Oncology Regional Medical Scientific Director (Breast) - New England & Eastern NY

Job Description Role Summary:

The Oncology Regional Medical Scientific Director is a credentialed (i.e., PhD, Pharm

D, DNP , MD

) therapeutic and disease expert in breast cancer who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Director liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies. The Regional Medical Scientific Director serves as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.

Location :

+ This position covers Eastern NY (excludes NYC ) & New England + Must reside in geographic area with a preference for the Boston, MA area. + Up to 50% travel required with some overnight

Responsibilities and Primary Activities Scientific Exchange:

+ Develops professional relationships and engages with national and regional SLs to ensure access to medical and scientific information on areas of therapeutic interest and Company products. + Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the company. + Addresses scientific questions and directs SL inquiries on issues outside of Regional Medical Scientific Director scope (e.g., grants) to appropriate company resources consistent with applicable policies. + Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest ( AOI )

Research:

+ Upon request from Global Center for Scientific Affairs ( GCSA ), initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial. + Enhances the comprehension of the scientific foundations and goals of investigator-sponsored research. + Identifies barriers to patient enrollment and retention efforts to achieve study milestones. + Upon request from Global Clinical Trial Operations ( GCTO ), + Recommends study sites and identifies potential investigators to participate in phase II- III clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. + Addresses questions from investigators and provides information regarding participation in company-sponsored clinical studies

Scientific Congress Support:

+ Engages in scientific congresses and medical meetings, facilitates scientific and data exchange for both internal and competitor data.

Scientific Insights:

+ Gathers feedback, data, or information during routine activities that can help the company better comprehend medical or scientific needs, priorities, or concerns of SLs and/or patients

Required Qualifications, Skills, & Experience Minimum:

+ PhD, PharmD, DNP , or MD. + Proven competence and a minimum of 3 years of oncology experience beyond that obtained in the terminal degree program, with strong preference for experience in Breast Oncology Malignancies. + Ability to conduct doctoral-level discussions with key external stakeholders. + Dedication to scientific excellence with a strong focus on scientific education and dialogue. + Excellent stakeholder management, communication, and networking skills. + A thorough comprehension of

FDA , OIG , HIPAA

, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. + Ability to organize, prioritize, and work effectively in a constantly changing environment. + Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel, Access) Desire to contribute to an environment of belonging, engagement, equity, and empowerment by: + Working to transform the environment, culture, and business landscape. + Leveraging competitive advantage, per global strategy. + Ensuring accountability to drive an inclusive culture. + Strengthening the foundational elements. + Consistent adherence to field and corporate policies and Global Medical Scientific Affairs ( GMSA ) strategy, including field standard operating procedures (SOPs), Good Clinical Practice ( GCP ) guidelines, and administrative/operational responsibilities

Preferred:

+ Field-based medical affairs experience + Experience in Breast Oncology Malignancies + Experience in immuno-oncology and antibody drug conjugates + Research experience + Demonstrated record of scientific/medical publication \#eligiblefor

ERP Required Skills:

Breast Cancer, Breast Oncology, Clinical Oncology, Medical Affairs, Medical Knowledge, Pharmaceutical Medical Affairs, Professional Networking, Scientific Research, Strategic Thinking Preferred Skills:

Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088\ EEOC \ KnowYourRights\ 10\ 20.pdf)

EEOC GINA

Supplement? We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/ CCPA -notice/) The salary range for this role is $210,400.00 - $331,100.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision heal To view full details and how to apply, please login or create a Job Seeker account