Medical Director, Neurology
Redwood City, CAFull-time
242K–294K a year
Behavioral Health Market Context
Apply Nowvia Marit Health
Job Description
ill play a key role in advancing Corcept's mission to discover and develop novel treatments for serious unmet medical needs through cortisol modulation.
Responsibilities
• Act as a clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
• Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
• Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
• Design, develop and, implement clinical studies for the applicable drug candidate, from Phase I through Phase III
• Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
• Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
• Acts to 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
Compensation
• The pay range that the Company reasonably expects to pay for this headquarters-based position is $242,000 - $294,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Requirements
• Demonstrate strong clinical and scientific knowledge
• Excellent communication skills with proven leadership experience and the ability to interact in a cross functional environment
• Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities
• MD, board-certified (or eligible), preferably in Neurology
• 2+ years' clinical development experience in the biotechnology/pharmaceutical industry or an academic clinical trial unit
• A proven track record of scholarly clinical research demonstrated by publications in top-tier journals
• Applicants must be currently authorized to work in the United States on a full-time basis
Responsibilities
• Act as a clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
• Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
• Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
• Design, develop and, implement clinical studies for the applicable drug candidate, from Phase I through Phase III
• Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
• Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
• Acts to 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
Compensation
• The pay range that the Company reasonably expects to pay for this headquarters-based position is $242,000 - $294,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Requirements
• Demonstrate strong clinical and scientific knowledge
• Excellent communication skills with proven leadership experience and the ability to interact in a cross functional environment
• Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities
• MD, board-certified (or eligible), preferably in Neurology
• 2+ years' clinical development experience in the biotechnology/pharmaceutical industry or an academic clinical trial unit
• A proven track record of scholarly clinical research demonstrated by publications in top-tier journals
• Applicants must be currently authorized to work in the United States on a full-time basis
Qualifications
- •Demonstrate strong clinical and scientific knowledge
- •Excellent communication skills with proven leadership experience and the ability to interact in a cross functional environment
- •Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities
- •MD, board-certified (or eligible), preferably in Neurology
- •2+ years' clinical development experience in the biotechnology/pharmaceutical industry or an academic clinical trial unit
- •A proven track record of scholarly clinical research demonstrated by publications in top-tier journals
- •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 $242,000 - $294,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education
Responsibilities
- •Corcept is seeking a Medical Director to support the ongoing and planned execution of ALS trials and contribute to new indication selection and clinical development planning for Neurology
- •This role involves acting as a clinical scientist and subject matter expert, providing scientific oversight, and designing and implementing clinical studies from Phase I through Phase III
- •The Medical Director will play a key role in advancing Corcept's mission to discover and develop novel treatments for serious unmet medical needs through cortisol modulation
- •Act as a clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
- •Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
- •Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
- •Design, develop and, implement clinical studies for the applicable drug candidate, from Phase I through Phase III
- •Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
- •Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
- •Acts to 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
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