Medical Director/Sr Medical Director Early Clinical Development

Job content

• Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilence and clinical operations
• Interacts with global regulatory bodies including the FDA, EMA and PMDA to accomplish tasks related to oncology product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs)
• Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, investigator brochure, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans
• Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies
• Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development
• Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development
• Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders
• Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies
• Works in partnership with medical affairs for successful launch of future anti¬neoplastic agents
• Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents
• Provides guidance for successful implementation and accomplishment of investigator initiated trials related to product development and life cycle management of a compound
• Contribute positively to a strong culture of business integrity and ethics
• Act within compliance and legal requirements as well as within company guidelines
  

• M.D. or D.O. degree with a minimum of 3 - 5 years of experience (6+ years - senior) in oncology drug development in a biotechnology or pharmaceutical company, clinical research experience in academia also acceptable
• Board certified or eligible in Oncology preferred
• Experience with early phase oncology trials
• Excellent written and oral communication skills
• Ability to multi-task and work in a face paced environment
  

• Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilence and clinical operations
• Interacts with global regulatory bodies including the FDA, EMA and PMDA to accomplish tasks related to oncology product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs)
• Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, investigator brochure, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans
• Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies
• Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development
• Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development
• Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders
• Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies
• Works in partnership with medical affairs for successful launch of future anti¬neoplastic agents
• Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents
• Provides guidance for successful implementation and accomplishment of investigator initiated trials related to product development and life cycle management of a compound
• Contribute positively to a strong culture of business integrity and ethics
• Act within compliance and legal requirements as well as within company guidelines
• Requirements
• M.D. or D.O. degree with a minimum of 3 - 5 years of experience (6+ years - senior) in oncology drug development in a biotechnology or pharmaceutical company, clinical research experience in academia also acceptable
• Board certified or eligible in Oncology preferred
• Experience with early phase oncology trials
• Excellent written and oral communication skills
• Ability to multi-task and work in a face paced environment
  
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

We Respect Your Privacy

Learn more at: http://www.incyte.com/privacy-policy

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here .

You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.

You can learn more about Incyte’s data protection practices here . By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable).

Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.