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Radionetics Oncology · 2 days ago

VP or SVP of Clinical Development

San Diego, CA

Full-time

Hybrid

Director/Executive

$315K/yr - $415K/yr

6+ years exp

Radionetics Oncology, Inc. is a clinical stage company focused on the discovery and development of novel radiopharmaceuticals for oncology treatments. They are seeking a VP/SVP of Clinical Development to lead clinical trials, provide strategic direction, and collaborate with cross-functional teams to advance their innovative therapies.

Health CareMedicalOncologyPharmaceuticalTherapeutics

Responsibilities

Serve as a medical lead for one or more radioligand therapy programs

Develop and drive the clinical development plan, ensuring alignment with regulatory requirements and the company’s strategic goals

Work closely with the CMO on the design and preparation of clinical trial protocols (first-in-human), statistical analysis plans, and clinical study reports

Provide ongoing medical monitoring and real-time support for clinical trials, including reviewing and interpreting clinical data, assessing safety signals, and determining the medical eligibility of subjects

Perform clinical data review and interpretation, including the preparation of top-line results, integrated summaries of safety and efficacy, and final reports

Serve as a medical expert in interactions with regulatory authorities globally

Prepare and present clinical data during meetings to support regulatory filings and development

Work closely with cross-functional teams, including Research & Discovery, Translational Medicine, Biostatistics, Clinical Operations, Regulatory Affairs, and CMC to ensure seamless program execution, recognizing the unique supply chain and manufacturing needs of RLTs

Establish and maintain relationships with key opinion leaders (KOLs), investigators and clinical site staff to garner clinical insights

Travel to sites to enhance engagement and drive clinical trial enrollment

Lead the preparation of clinical trial results for publication in peer-reviewed journals and presentation at major scientific congresses (e.g., ASCO, ESMO, SNMMI)

Provide internal medical and scientific training to internal teams (e.g., business development, commercial, medical affairs) as needed

Qualification

Oncology drug developmentRadioligand therapy expertiseClinical trial designMedical monitoringRegulatory interactionCross-functional leadershipMedical Doctor (MD)Board certification in OncologyClinical data interpretationPublicationsPresentations

Required

M.D. required

Board Certification/Eligibility in Oncology, Hematology/Oncology, or Nuclear Medicine is highly preferred

Minimum 6-12+ years of industry clinical development experience, with a focus on oncology

Progressive leadership experience in clinical development, with demonstrated ability to define and execute global clinical strategies for complex therapeutics

Deep knowledge of the oncology landscape, including standard of care, translational research, and emerging therapeutic modalities

Proven experience designing, implementing, and medically overseeing first-in-human/ Phase 1 clinical trials

Preferred

Direct experience with the development, clinical application, or regulatory aspects of radiopharmaceuticals, targeted radionuclide therapy, or nuclear medicine

Understanding of the unique safety, handling, and logistics challenges associated with radioligand therapies