BioSpace
Clinical Research Medical Director, Neurology
BioSpace, Washington, District of Columbia, us, 20022
Clinical Research Medical Director, Neurology
BioSpace is seeking a Clinical Research Medical Director, Neurology to serve as a clinical expert for the development and communication of global scientific and medical evidence plans.
What You Will Do
Provide oversight of LCM clinical development with input on global strategy.
Support cross‑functional and global collaborations to integrate broad medical, regulatory, safety, scientific, and commercial access and value input into the development program(s).
Participate and provide clinical input into safety and regulatory interactions.
Interpret and communicate clinical trial data.
Author or review Clinical Study Reports, publications, and regulatory submissions.
Develop key opinion leaders and make scientific presentations at advisory boards, key scientific meetings and external committee meetings as delegated by the Global Development Lead.
Identify new clinical research opportunities.
Support in‑licensing, out‑licensing activities and partner relationships; support product lifecycle management for new indications as directed by the Global Development Lead.
Provide clinical content input to materials to be used in Scientific Affairs and the Commercial Organization.
Travel approximately 10% of the time.
This is a potential managerial role; prior experience seeking and developing talent is a plus.
Basic Qualifications
MD or DO degree from an accredited medical school.
At least 2 years of clinical research experience and/or basic science research.
Preferred Qualifications
MD with strong and versatile clinical development experience in Inflammation, and accreditation in a relevant sub‑specialty.
Three or more years of clinical development experience and/or basic science research combined with clinical teaching and patient care activities.
Clinical development experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company).
Experience in development lifecycle management to include development strategy creation for large programs from early development through late development and commercialization.
Involved in filing activities as part of moving the program through the development lifecycle.
Key relationship development and collaboration with the expansive commercial and medical teams internal and external partners and key opinion leaders.
Previous management experience of clinical development professionals.
Benefits
A comprehensive employee benefits package, including a retirement and savings plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance and flexible spending accounts.
A discretionary annual bonus program.
Stock‑based long‑term incentives.
Award‑winning time‑off plans.
Flexible work models, including remote and hybrid work arrangements where possible.
Equal Opportunity Employer Amgen is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status or any other basis protected by applicable law.
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What You Will Do
Provide oversight of LCM clinical development with input on global strategy.
Support cross‑functional and global collaborations to integrate broad medical, regulatory, safety, scientific, and commercial access and value input into the development program(s).
Participate and provide clinical input into safety and regulatory interactions.
Interpret and communicate clinical trial data.
Author or review Clinical Study Reports, publications, and regulatory submissions.
Develop key opinion leaders and make scientific presentations at advisory boards, key scientific meetings and external committee meetings as delegated by the Global Development Lead.
Identify new clinical research opportunities.
Support in‑licensing, out‑licensing activities and partner relationships; support product lifecycle management for new indications as directed by the Global Development Lead.
Provide clinical content input to materials to be used in Scientific Affairs and the Commercial Organization.
Travel approximately 10% of the time.
This is a potential managerial role; prior experience seeking and developing talent is a plus.
Basic Qualifications
MD or DO degree from an accredited medical school.
At least 2 years of clinical research experience and/or basic science research.
Preferred Qualifications
MD with strong and versatile clinical development experience in Inflammation, and accreditation in a relevant sub‑specialty.
Three or more years of clinical development experience and/or basic science research combined with clinical teaching and patient care activities.
Clinical development experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company).
Experience in development lifecycle management to include development strategy creation for large programs from early development through late development and commercialization.
Involved in filing activities as part of moving the program through the development lifecycle.
Key relationship development and collaboration with the expansive commercial and medical teams internal and external partners and key opinion leaders.
Previous management experience of clinical development professionals.
Benefits
A comprehensive employee benefits package, including a retirement and savings plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance and flexible spending accounts.
A discretionary annual bonus program.
Stock‑based long‑term incentives.
Award‑winning time‑off plans.
Flexible work models, including remote and hybrid work arrangements where possible.
Equal Opportunity Employer Amgen is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status or any other basis protected by applicable law.
#J-18808-Ljbffr