Medical Director, Oncology
298K–351K a year
Behavioral Health Market Context
Apply Nowvia Marit Health
Job Description
l data and collaborating with various internal and external stakeholders.
Responsibilities
• Design and implement Phase I to III clinical studies
• Develop and participate in the writing and review of protocols, investigator brochures, study reports, and other clinical and regulatory documents
• Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
• Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
• Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports
• Provide medical oversight and safety monitoring for ongoing clinical trials, including participation in SAE reporting and serving on the safety committee
• Play a key role in the analysis, interpretation, and delivery of high-quality clinical data
• Interact with principal investigators and opinion leaders to facilitate clinical trials research
Compensation
• The pay range that the Company reasonably expects to pay for this headquarters-based position is $298,000-$350,600
Requirements
• MD, board-certified (or eligible)
• Expertise in Oncology
• A strong track record of scientific activity, demonstrated by publications in top tier journals
• At least 6+ years of relevant clinical development experience
• Relevant basic and/or clinical research experience in academic settings is viewed favorably
• Demonstrate strong clinical and scientific knowledge
• Is an excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
• Feel comfortable in a fast-paced and nimble small company environment and able to adjust workload based upon changing priorities
• Applicants must be currently authorized to work in the United States on a full-time basis
Responsibilities
• Design and implement Phase I to III clinical studies
• Develop and participate in the writing and review of protocols, investigator brochures, study reports, and other clinical and regulatory documents
• Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
• Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
• Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports
• Provide medical oversight and safety monitoring for ongoing clinical trials, including participation in SAE reporting and serving on the safety committee
• Play a key role in the analysis, interpretation, and delivery of high-quality clinical data
• Interact with principal investigators and opinion leaders to facilitate clinical trials research
Compensation
• The pay range that the Company reasonably expects to pay for this headquarters-based position is $298,000-$350,600
Requirements
• MD, board-certified (or eligible)
• Expertise in Oncology
• A strong track record of scientific activity, demonstrated by publications in top tier journals
• At least 6+ years of relevant clinical development experience
• Relevant basic and/or clinical research experience in academic settings is viewed favorably
• Demonstrate strong clinical and scientific knowledge
• Is an excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
• Feel comfortable in a fast-paced and nimble small company environment and able to adjust workload based upon changing priorities
• Applicants must be currently authorized to work in the United States on a full-time basis
Qualifications
- •MD, board-certified (or eligible)
- •Expertise in Oncology
- •A strong track record of scientific activity, demonstrated by publications in top tier journals
- •At least 6+ years of relevant clinical development experience
- •Relevant basic and/or clinical research experience in academic settings is viewed favorably
- •Demonstrate strong clinical and scientific knowledge
- •Is an excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
- •Feel comfortable in a fast-paced and nimble small company environment and able to adjust workload based upon changing priorities
- •Applicants must be currently authorized to work in the United States on a full-time basis
Benefits
- •The pay range that the Company reasonably expects to pay for this headquarters-based position is $298,000-$350,600
Responsibilities
- •Corcept is seeking a physician to design and implement clinical studies from Phase I to III, focusing on hypercortisolism and oncology treatments
- •This role involves providing scientific and medical oversight for clinical trials, acting as a subject matter expert, and contributing to regulatory discussions and document development
- •The successful candidate will play a key role in analyzing clinical data and collaborating with various internal and external stakeholders
- •Design and implement Phase I to III clinical studies
- •Develop and participate in the writing and review of protocols, investigator brochures, study reports, and other clinical and regulatory documents
- •Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
- •Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
- •Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports
- •Provide medical oversight and safety monitoring for ongoing clinical trials, including participation in SAE reporting and serving on the safety committee
- •Play a key role in the analysis, interpretation, and delivery of high-quality clinical data
- •Interact with principal investigators and opinion leaders to facilitate clinical trials research
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