Director, Medical Portfolio Lead – Women's Health
Viatris
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇺🇸 United States
Visit company websiteSalary
💰 $112,000 - $236,000 per year
Job Level
Senior
About the role
- Medical Affairs Colleagues across Viatris are a source for credible, unbiased, and scientifically accurate clinical, Healthcare Economic Information (HCEI), and Medical Information about Viatris assets, medicines, and related disease states
- Medical Affairs Colleagues engage with a variety of external parties, including Healthcare Providers (HCPs), the Healthcare Community, independent third-party organizations, patients, payers, regulatory authorities, and policy makers
- Medical Affairs engage in non-promotional, truthful, and non-misleading ways to inform all parties on safe and effective use of Viatris medicines
- US Medical Affairs’ five primary responsibilities: Strategy & Insight Generation, Organizational Support, Stakeholder Engagement, Evidence Generation & Dissemination, Personal & Professional Development
- Recognized as an expert with knowledge of strategies that can be deployed within Medical Affairs
- The US Women’s Health (WH) Medical Portfolio Lead (MPL) is an HQ-based Medical Affairs function positioned as the scientific interface between Viatris and the external medical community
- The US WH MPL helps ensure the safe and effective use of Viatris medicines by supporting internal and external stakeholders with expertise related to the current portfolio
- Partnering internally on the development and launch of new products and indications, and generating new evidence
- This role works with HQ commercial colleagues as part of a cross functional team to develop an overarching strategy
- The US WH MPL identifies areas of unmet medical need and develops in alignment with the US Women’s Health Medical Lead Objectives, Strategies, Tactics, Metrics and Targets independent from commercial influence
- Perform job functions in accordance with all applicable Standard Operating Procedures (SOP), federal and state laws, Occupational Safety and Health Administration (OSHA) guidelines, health authority regulations, and departmental processes
- Provide US Medical review and approval of US Marketing promotional materials
- Engage in non-promotional, truthful, and non-misleading communications with KOLs
- Present findings from research or other scientific information as a publication, oral or poster presentation at Congress & Scientific Meetings
- Attend and actively participate in activities governed by promotional standards (e.g., medical congress satellite symposia, national webinars)
- Provide training to internal Viatris functions on products and disease states using materials approved by the MRC or the Viatris Promotional Material Approval Process (VMap) at the request of Commercial as appropriate
Requirements
- Minimum of 8 years of experience in the pharmaceutical, biotech or clinical (e.g., hospital setting/patient care) industry
- Advanced degree (MD, PhD, PharmD) is required
- Experience in OB/GYN is required
- Must possess knowledge of the US WH MPL roles and responsibilities, clinical trials, relevant therapeutic areas, understand all applicable Standard Operating Procedures (SOPs), the Standards for Interactions with U.S. Healthcare Providers, Federal and State promotional laws and regulations, the PhRMA Code, ACCME Standards, and the Code of Business Conduct and Ethics
- Must possess ability to effectively communicate, develop, and manage collaborative relationships with KOLs and other medical professionals, external academic institutions and Patient Advocacy Groups
- Strong analytic and organizational skills in managing, interpreting, and presenting clinical data
- Ability to actively listen for insights stated directly or indirectly by stakeholders and draw implications for Viatris
- Driven by personal accountability & high levels of performance
- Ability to set and accomplish compelling goals both individually and in a team setting
- Motivated to overcome challenges, seek out opportunities, and develop both personally and professionally
- Comfortable with change
- Embraces the principles of Diversity, Equity & Inclusion (DEI)
- Ability to read and interpret comprehensive and intricate research documents
- Ability to write scientific reports and technical correspondence
- Ability to work with executives and communicate abstract concepts
- Ability to present to a high level of the organization and groups outside of the organization
- Ability to perform computations such as percentages, ratios, and rates, as well as perform statistical analysis
- Ability to draw and interpret graphical data
- Ability to understand pharmaceutical calculations is preferred
- Ability to solve problems with a variety of concrete variables through semi-standardized solutions that require some ingenuity and analysis
- Ability to draw inferences and follow prescribed and detailed procedures to solve moderately complex problems
Benefits
- competitive salaries
- benefits
- an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trialsdata analysisstatistical analysispharmaceutical calculationsscientific report writingpresentation skillsevidence generationhealthcare economic informationmedical reviewSOP compliance
Soft skills
effective communicationcollaborative relationship managementanalytical skillsorganizational skillsactive listeningpersonal accountabilitygoal settingmotivationadaptabilityproblem-solving
Certifications
MDPhDPharmD