Senior Medical Director (Walpole)
Harris & Co Executive Search has been retained on a Senior Medical Director opportunity to be based in Massachusetts.
Our client is a highly regarded biotech within the Endocrinology space who have raised significant capital this year and are now looking to onboard a physician to lead their clinical programs.
If you are physician with a passion for the Endocrinology space then please apply below or reach out to me at email protected DescriptionAs a key member of Clinical Development team, the Sr.
Medical Director will provide strategic direction and development oversight for clinical development programs.
S/he will lead relevant medical responsibilities, providing insight, direction and regulatory alignment.
Collaborating closely with various members of cross-functional teams, s/he will directly guide the successful execution of programs against goals, staying close to the operational tasks with a hand-on approach.
S/he will serve as an internal advisor and go-to resource for medical and scientific inquiries.
Furthermore, the Director will develop and maintain relationships externally with the scientific community through participating in Advisory Boards, Professional Associations, Professional Meetings and Conferences, etc.
S/he will successfully lead teams and manage budgets as assigned.
Primary Responsibilities Provide medical direction and review at various phases of clinical development Lead and implement an orchestrated external stakeholder engagement program Lead and implement key external stakeholder advisory activities that pertain to broad medical strategy Oversee the effective execution of clinical trials, developing and maintaining investigator relationships on an ongoing basis and ensuring timely study-subject recruitment in line with study goals Serve as a key team member, providing input on early stage prototype programs Develop and execute animal and clinical study designs, developing the associated protocols in close collaboration with cross functional teams and leading the interpretation of related data Lead clinical safety oversight in partnership with internal and external stakeholders Oversee the medical review and sign off of promotional materials Participate in, and provide input for, the publications strategy Oversee the planning and execution of medical & clinical education programs, maintaining consistent and value-based measurements of all medical education activities Provide input on confidential new business development opportunities as appropriate Maintain team budgets, planning and tracking the related activities Manage vendors and monitor vendor performance Lead/co-lead cross-functional project teams within a matrix organizational structure.
Education or Certification Requirements MD degree and related active licenses & accreditation Board certification within a field related to metabolism a plus Professional Work Experience 8
years of successful and progressive global clinical development experience within related industries Experience in relevant clinical practice, research and academia Experience with industry regulations governing medical activities and medical regulatory processes Applicable experience in biotech, pharmaceutical and/or medical device industries preferred.
Qualifications and Skills Hands on experience managing projects related to the launch of products within related industries Experience leading and managing teams Experience working in small-company work environment Demonstrated successful program management including the ability to manage multiple tasks and priorities Track record of challenging oneself to enhance medical and scientific knowledge Full understanding of GCP and other relevant regulatory knowledge #J-18808-Ljbffr Recommended Skills Advertising Biotechnology Business Development Clinical Practices Clinical Works Consulting Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
Our client is a highly regarded biotech within the Endocrinology space who have raised significant capital this year and are now looking to onboard a physician to lead their clinical programs.
If you are physician with a passion for the Endocrinology space then please apply below or reach out to me at email protected DescriptionAs a key member of Clinical Development team, the Sr.
Medical Director will provide strategic direction and development oversight for clinical development programs.
S/he will lead relevant medical responsibilities, providing insight, direction and regulatory alignment.
Collaborating closely with various members of cross-functional teams, s/he will directly guide the successful execution of programs against goals, staying close to the operational tasks with a hand-on approach.
S/he will serve as an internal advisor and go-to resource for medical and scientific inquiries.
Furthermore, the Director will develop and maintain relationships externally with the scientific community through participating in Advisory Boards, Professional Associations, Professional Meetings and Conferences, etc.
S/he will successfully lead teams and manage budgets as assigned.
Primary Responsibilities Provide medical direction and review at various phases of clinical development Lead and implement an orchestrated external stakeholder engagement program Lead and implement key external stakeholder advisory activities that pertain to broad medical strategy Oversee the effective execution of clinical trials, developing and maintaining investigator relationships on an ongoing basis and ensuring timely study-subject recruitment in line with study goals Serve as a key team member, providing input on early stage prototype programs Develop and execute animal and clinical study designs, developing the associated protocols in close collaboration with cross functional teams and leading the interpretation of related data Lead clinical safety oversight in partnership with internal and external stakeholders Oversee the medical review and sign off of promotional materials Participate in, and provide input for, the publications strategy Oversee the planning and execution of medical & clinical education programs, maintaining consistent and value-based measurements of all medical education activities Provide input on confidential new business development opportunities as appropriate Maintain team budgets, planning and tracking the related activities Manage vendors and monitor vendor performance Lead/co-lead cross-functional project teams within a matrix organizational structure.
Education or Certification Requirements MD degree and related active licenses & accreditation Board certification within a field related to metabolism a plus Professional Work Experience 8
years of successful and progressive global clinical development experience within related industries Experience in relevant clinical practice, research and academia Experience with industry regulations governing medical activities and medical regulatory processes Applicable experience in biotech, pharmaceutical and/or medical device industries preferred.
Qualifications and Skills Hands on experience managing projects related to the launch of products within related industries Experience leading and managing teams Experience working in small-company work environment Demonstrated successful program management including the ability to manage multiple tasks and priorities Track record of challenging oneself to enhance medical and scientific knowledge Full understanding of GCP and other relevant regulatory knowledge #J-18808-Ljbffr Recommended Skills Advertising Biotechnology Business Development Clinical Practices Clinical Works Consulting Apply to this job.
Think you're the perfect candidate? Apply on company site Estimated Salary: $20 to $28 per hour based on qualifications.
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