2 Medical Affairs Director - Oncology/Pathology - Remote | WFH Jobs in Carlsbad, CA
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Medical Affairs Director - Oncology/Pathology - Remote | WFH
$230k-290k (estimate)
Full Time
2 Weeks Ago
Get It Recruit - Healthcare is Hiring a Remote Medical Affairs Director - Oncology/Pathology - Remote | WFH
Position OverviewAs part of our team, you'll engage in meaningful work that has a positive impact globally. Join over 120,000 colleagues dedicated to making the world healthier, cleaner, and safer. You'll have the resources to achieve your career goals and contribute to solutions for some of the world's toughest challenges, including environmental protection, food safety, and cancer cures.
Role SummaryThe Director of Medical Affairs will play a pivotal role in strategically and functionally leading the North American Medical Affairs Team. This position supports the Clinical Sequencing Division (CSD) initiatives, which are at the forefront of Precision Medicine and widely adopted by major healthcare providers. The goal is to extend clinical reach through supporting clinical validity/utility studies and generating real-world data (RWD) locally. The Director will formulate a strategy specifically tailored for North America to bolster growth in pathology and oncology. This role also involves fostering collaborations with pharmaceutical partners and spearheading peer-to-peer medical educational initiatives.
Key ResponsibilitiesDevelop and provide training materials for Medical Science Liaisons (MSLs), establish a robust KPI system, and build essential field medical affairs infrastructure.
Lead the expansion of the medical affairs field team to support assays in both pre-launch and post-launch phases.
Build strong relationships with cross-functional business unit team members.
Maintain and enhance high-level engagement with Key Opinion Leaders (KOLs) to develop impactful research and access strategies.
Strategize for evidence generation in pathology and oncology using Next-Generation Sequencing (NGS), focusing on Clinical Validity/Utility studies.
Facilitate and support investigator-sponsored trials/studies, ensuring efficient execution and reporting.
Develop and deliver core training across teams, focusing on product launch readiness and scientific and medical knowledge consistency.
Educate internal teams about disease state changes, competitive intelligence, and KOL insights relevant to our products.
Collaborate with the Global Medical Affairs Leader on medical education strategy and implementation.
Optimize delivery of medical and scientific services to both internal and external partners.
Provide medical and clinical expertise to a broad range of stakeholders.
Stay updated with clinical literature in NGS, especially in pathology and oncology.
Translate Medical Affairs resources into valuable materials for internal stakeholders.
Work closely with sales and marketing directors for optimal alignment of field resources and successful product launches.
Minimum Requirements/QualificationsAdvanced degree (MD, MD/PhD, or PhD).
5 years of experience in Medical Affairs within pharmaceuticals, medical devices, or diagnostics.
Background in clinical diagnostics, pathology/genetics laboratory, and oncology preferred.
Strong negotiation, problem-solving, and strategic influencing skills.
Ability to articulate complex scientific data to diverse audiences.
Proven ability to meet tight deadlines and adapt to changing priorities.
Understanding of market access dynamics and the role of clinical evidence in access decisions.
Experience in delivering clinical evidence, dossier adaptations, and scientific publications.
Knowledge of Clinical Development SOPs and CAP-CLIA/NCCN guidelines is highly desirable.
International experience and cultural awareness is a plus.
Willingness to travel at least 35% of the time.
Ability to work remotely in North America but must be available for periodic travel to the San Francisco or San Diego offices.
Why Join Us?
Our mission is to enable our customers to make the world healthier, cleaner, and safer. Join a team of over 100,000 colleagues who share values of integrity, intensity, innovation, and involvement. We accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.
Compensation And BenefitsWe offer competitive remuneration, an annual incentive plan bonus, and a comprehensive benefits package, including:
A choice of national medical, dental, and vision plans, including health incentive programs.
Employee assistance and family support programs, commuter benefits, and tuition reimbursement.
Paid time off (PTO), paid holidays, paid parental leave, accident and life insurance, and short- and long-term disability.
Retirement and savings programs, including a 401(k) plan and an Employee Stock Purchase Plan (ESPP).
Apply Today!
