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Director Prostate Cancer Jobs (NOW HIRING)

AstraZeneca

Medical Lead - Prostate

Gaithersburg, MD · On-site

We are seeking a Medical Lead, Prostate Cancer to join US Medical Affairs in Gaithersburg, Maryland ... stakeholders without direct authority. * Excellent written, verbal, interpersonal, and ...

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Director Prostate Cancer information

What is the difference between Director Prostate Cancer vs Medical Director Oncology?

AspectDirector Prostate CancerMedical Director Oncology
CredentialsMedical degree, oncology specialization, research experienceMedical degree, oncology specialization, leadership experience
Work EnvironmentResearch institutions, hospitals, cancer centersHospitals, healthcare organizations, pharmaceutical companies
Industry UsageFocuses on prostate cancer research and treatment programsOversees oncology services and clinical programs across cancer types

The main difference is that the Director Prostate Cancer specializes specifically in prostate cancer research and treatment, while the Medical Director Oncology oversees broader oncology services across multiple cancer types. Both roles require medical credentials and leadership skills but differ in scope and focus.

How does the Director Prostate Cancer collaborate with cross-functional teams to drive successful patient outcomes?

As a Director Prostate Cancer, collaboration with cross-functional teams—including clinical, research, medical affairs, and marketing departments—is essential to ensure comprehensive patient care and successful program implementation. This role frequently leads multidisciplinary meetings to align research initiatives, clinical trial strategies, and patient education efforts. Effective communication, leadership, and decision-making are key to managing diverse teams and integrating feedback from various stakeholders. Building strong partnerships across departments not only enhances patient outcomes but also supports the development of innovative treatment protocols.

What does a Director of Prostate Cancer do?

A Director of Prostate Cancer is a senior leader responsible for overseeing clinical, research, and administrative aspects related to prostate cancer within a healthcare organization or research institution. They coordinate multidisciplinary teams, guide treatment protocols, and ensure high-quality patient care. Additionally, they may contribute to research initiatives, community outreach, and the development of educational programs for patients and staff. Their role often involves strategic planning, policy implementation, and collaboration with stakeholders to improve prostate cancer outcomes.

What are the key skills and qualifications needed to thrive as a Director Prostate Cancer, and why are they important?

A Director Prostate Cancer typically requires an advanced degree in medicine or healthcare, substantial experience in oncology, and proven leadership in clinical or research settings. Familiarity with cancer treatment protocols, clinical trial management systems, and regulatory compliance (such as FDA guidelines) is essential. Exceptional communication, strategic planning, and team leadership skills distinguish top performers in this role. These competencies ensure effective program management, high-quality patient care, and advancement of research or treatment initiatives.
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Director Prostate Cancer jobs near you
Infographic showing various Director Prostate Cancer job openings in the United States as of May 2026, with employment types broken down into 85% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.
Medical Director/Senior Medical Director, Clinical Development (Prostate)

Medical Director/Senior Medical Director, Clinical Development (Prostate)

ORIC Pharmaceuticals

San Diego, CA • On-site

$270K - $320K/yr

Full-time

Posted 4 days ago

Job description

Company Description
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.
We are seeking an experienced oncology physician to serve as a Medical Director or Senior Medical Director at ORIC Pharmaceuticals. This role provides medical leadership across one or more clinical development programs, with a primary focus on late-stage (registration-enabling) clinical trials. The position plays a critical role in shaping clinical strategy, ensuring scientific rigor, guiding regulatory interactions, and advancing programs from study design through regulatory submission.
The Medical Director will work in close partnership with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, Safety/Pharmacovigilance, Translational Medicine, and Medical Affairs. The role requires strong strategic thinking, hands-on execution, and the ability to lead effectively in a fast-paced biotech environment.
Job Description
Clinical and Medical Leadership
  • Serve as the medical lead for one or more oncology programs across all phases of development
  • Provide medical monitoring oversight for global clinical trials, including Phase 1-3 and registration-enabling studies.
  • Act as the primary medical expert for internal teams and external stakeholders
  • Represent the company in interactions with investigators, key opinion leaders, advisory boards, and regulatory authorities (e.g., FDA, EMA/CHMP)

Clinical Development Strategy and Execution
  • Partner with clinical scientists in the design and execution of clinical protocols, amendments, investigator brochures, study reports, abstracts, and manuscripts
  • Partner with biostatistics to define study endpoints, statistical plans, and data analyses
  • Ensure scientific rigor, data integrity, and patient-centric decision-making throughout development
  • Maintain strong clinical and scientific competitive intelligence through ongoing engagement with the oncology community and key scientific meetings

Cross-Functional Collaboration
  • Work closely with Clinical Operations and CROs to support trial execution and operational excellence
  • Collaborate with Regulatory Affairs on global regulatory strategy and submissions (e.g., INDs, NDAs, MAA)
  • Partner with Safety/Pharmacovigilance to review adverse events, monitor safety signals, and support benefit-risk assessments
  • Contribute to biomarker and translational strategies in collaboration with preclinical and translational teams

External Communication and Scientific Contribution
  • Support investigator engagement, site training, and advisory board activities
  • Contribute to abstracts, manuscripts, posters, and scientific presentations
  • Participate in scientific conferences and external meetings as a medical representative of the company

Leadership and Organizational Contribution
  • Lead and influence cross-functional teams in a matrixed environment
  • Contribute to the overall clinical development strategy and culture of scientific excellence to ensure alignment with ORIC's values, SOPs, and ethical standards

Qualifications
Education and Training
  • MD required
  • Board certified or board eligible in Oncology or Hematology/Oncology

Experience
  • 5+ years of experience in oncology clinical development, with increasing responsibility; experience in small-mid biotech environment is a plus
  • Demonstrated experience leading or contributing to late-phase oncology clinical trials; particularly in prostate cancer is desired
  • Strong understanding of global clinical development pathways and regulatory requirements (FDA, EMA, ICH/GCP)
  • Familiarity with current medical practice in GU oncology with development experience is a major plus
  • Prior experience as a principal investigator or academic clinician is a plus

Additional Information
The anticipated salary range for director level candidates who will work in our San Diego location is between $270,000-$320,000. The final salary offered to a successful candidate will be dependent on several factors that may include, but are not limited to, degree type (MD vs. non-MD), title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors.
ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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