NewSenior Director, Clinical Portfolio and Program Management Allogene TherapeuticsSenior Director, Clinical Portfolio and Program ManagementSouth San Francisco, CARemote$230,000–$270,000 / yearWork with the program team members to facilitate project/program execution from Pre-IND planning through BLA/MAA approvals utilizing project management tools and processes to maintain strategic direction, project schedule/timeline, communications, budget/cost and identify and mitigate risks. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
Senior Director, Clinical Portfolio and Program Management Allogene Therapeutics IncSenior Director, Clinical Portfolio and Program ManagementSouth San Francisco, CA$230,000–$270,000 / yearWork with the program team members to facilitate project/program execution from Pre-IND planning through BLA/MAA approvals utilizing project management tools and processes to maintain strategic direction, project schedule/timeline, communications, budget/cost and identify and mitigate risks. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914 Ascendis PharmaAssociate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914Palo Alto, CA$255,000–$265,000Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed.
NewAssociate Clinical SAS Programmer/Junior Statistician Heartflow IncAssociate Clinical SAS Programmer/Junior StatisticianSan Francisco, CARemote$86,000–$112,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and generating the outputs required for, conference, publication, and regulatory submissions.
Director of Quality Assurance, Clinical Caribou Biosciences, Inc.Director of Quality Assurance, ClinicalBerkeley, CA$220,000–$235,000 / yearProvide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline. The successful candidate must have the ability to execute QA tasks independently; effectively represent QA in a GCP, PV, and GLP focused team settings and manage quality related activities related to clinical vendors, investigator sites and regulatory agencies.
Clinical Trials Manager (Biotechnology, Oncology) Exelixis IncClinical Trials Manager (Biotechnology, Oncology)Alameda, CA$136,000–$192,500 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BA/BA/BSN in biological sciences or related field and a minimum of 7 years of related experience; or, MS/MA/MSN in biological sciences or related field and a minimum of 5 years of related experience; or, PhD/PharmD in biological sciences or related field and zero or more years of related experience; or, Equivalent combination of education and experience. This position is responsible for overseeing the execution of clinical trials, collaborating with cross-functional teams, performing oversight activities of Contract Research Organizations (CROs), and providing operational support to the Study Delivery Lead (SDL).
Provider Clinical Operations Consultant, Senior Associate PricewaterhouseCoopers LLPProvider Clinical Operations Consultant, Senior AssociateSan Francisco, CA$77,000–$202,000 / yearPreference for at least one of the following fields of study: Accounting, Actuarial Science, Analytics/Data Science, Business Administration/Management, Computer Science/Information Systems, Economics, Engineering, Finance, Government/Public Policy, Health Administration/Public Health, Mathematics/Statistics, Operations/Supply Chain, Organizational Management/Behavior, Risk Management/Insurance. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Manager of Research Clinic Kaiser PermanenteManager of Research ClinicOakland, CACoordinates and manages clinical research by: guiding and coordinating team in the preparation and submission of a portfolio of research proposals as applicable; guiding and coordinating team in the collection, management, analyses, and interpretation of clinical trials data; orchestrating internal resources needed to provide consultation on implementing clinical trials for staff; influencing the development and implementation of policies and procedures for developing research protocols and other processes of clinical trials; overseeing the preparation, submission, and/or compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for training others to execute clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in training others to support research lab operations(e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). Guides research compliance by: leveraging advanced knowledge of clinical trials while planning the effective, long-term design of clinical trial applications to ensure compliance with all applicable federal, state, and local regulations and KP policies and procedures within unit or team; developing guidance for identifying and resolving compliance and/or quality issues and developing corrective action plans; developing and socializing updates for compliance-monitoring/audit systems and documentation; leading the implementation of new or updated research protocols, procedures, and guidance to ensure confidentiality, privacy, and security of clinical research data; driving the implementation of research protocols, procedures and guidance to ensure confidentiality, privacy, and security of clinical research data within unit; and overseeing and advising team members who are providing guidance and partnering with investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines.
Senior Research Scientist MastarRecSenior Research ScientistSan Francisco, CaliforniaMastarRec is recruiting a Senior Research Scientist to support biotechnology and life sciences organizations across the United States to join our cutting-edge research team driving innovation in genomics, transcriptomics, and multi-omics data analysis. In this role, you will lead the development of scalable computational methods, analyze next-generation sequencing (NGS) datasets, and collaborate with interdisciplinary teams across biotechnology, clinical research, and personalized medicine.
Sr. Clinical Trial Manager Structure Therapeutics IncSr. Clinical Trial ManagerSouth San Francisco, CA$171,000–$223,000 / yearIdentifies potential study issues/risks, escalates as needed and recommends/implements Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up. Minimum of 7+ years of related industry experience as a Clinical Research Associate or related function with increasing responsibility and scope Minimum of 3+ years study management experience in clinical and drug development Experience in selecting, managing, and overseeing sites, CROs, specialty labs and other service providers in global, multinational studies or programs.
