UNKNOWN

FEED

You will help us secure both our AWS infrastructure and our code base, partnering directly with engineering and other security teams to identify risk, improve architecture, investigate incidents, and build practical security controls. Outset is backed by top Silicon Valley investors and raised a $30M Series B in December 2025—less than six months after our Series A—led by Radical Ventures with participation from M12 (Microsoft’s venture arm), 8VC, Y Combinator, and Adverb Ventures.

Outset

Platform Security Engineer

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How should global clinical execution be designed and operationally managed for rare kidney diseases and genetically defined patient populations, including oversight of CROs, sites, and regional partners?. Which investigator networks, patient advocacy organizations, and clinical sites will be most critical to successful development, and how should those relationships be cultivated, coordinated, and leveraged throughout the clinical lifecycle?.

YEAR

5AM Ventures

Director/Senior Director, Clinical Operations

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With a highly experienced team of experts in immunology and drug development, we are pioneering innovative approaches to target and modulate key molecular pathways that regulate the immune response. This individual will serve as a strategic regulatory partner to Clinical Development, Clinical Operations, Research, Translational Medicine, CMC, Nonclinical, Quality, Pharmacovigilance, and executive leadership.

ImmunEdge Inc

Senior Director, Regulatory Affairs

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FULL_TIME

With a highly experienced team of experts in immunology and drug development, we are pioneering innovative approaches to target and modulate key molecular pathways that regulate the immune response.   . This individual will serve as a strategic regulatory partner to Clinical Development, Clinical Operations, Research, Translational Medicine, CMC, Nonclinical, Quality, Pharmacovigilance, and executive leadership.

ImmunEdge, Inc

partner JazzHR

Collaborates with fellow Clinical Research Supervisors and Clinical Research Core leadership to develop operational strategies supporting the Clinical Research Core, including staffing models, study portfolio management, workload forecasting, study startup planning, resource allocation, program development, and continuous process improvement. This position provides full operational oversight throughout the study lifecycle, including feasibility assessment, study startup, regulatory implementation, financial oversight, enrollment management, quality assurance, study conduct, and closeout, while also overseeing staffing, performance management, programmatic workflow, and financial stewardship for assigned studies.

UCSF Medical Center

Clinical Research Supervisor

Collaborate with—and serve as a clinical research resource for—cross-functional colleagues (e.g. in clinical operations, statistics, regulatory affairs, medical affairs, health economics outcomes research, commercial, finance) to optimize product development. Guided 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.

Ascendis Pharma

Medical Director, Clinical Development - Job ID: 1930

Workable

The position coordinates activities across research teams and external stakeholders, identifies and resolves project dependencies and operational issues, supports the development of program strategy and major initiatives, and represents QBI programs in interactions with collaborators and partners. Working closely with QBI leadership, Principal Investigators, and internal and external partners, the position independently oversees the planning, implementation, and ongoing management of multi-PI biomedical research programs and projects.

Academic Program Management Officer IV

WORKING CONDITIONS: Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections. This position includes managing device trials for neuromodulation, conducting longitudinal natural history studies, and assisting with various PI-initiated projects involving adult subjects.

Stanford University

Clinical Research Coordinator

Incumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.

Incumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical and health services research studies; acting as the intermediary between services and departments while overseeing data and specimen management; managing and reporting on study results; creating, cleaning, updating, and managing databases and comprehensive datasets and reports; managing Investigator's protocols in the Committee on Human Research online system, and completing renewals and modifications of protocol applications and the implementation of new studies with PI oversight. In addition, the Coordinator will participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; interface with departments to obtain UCSF approval prior to study initiation; complete and maintain all regulatory documents; report study progress to investigators; participate in manuscript, grant, and abstract preparation and submission; and participate in any internal and external audits or reviews of study protocols.

CLIN RSCH CRD

It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository. The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.

Investigator Jobs in Hillsborough, CA

Platform Security Engineer Outset

Director/Senior Director, Clinical Operations 5AM Ventures

Senior Director, Regulatory Affairs ImmunEdge Inc

Senior Director, Regulatory Affairs ImmunEdge, Inc

Clinical Research Supervisor UCSF Medical Center

Medical Director, Clinical Development - Job ID: 1930 Ascendis Pharma

Academic Program Management Officer IV UCSF Medical Center

Clinical Research Coordinator Stanford University

Clinical Research Coordinator UCSF Medical Center

CLIN RSCH CRD UCSF Medical Center

Senior Clinical Research Coordinator UCSF Medical Center

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