Join our innovative and forward-thinking organization that offers outstanding career and development prospects. We embrace diversity, valuing diverse experiences, backgrounds, and perspectives. Apply now to start your journey with us.
We are an Equal Employment Opportunity (EEO)/Affirmative Action Employer and do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
Employment Type: Full-Time
Role SummaryThe Director of Medical Affairs will play a pivotal role in strategically and functionally leading the North American Medical Affairs Team. This position supports the Clinical Sequencing Division (CSD) initiatives, which are at the forefront of Precision Medicine and widely adopted by major healthcare providers. The goal is to extend clinical reach through supporting clinical validity/utility studies and generating real-world data (RWD) locally. The Director will formulate a strategy specifically tailored for North America to bolster growth in pathology and oncology. This role also involves fostering collaborations with pharmaceutical partners and spearheading peer-to-peer medical educational initiatives.
Key ResponsibilitiesDevelop and provide training materials for Medical Science Liaisons (MSLs), establish a robust KPI system, and build essential field medical affairs infrastructure.
Lead the expansion of the medical affairs field team to support assays in both pre-launch and post-launch phases.
Build strong relationships with cross-functional business unit team members.
Maintain and enhance high-level engagement with Key Opinion Leaders (KOLs) to develop impactful research and access strategies.
Strategize for evidence generation in pathology and oncology using Next-Generation Sequencing (NGS), focusing on Clinical Validity/Utility studies.
Facilitate and support investigator-sponsored trials/studies, ensuring efficient execution and reporting.
Develop and deliver core training across teams, focusing on product launch readiness and scientific and medical knowledge consistency.
Educate internal teams about disease state changes, competitive intelligence, and KOL insights relevant to our products.
Collaborate with the Global Medical Affairs Leader on medical education strategy and implementation.
Optimize delivery of medical and scientific services to both internal and external partners.
Provide medical and clinical expertise to a broad range of stakeholders.
Stay updated with clinical literature in NGS, especially in pathology and oncology.
Translate Medical Affairs resources into valuable materials for internal stakeholders.
Work closely with sales and marketing directors for optimal alignment of field resources and successful product launches.
Minimum Requirements/QualificationsAdvanced degree (MD, MD/PhD, or PhD).
5 years of experience in Medical Affairs within pharmaceuticals, medical devices, or diagnostics.
Background in clinical diagnostics, pathology/genetics laboratory, and oncology preferred.
Strong negotiation, problem-solving, and strategic influencing skills.
Ability to articulate complex scientific data to diverse audiences.
Proven ability to meet tight deadlines and adapt to changing priorities.
Understanding of market access dynamics and the role of clinical evidence in access decisions.
Experience in delivering clinical evidence, dossier adaptations, and scientific publications.
Knowledge of Clinical Development SOPs and CAP-CLIA/NCCN guidelines is highly desirable.
International experience and cultural awareness is a plus.
Willingness to travel at least 35% of the time.
Ability to work remotely in North America but must be available for periodic travel to the San Francisco or San Diego offices.
Why Join Us?
Our mission is to enable our customers to make the world healthier, cleaner, and safer. Join a team of over 100,000 colleagues who share values of integrity, intensity, innovation, and involvement. We accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need.
Compensation And BenefitsWe offer competitive remuneration, an annual incentive plan bonus, and a comprehensive benefits package, including:
A choice of national medical, dental, and vision plans, including health incentive programs.
Employee assistance and family support programs, commuter benefits, and tuition reimbursement.
Paid time off (PTO), paid holidays, paid parental leave, accident and life insurance, and short- and long-term disability.
Retirement and savings programs, including a 401(k) plan and an Employee Stock Purchase Plan (ESPP).
Apply Today!
Join our innovative and forward-thinking organization that offers outstanding career and development prospects. We embrace diversity, valuing diverse experiences, backgrounds, and perspectives. Apply now to start your journey with us.
We are an Equal Employment Opportunity (EEO)/Affirmative Action Employer and do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
Employment Type: Full-Time
Job Summary
JOB TYPE
Full Time
SALARY
$230k-290k (estimate)
POST DATE
06/09/2024
EXPIRATION DATE
07/07/2024
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