Medical Oncologist/Oncology Research Director (Miami, FL)

The START Center for Cancer Research; Miami (FL); Presencial; USD 180 000 - 300 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

401(k) retirement savings with company

Annual bonuses eligibility

Generous paid time off & holidays

Comprehensive medical/dental/vision

Life and disability insurance

Resumo da oferta

The START Center for Cancer Research in Miami seeks a Clinical Principal Investigator (physician-scientist) to oversee the planning, conduct, and regulatory compliance of sponsored early-phase oncology trials. You will guide protocol development, data interpretation, and sponsor communications from our Miami site.

Ideal candidates hold an MD, board certification in hematology/oncology, and have hands-on clinical trial experience with drug development and regulatory understanding.

Qualificações

• MD or equivalent to practice as Principal Investigator.
• Board-certified in hematology and/or medical oncology.
• Clinical trials experience with drug development interest.
• Understanding of GCP, safety reporting, FDA regulations and ethics.

Responsabilidades

• Manage early phase clinical trials with medical direction and protocol reviews.
• Assess feasibility of sponsor inquiries and drive growth through partnerships.
• Lead a matrix team responsible for early phase oncology trials.
• Ensure participant safety, data integrity, and rights/privacy.
• Develop relationships with sponsors and CROs involved in study conduct.
• Provide guidance to clinical operations staff and sponsors.
• Lead quality improvement efforts and foster research excellence.
• Develop strategies to enhance patient recruitment and retention.

Formação académica

MD or equivalent

Board Certification in Hematology/Medical Oncology

Clinical trials experience

GCP, FDA regulations knowledge

Descrição da oferta de emprego

The START Center for Cancer Research ("START") is the world's largestearly phasesite network, fully dedicated tooncologyclinical research. Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access"tocutting edgetrials throughout the UnitedStatesand Europe.

We are seeking a Clinical Principal Investigator. The Clinical Principal Investigator (PI) is a physician-scientist responsible for the overall preparation, conduct, and management of sponsored projects, ensuring compliance with all regulatory requirements and institutional policies. This role will manage the development and execution of clinical trial protocols, contribute to data analysis, and maintain strong communication and alignment with sponsors.

Location: 13400 S.W. 120th St Suite 300-A Miami, Florida 33186

Essential Responsibilities

• Manage early phase clinical trials by providing overarching medical direction and comprehensive medical reviews of protocols in conformance with the investigational plan and good clinical practice.
• Provide medical and scientific feasibility of all new sponsor inquiries driving growth through strategic partnerships.
• Lead and manage a matrix team of responsible for responsible for the conduct of early phase oncology trials.
• Ensure the safety and well-being of all participants in the study at the trial site are protected.
• Ensure data collected at the study site is credible and accurate.
• Ensure the rights, integrity, and confidentiality of all participants in the trial at the site are protected.
• Develop close personal working relationships with Sponsors and Clinical Research Organizations involved in study conduct.
• Provide expert guidance and support to clinical operations research staff and sponsor client.
• Lead continuous quality improvement efforts for clinical research services, integrating best practices and fostering a culture of research excellence.
• Develop and implement strategies to enhance patient recruitment and retention in clinical trials.

Required Education And Experience

• M.D. or equivalent.
• Board Certified in Hematology and/or Medical Oncology.
• Clinical trials experience with a strong interest in drug development.
• Ability to critically analyze clinical scientific data and literature.
• Understanding of GCP principles, safety and adverse event reporting, FDA regulations, and biomedical research ethics.
• A passion for providing excellent clinical care and for working in a collaborative / team-oriented environment.

Preferred Education And Experience

• Previous experience with industry sponsored clinical trials.
• Excellent communication skills, with experience in publishing and presenting at scientific meetings.
• Translational research experience and familiarity with pharmacokinetics and pharmacodynamics.

Best-in-Class Benefits and Perks

• 401(k) retirement savings plan with employer match
• Eligibility for an annual performance bonus, based on role and company results
• Generous paid time off and paid holidays
• Comprehensive medical, dental, and vision coverageand optional insuranceoptions
• Company paid life and disability insurance for added financial protection
• Employee Assistance Program (EAP) providing confidential, no -cost support for you and your family from day one
• Flexible FSA and HSA plans to support your financial wellness
• Commitment to a supportive environment that values balance, wellbeing, and flexibility
• We'recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you'lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world's largest roster of early-phase principal investigators across its Network of clinical trial sites.

Learn more at STARTresearch.com.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.