Vice President, Clinical Development (Oncology)
$360k - $425kAllogene Therapeutics
About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. 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. About the role: The Vice President, Clinical Development will work across functions including Clinical Operations, Regulatory Affairs, Translational Science, Safety, Quality and others in supporting our efforts in this exciting new area of cancer immunotherapy. This role is based out of Allogene’s headquarters in South San Francisco, CA. Remote candidates will be evaluated based on suitability for the position along with frequent travel to Allogene’s South San Francisco or Los Angeles office. Responsibilities include, but are not limited to: Lead the Oncology Clinical Development team, ensuring that the performance of employees is proactively managed and they are coached, trained and developed in order to maximize their contribution Accountable for the company’s oncology clinical development including clinical trials execution and data collection and analysis Responsible for development of clinical protocols to support the company’s product strategy, data collection and management and final reports development in compliance with appropriate standard operating procedures, regulatory and medical standards Collaborate with our head of medical affairs around scientific communication of our clinical data and execution of oncology congress planning and representation and advisory boards Key member and/or leader of the oncology asset teams in which asset strategy is developed and its execution is overseen Represent oncology clinical development at senior executive meetings Identification and communication around opportunities for change and alignment and leadership toward change when necessary Influence and/or develop broad-based programs and initiatives to meet executive level vision and mission Collaborate with functional leaders to set strategy and shared objectives and interactions with health agencies and vendors (including CROs) Represent Allogene at meetings with regulatory authorities and third parties such as licensing or co-development partners, consultants, etc. Other duties as assigned Position Requirements & Experience: MD; completion of residency and oncology fellowship with extensive industry leadership experience in developing oncology treatments; cell therapy experience is highly desirable Global experience in clinical trial as well as post-marketing setting (cell therapy experience highly preferred but not required) Strong knowledge and understanding of US, EU and Asian development requirements and general regulatory expectations Ability to evaluate and manage CROs and other vendors Excellent organizational skills and an ability to prioritize effectively to deliver results within aggressive timelines with the ability to work independently and as part of a team Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment Ability to communicate with internal and external physicians to evaluate specific safety events Candidates must be authorized to work in the U.S We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected salary range for this role is $360,000 to $425,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. #J-18808-Ljbffr Allogene Therapeutics
$342.8k
Job Description The Associate Vice President (AVP) is primarily... ...for planning and directing clinical research activities involving new or marketed drugs for oncology indications. The AVP manages... ...the entire cycle of clinical development, including study design, initiation...SuggestedWorldwide$336k - $405k
...Vice President, Clinical Development Reporting to the Chief Medical Officer (CMO), and located at our headquarters in South San Francisco, the Vice... ...M.D. degree; advanced knowledge in hematology/oncology required. Board certification in hematology or oncology...Suggested$234k
...several key therapeutic areas including immunology, oncology and neuroscience - and products and services... ..., planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-...SuggestedLocal area$399.6k - $427.5k
...Biosciences is a biopharmaceutical company advancing a late‑stage clinical platform of novel therapies for people living with... ...trials and are headquartered in Brisbane, CA. Position Vice President, Clinical Development - Neuroscience As a key leader, you will drive the...SuggestedRemote workFlexible hours$360k - $420k
...its pipeline of LYTAC extracellular protein degraders to the clinic. Lycia is headquartered in South San Francisco. Visit for more... ...a highly motivated, innovative, and collaborative clinical development leader to join our team in advancing our pipeline of LYTAC degraders...SuggestedContract workFlexible hours- ...Nurix Therapeutics is seeking a Vice President, Medical Affairs, Hematology‑Oncology to build, expand, and lead a best... ...the company’s transition from a clinical‑stage biotechnology company... ...advances into late‑stage clinical development. This executive will provide strategic...
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...delivering meaningful therapeutics to patients. The Vice President of Market Access will lead the strategy, development, and execution of U.S. market access... ...Commercial, Patient Advocacy, Medical Affairs, Clinical Development, and Regulatory to ensure access considerations...Local area$257.89k - $348.91k
Executive Director, Oncology Research What you will do Lets do this. Lets change the world... ...you will drive the discovery and development of novel therapeutics for solid tumors and... ...from target discovery and validation to clinical candidate selection, and supporting clinical...WorldwideFlexible hours$360k - $420k
Lycia Therapeutics is seeking a Clinical Development Leader to advance their drug pipeline in South San Francisco. This role involves overseeing mid- and late-phase clinical trials, ensuring regulatory compliance, and collaborating with various teams. Ideal candidates...$330k - $375k
...playing a key role within the Pharmaceutical Development & Manufacturing organization at the... ...the vision and strategy for clinical supply operations and launch and commercialization... ...anticipates the base salary for the Vice President, Clinical Supply Management to range from...Contract workLocal areaWorldwide$300k - $420k
...This clinical-stage biotechnology company is changing the treatment... .... They are seeking a Senior Vice President of Regulatory Affairs to... ...You will proactively shape development strategy, lead health authority... ...strategy for the company’s oncology portfolio, including health...Local areaRelocationFlexible hours3 days per week- insitro.com is seeking a Chief Medical Officer (CMO) in South San Francisco to lead clinical development strategies. This role demands a strong background in clinical trials and regulatory affairs, underpinned by 20+ years in biotech. The CMO will spearhead innovative...
