GSK

Medical Director, Vaccines

Employer
GSK
Location
Philadelphia, PA
Salary
Competitive
Posted
May 28 2021
Ref
291657
Organization Type
Pharma
Site Name: USA - Pennsylvania - Philadelphia Posted Date: May 28 2021 As Vaccines Medical Director you will be able to set an inclusive (blending patient needs, external trends and GSK science) vision and oversee and drive strategic execution. Key Responsibilities; Leads defined US medical affairs work for Meningococcal Vaccine portfolio and supporting global franchise, clinical development, US medical matrix team(s) and US medical commercial strategy team(s). Contributes to the development and execution of the US Medical Affairs Plan and the medical sections for the strategic launch plan for one or more vaccines. Integrates US environment and medical voice of customer (patients, providers, payers) into medical affairs strategy. Deeply understands, interprets and applies the external environment and competitive knowledge in all medical plans and is able to define the medical story for the patient. Ensures US needs for medical and health outcomes evidence generation are represented and incorporated into the global medical work. Recommends scientifically appropriate measures within health outcomes research over the lifecycle of the Meningococcal Vaccine Portfolio to meet US reimbursement needs. Contributes to the design and delivery of Phase IIIB/IV studies in collaboration with global franchises, acts as medical monitor where appropriate and manages US funded investigator sponsored studies as appropriate. Leads appropriate US scientific engagement between GSK and external communities in order to advance scientific and medical understanding including the appropriate development and use of our vaccines, the management of disease, and patient care. Ensures US external experts are appropriately engaged over the life cycle of the Meningococcal Vaccine Portfolio in close collaboration with field medical. Partners with all stakeholders to ensure delivery of all assigned medical activities to support life cycle management, ensuring integrity of scientific content. Applies sound medical governance for all activities and is accountable for medical governance sign off. Works closely with safety, regulatory, and manufacturing to ensure best benefit-risk assessment and ability to quickly integrate relevant changes. Serves as US medical affairs point for all safety issues. Accountable for maintaining deep product and disease area expertise, and maintaining a deep understanding of patient and physician interactions and clinical decision making and impact. May include accountability of other medical staff for execution of work and people development for one or more medicine(s). Leads/contributes to copy approval process. Supports the USMAL or Medical Affairs TAH as needed. Serves as Local Medical Lead (LML) and provides local (US/Canadian specific) support to the study design; provides medical/scientific leadership to the local study conduct team and manages all local medical activities required before study start, during the study and after study completion and analysis; provides input on local risk management activities and medical oversight on study quality. Basic Qualifications: Medical degree: preference for specialism in Pediatrics or Infectious Diseases. Background in the scientific/pharmaceutical industry within clinical development or medical affairs Experience running clinical trials Excellent communications and leadership skills: able to effectively communicate written and verbal scientific data and to understand the clinical implications of the data. Experience working in matrix teams. Skilled in leveraging available resources to drive business improvement. Demonstrated ability of strategic thinking, project management, and leadership/management Demonstrated ability to work across boundaries and geographies effectively Ability to navigate complex organization matrices, interpretation and translation of evidence and challenging situations to work through to effective solutions If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

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