety analysis, benefit-risk assessments, and safety strategy for assigned programs - shaping how we evaluate risk and bring new medicines safely to patients. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Senior Specialist I, Patient Safety & Pharmacovigilance (Clinical Trial Safety Operations) Corcept TherapeuticsSenior Specialist I, Patient Safety & Pharmacovigilance (Clinical Trial Safety Operations)Redwood City, CA$103,600–$137,100 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. This role supports Patient Safety and Pharmacovigilance (PSPV) Safety Operations by ensuring the quality, compliance, and timely reporting of safety information from company-sponsored clinical trials, Investigator-Initiated Studies, and expanded access/compassionate use programs.
Senior Specialist I, Patient Safety & Pharmacovigilance Clinical Trial Safety Operations Corcept Therapeutics IncSenior Specialist I, Patient Safety & Pharmacovigilance Clinical Trial Safety OperationsRedwood City, CA$103,600–$137,100 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. This role supports Patient Safety and Pharmacovigilance (PSPV) Safety Operations by ensuring the quality, compliance, and timely reporting of safety information from company-sponsored clinical trials, Investigator-Initiated Studies, and expanded access/compassionate use programs.
NewCo-founder & CTO, AI for predictable drug discovery and development Deep Science VenturesCo-founder & CTO, AI for predictable drug discovery and developmentSan Francisco, CAThe causes run from efficacy to safety to commercial choice, and the claim here is narrower than blaming that number on translation: the field still lacks a systematic way to measure how far a given experimental result should carry into a specific therapeutic decision. Hierarchical and Bayesian inference, classical statistics, graph learning including graph neural networks, probabilistic graphical models and learned calibration.
Clinical Psychologist (Drug Abuse Program Coordinator) U.S. Department of JusticeClinical Psychologist (Drug Abuse Program Coordinator)San Francisco, CA$105,481–$137,128 / yearIf you are on active duty and expect to be discharged or released from active duty service within 120 days, you may submit a Certificate of Release or Discharge from Active Duty from the appropriate Branch Personnel Office containing the following information: The military service dates including the expected discharge or release date; and. The incumbent has professional autonomy in directing and supervising all clinical activities and staff in relation to the drug treatment of Bureau inmates, including: testing, test interpretation, clinical diagnosis, clinical staffing of inmates with staff and serving as the institution advocate for drug programs with all staff, including Executive staff.
Associate Director, Drug Substance Manufacturing - Upstream Process Vera Therapeutics IncAssociate Director, Drug Substance Manufacturing - Upstream ProcessBrisbane, CA$175,000–$210,000 / yearWorking with the CMC team and other key functions such as project management, QA and Regulatory, the ideal candidate must be an outstanding leader with a proven track record of overseeing all drug-substance upstream manufacturing activities at the CMO site, including process scale-up, technology transfers, validations, PPQ campaign support, continuous process improvements, and post-approval lifecycle management of commercially approved products. The individual will serve as a subject matter expert (SME) in upstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global regulatory submissions of complex Biologics, monoclonal antibodies, and other recombinant therapeutics.
Associate Director, Medical Safety Science (Safety Scientist) Mirum Pharmaceuticals IncAssociate Director, Medical Safety Science (Safety Scientist)Foster City, CA$215,000–$230,000 / yearThe ideal candidate will have experience in and perform multiple activities related to safety data review, document review, signal detection and management, authoring of aggregate reports and participating in multidisciplinary meetings. Minimum 7 years in pharmaceutical or CRO experience in clinical trial or post-market setting, 5 years in a drug safety and pharmacovigilance role (specifically, as a Safety Scientist).
Associate Director, Medical Safety Science Safety Scientist Mirum Pharmaceuticals IncAssociate Director, Medical Safety Science Safety ScientistFoster City, CA$215,000–$230,000 / yearThe ideal candidate will have experience in and perform multiple activities related to safety data review, document review, signal detection and management, authoring of aggregate reports and participating in multidisciplinary meetings. Minimum 7 years in pharmaceutical or CRO experience in clinical trial or post-market setting, 5 years in a drug safety and pharmacovigilance role (specifically, as a Safety Scientist).
NewSenior Drug Discovery Scientist AxiomSenior Drug Discovery ScientistSan Francisco, CaliforniaPartner directly with drug hunters at top pharma companies, researchers at leading AI labs, and Axiom’s multidisciplinary team to build the experimental datasets and agentic systems needed to accurately predict human outcomes, then deploy those systems into real discovery workflows to inform major go/no-go decisions across high-value drug programs. In this role, they will work directly with great scientists at top pharma and biotech companies, researchers from leading AI labs, and Axiom’s multidisciplinary team to build the experimental datasets, agentic systems, and product capabilities needed to accurately predict human drug outcomes.
FSP - Scientist - Formulations, Drug Delivery Thermo Fisher ScientificFSP - Scientist - Formulations, Drug DeliverySouth San Francisco, CaliforniaWith clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Analytical Characterization: Independently analyze formulations using a diverse suite of analytical techniques (including spectroscopy, rheology, chromatography, calorimetry, light scattering, and physicochemical property measurements) to assess structure, composition, and physicochemical properties.
Scientist I OR Scientist II, DevOps Drug Substance, ONSITE, Fremont CA Boehringer Ingelheim International GmbHScientist I OR Scientist II, DevOps Drug Substance, ONSITE, Fremont CAFremont, CA$60,000–$122,000 / yearOperating as a DevOps DS project team member and occasionally as a team leader/coordinator, the incumbent applies scientific principles and process knowledge and expertise in cell culture and/or purification CMC development to execute, analyze, and document complex experiments with regular team interaction, and develop solutions to address frequently encountered problems. Operating as a DevOps DS project team member and occasionally as a coordinator, the incumbent applies scientific principles and process knowledge and expertise in cell culture and/or purification CMC development to execute, analyze, and document routine experiments with minimal oversight and complex experiments with regular team interaction.