The Global Director Medical Affairs (GDMA) is responsible for driving execution of scientific & medical affairs plans for HPV vaccines in key countries and regions. They are impactful members of HPV Vaccines Medical Affairs Team, Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with global Commercial, Center of Real-World Evidence (CORE), Policy and Market Access to address opportunities in key countries. They engage with their network of scientific leaders and decision makers.
Primary activities
Drives execution of the annual scientific & medical plan with medical affairs colleagues from key countries and regions.
Is impactful member of the HPV Vaccines Medical Affairs Team, Product Development Team sub-teams (Clinical, Value Evidence, Commercial, Publications and Label) and Global Human Health commercialization teams.
Contributes to the development of a single global scientific communications platform.
Consolidates actionable medical insights from countries and regions
Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about our company\'s emerging science
Organizes global expert input events to answer our company\'s questions how to develop and implement new medicines/vaccines: advisory boards and expert input forums
Aligns plans and activities with Global Human Health (commercial) executive directors
Organizes global symposia and educational meetings
Supports key countries with the development of local data generation study concepts and protocols
Reviews investigator-initiated study proposals from key countries prior to headquarters submission (ex-USA)
Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of our company\'s medicines/vaccines
Skills:
Required
MD, PhD or PharmD (MD preferred) and recognized medical expertise
Experience in country, regional or global Medical Affairs, Public Health or Clinical Development
Strong prioritization and decision-making skills
In a matrix environment, able to effectively collaborate with partners across divisions
Excellent interpersonal, analytical, communication (written as well as oral), in addition to results oriented project management skills
Preferred
Three+ years medical affairs experience with proven track record of contribution to medical affairs strategies
Scientific leadership and relationships with other key stakeholders (payers, public groups, government officials, medical professional organizations) related to HPV vaccination.
Note: Although this position is based in Pennsylvania, residence in Pennsylvania is not required.
NOTICE FOR INTERNAL APPLICANTS
In accordance with all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separationpackage, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders (for example, a requirement to be vaccinated against COVID-19 in order to access a facility or meet with stakeholders). Please understand that, as permitted by applicable law, if you have not been vaccinated against COVID-19 and an essential function of your job is to call on external stakeholders who require vaccination to enter their premises or engage in face-to-face meetings, then your employment may pose an undue burden to business operations, in which case you may not be offered employment, or your employment could be terminated. Please also note that, where permitted by applicable law, the Company reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature of the role presents an increased risk of disease transmission.
Current Employees apply
Current Contingent Workers apply
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U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, generally Tuesday, Wednesday and either Monday or Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence. This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as \xe2\x80\x9cremote\xe2\x80\x9d.
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Employee Status: Regular
Relocation: Domestic/International
VISA Sponsorship: Yes
Travel Requirements: 25%
Flexible Work Arrangements: Remote Work, Telecommuting
Shift: Not Indicated
Valid Driving License: No
Hazardous Material(s): n/a
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