Sr. Clinical Trial Manager (Mp) Structure Therapeutics IncSr. Clinical Trial Manager (Mp)South San Francisco, CA$171,000–$218,000 / yearIn collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements). Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
Sr. Clinical Trial Associate ALX Oncology Inc.Sr. Clinical Trial AssociateSouth San Francisco, CA$115,000–$125,000 / yearCTA) supports clinical trial execution from study start-up through close-out, with increasing ownership of activities including Trial Master File (TMF) management, site activation, study tracking, vendor coordination, and study documentation. Support oversight of CROs and other study vendors, including tracking deliverables, timelines, documentation, system access and assisting with review of vendor and study plans; proactively identify and address routine issues and escalate risks as appropriate.
Clinical Assistant/Associate Professor Medical Physics Position at Stanford - Oakland Regional Center (Lead) Stanford UniversityClinical Assistant/Associate Professor Medical Physics Position at Stanford - Oakland Regional Center (Lead)Oakland, CA$194,000–$387,000 / yearThe department operates a wide range of state-of-the-art equipment, including two Accuray CyberKnife systems, one RefleXion X1, one ViewRay MRIdian, one Mevion S250Fit proton therapy platform, and three Varian TrueBeams at Palo Alto campus. The pay offered to the selected candidates will be determined based on factors including (but not limited to) the experience and qualifications of the selected candidates including equivalent years in rank, training, and field or discipline; internal equity; and external market pay for comparable jobs.
AI/ML Research Engineer Manifold Bio IncAI/ML Research EngineerSan Francisco, CAYou will be expected to take ownership of engineering challenges in our ML pipeline, from data processing and model training to deployment and monitoring, while collaborating closely with our research team to translate cutting-edge ideas into robust, scalable systems. Our in vivo-centric discovery platform produces millions of experimentally validated protein designs per campaign, creating the datasets that make our models possible and our approach uniquely powerful.
Sr. Research Associate/Associate Scientist, Protein Biochemistry AllakosSr. Research Associate/Associate Scientist, Protein BiochemistryRedwood City, CaliforniaSenior Research Associate/Associate Scientist, Protein Biochemistry Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammatory and proliferative diseases. Position Summary: We are seeking a highly motivated Senior Research Associate/Associate Scientist with a strong background in protein biochemistry to join our R&D team.
Clinical project Associate Integrated Resources, IncClinical project AssociateFoster City, CaliforniaContractorDistributes updated study related documents (i.e. Investigative Brochures, package inserts) to study teams and internal departments as requested by the CTMA or CTM.Under close supervision reviews and participates in the quality assurance of data or documents including and not limited to GILDA and DataVision. Job DescriptionTitle: Clinical Project AssociateDuration: 06 MonthsLocation: Foster City, CAJob Responsibilities & SkillsProject involvement will be in an administrative role.
Scientist II, Translational Research Tempus AI IncScientist II, Translational ResearchRedwood City, CA$90,000–$135,000 / yearDemonstrated ability to influence without authority (both with internal and external stakeholders Proactive mindset that bridges ideas to implementable solutions, and can help move both internal and external stakeholders to quickly solve problems Experience with communicating insights and presenting concepts to diverse audiences. Work with Product and Engineering teams to streamline workflow of computational analyze Contribute to the development of the portfolio by providing feedback to leadership regarding client responses and suggestions; maintain a solution-oriented mindset.
Staff II Pharmacist - Hematology/Oncology Clinical Pharmacist UCSF Medical CenterStaff II Pharmacist - Hematology/Oncology Clinical PharmacistSan Francisco, CAThese include, for example, obtaining medication histories, reviewing and assessing medication profiles, providing drug information to patients and health care providers, collaborating with clinicians on drugs of choice and therapeutic plans, ensuring access to medications, educating patients on the proper use of medications, and ensuring that patients understand cautions, adverse reactions, and interactions related to their therapy. These services include, but are not limited to: drug procurement, storage, and security; safe, accurate and timely preparation and distribution of drugs; clinical pharmacy services for patients; development of drug use policies within the Medical Center; drug information services for clinicians and patients; and participation in technology assessment and quality assurance programs.
Abdominal Transplant Clinical Pharmacist UCSF Medical CenterAbdominal Transplant Clinical PharmacistSan Francisco, CAThese include, for example, obtaining medication histories, reviewing and assessing medication profiles, providing drug information to patients and health care providers, collaborating with clinicians on drugs of choice and therapeutic plans, ensuring access to medications, educating patients on the proper use of medications, and ensuring that patients understand cautions, adverse reactions, and interactions related to their therapy. These services include, but are not limited to: drug procurement, storage, and security; safe, accurate and timely preparation and distribution of drugs; clinical pharmacy services for patients; development of drug use policies within the Medical Center; drug information services for clinicians and patients; and participation in technology assessment and quality assurance programs.
Senior Research Associate/Associate Scientist AllakosSenior Research Associate/Associate ScientistRedwood City, CaliforniaSenior Research Associate/Associate Scientist Allakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammatory and proliferative diseases. Your Role: Design and execute in vitro/ex vivo cell and flow cytometry-based assays with primary cells from human and mouse tissues.