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...Vice President Corporate Communications & Investor Relations South San Francisco Alumis... ...Communications and Investor Relations will lead the development and implementation of Alumis' strategic... .../ PR, commercial, investor relations, clinical, medical affairs, research and HR. They...Local area- Biogen is seeking a Head of Clinical Pharmacology & Pharmacometrics based in San Francisco to lead strategic oversight across our development portfolio. This role requires extensive leadership experience in Clinical Pharmacology and Pharmacometrics, ensuring scientific...
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Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers.... ...RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will...$190.6k - $405.9k
...Department of Surgery, Division of Surgical Oncology, University of California, San Francisco... ...Chief of Colorectal Surgery leads all clinical, academic, research, and administrative... ...with all the following: Program development (strategic growth). Program leadership...Full timeLocal areaFlexible hoursShift work- ...both the regulatory function and broader development strategy. The Role We're looking... ...infrastructure Partner cross‑functionally with Clinical Development, CMC, Nonclinical, and... ..., processes) ~ Strong background in oncology; biologics experience is highly...
$265k - $331k
Revolution Medicines is a late‑stage clinical oncology company developing novel targeted therapies for patients with RAS‑addicted cancers.... ...and executes the global GCP quality strategy across clinical development programs. The role ensures compliance with regulatory...Full timeContract work$265k - $331k
...Overview Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted... ...RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will...Full timeContract workLocal area$422k
...compliance, product quality, patient safety, and regulatory excellence. Shapes long‑term regulatory and quality strategies that support development, commercialization, lifecycle management, geographic expansion, and sustainable business growth. Serves as a key member of the...Local areaWorldwide- Initial Therapeutics, Inc. is seeking an Executive Director of Oncology Research to lead the discovery and development of transformative therapeutics for cancer. This high-visibility role emphasizes strategy, team leadership, and impactful research. The ideal candidate...
- ...challenges faced by biopharma companies. The ideal candidate has a strong product management background with a deep understanding of clinical development, excellent problem-solving skills, and a passion for health innovation. Unlearn.AI offers substantial benefits including...
$265k - $300k
Executive Director, Clinical Quality Assurance Boston; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical‑... ...undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics...Work at officeRemote work- Allergan is seeking a Clinical Development Lead in San Francisco, CA to oversee clinical trials and develop strategies for product development. The ideal candidate will have an M.D. or equivalent and at least 5 years of industry experience. This role involves ensuring...
- ...biomarkers, and surrogate endpoints; advise leadership on reimbursement risks. Evidence & value: define payer value proposition (clinical/biomarker/RWE); build HEOR models and access-focused evidence for coverage and AA‑to‑full conversion; ensure endpoints/RWE...
$330k - $375k
...International Executive Service Corps is seeking a Vice President for Clinical Supply Management to lead the Nektar supply chain function in San Francisco. The role demands extensive experience in the pharmaceutical sector and expertise in managing clinical and commercial...$300k - $400k
...compound, envudeucitinib (ESK-001), has demonstrated compelling clinical results in psoriasis and is advancing through pivotal studies... ...Medical Director or Senior Medical Director to lead clinical development strategy and execution for Phase 1 and Phase 2 studies in neurology...Remote work$315k - $340k
...Olema Oncology is a clinical-stage biopharmaceutical company committed to transforming the standard... ...what's beyond . About the Role Vice President, Quality Assurance The... ...lifecycle, including clinical development, manufacturing, pharmacovigilance, and...Full timeWork at officeFlexible hours$249.6k
...computational sciences are transforming drug discovery and development. Roche’s Research and Early Development... ..., and computational biology approaches in Oncology while developing our projects through the pre‑clinical and clinical stages. This role is a leader of leaders...Local areaWorldwideRelocation package$265k - $331k
...San Francisco seeks an Executive Director of GCP QA to oversee the global GCP quality strategy and ensure compliance across clinical development programs. The candidate will lead a QA team, oversee vendor quality management, and engage with regulatory authorities. With...
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