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HEOR Consultant
1 week ago
Clinical Resource Network (CRN) Princeton, United StatesOur client is looking to fill the role of HEOR Consultant. This position will be fully remote. This position serves as the lead for HTA launch readiness projects for Nephrology products. Supports under the Director, Health Outcomes this individual will develop elements of a dossi ...
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HEOR Consultant
1 day ago
Clinical Resource Network (CRN) Princeton, United StatesOur client is looking to fill the role of HEOR Consultant. This position will be fully remote. This position serves as the lead for HTA launch readiness projects for Nephrology products. Supports under the Director, Health Outcomes this individual will develop elements of a dossi ...
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Lead Data Scientist
1 week ago
Novo Nordisk Princeton, United States**About the Department*** · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA ...
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Associate Director
6 days ago
Novo Nordisk Plainsboro, United States**About the Department** · *** · Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive to deliver the best possible outcomes for p ...
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Sun Pharmaceuticals, Inc Princeton, United States**(ONSITE-Princeton) HYBRID: 3 days in office; 2 days remote** · **Summary** · Suns rapidly growing portfolio in dermatology, ophthalmology and oncology requires expansion of the market access team to globally support key Health technology assessment markets (UK, France, Germany, ...
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Sun Pharmaceutical Industries Princeton, United States(ONSITE-Princeton) HYBRID: 3 days in office; 2 days remote · Summary · Sun's rapidly growing portfolio in dermatology, ophthalmology and oncology requires expansion of the market access team to globally support key Health technology assessment markets (UK, France, Germany, Canada ...
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director, medical affairs
1 week ago
Sun Pharmaceutical Industries Princeton, NJ, United StatesCOME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE · * Hybrid work arrangement · * Medical, Dental, Vision Benefits · * Health Savings Account (HSA), Flexible Spending Account (FSA) · * Prescription Drug Coverage · * Telehealth and Behavior Health Services · * Income Pr ...
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GENMAB A/S Princeton, United StatesAt Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, ca ...
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Moderna Theraputics Princeton, NJ, United StatesThe Role: · Moderna is seeking a Director of Epidemiology, Early HEOR & Patient-Centered Outcomes Assessment (Epi, & PCOA) to support the strategy, design and implementation of evidence generation activities activities targeted towards supporting the regulatory approval and reim ...
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Director, Medical Affairs
1 week ago
Sun Pharmaceutical Industries Princeton, United StatesCOME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEEHybrid work arrangementMedical, Dental, Vision BenefitsHealth Savings Account (HSA), Flexible Spending Account (FSA) Prescription Drug CoverageTelehealth and Behavior Health ServicesIncome Protection Short Term and Long ...
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Senior Director Medical Affairs
1 week ago
ACADIA Pharmaceuticals Inc. Princeton, United StatesPlease note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. · The Senior Medical Director will lead the development and execution of the medical strategy for Rett Syndrome. This will be a ...
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Lead Data Scientist
23 hours ago
Novo Nordisk Princeton, United States Full timeAbout the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...
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Remote-Medical Director
4 days ago
Novo Nordisk Plainsboro, United States Full timeAbout the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to p ...
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Remote-Medical Director
1 week ago
BioSpace Plainsboro, United StatesJob Details · About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies wi ...
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Medical Director
1 week ago
BioSpace Plainsboro, United StatesJob Details · About the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies wi ...
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Medical Director
1 week ago
Novo Nordisk Plainsboro, United States Full timeAbout the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to p ...
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Associate Director
2 weeks ago
Novo Nordisk Plainsboro, United States Full timeAbout the Department · At Novo Nordisk, our Finance and Operations team is the engine that elevates holistic commercialization of our products. The Finance and Operations team works closely with the business across the organization to guide enterprise wide resource allocations, ...
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Novo Nordisk Plainsboro, United StatesAbout the Department · Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive to deliver the best possible outcomes for patients wi ...
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Senior Director
2 days ago
Novo Nordisk Plainsboro, United StatesAbout the Department · Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. We strive to deliver the best possible outcomes for patients wi ...
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Remote-Medical Director
4 days ago
Novo Nordisk Plainsboro, United States Full timeAbout the Department · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to ...
HEOR Consultant - Princeton, United States - GForce Life Sciences
Description
The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in delivering on the evidence strategy across the product life cycle for payer/HTA needs.
Role Description:
The VRWE Scientist supports the development and execution of a comprehensive, and scientifically rigorous global value dossier (ie, systematic lit reviews, HE models, RWE, observational studies), including but not limited to:
High-quality health economics and payer evidence input into pharmaceutical development projects, payer evidence strategy and plans
Participate in external health economics and payer evidence departmental activities via technical presentations, publication development, and other similar activities
This role is part of a global cross-functional team and interacts with Global Clinical Development, Clinical Management, Regulatory Affairs, Biostatistics, Global Medical Affairs, Commercial, Market Access, Government Affairs, and other colleagues to stay abreast of clinical development program needs for value differentiation in alignment with the target product profile across the product lifecycle.
Job Responsibilities:
High-quality health economics and payer evidence input into pharmaceutical development projects, and payer evidence plans
Deliver clear, customer-focused and robust Global Reimbursement Dossiers (GRDs)
Advocate and champion the need for scientifically sound trial and non-trial data (including RWE, economic modeling, meta-analyses, observational studies, and PRO approaches
Manage relationships with vendors to ensure timely completion of high-quality projects
Communicate study plans, study methods, and results to internal teams
Present research findings at scientific congresses and/or via manuscripts
Ensure compliance with all applicable laws, regulations, and regulatory guidelines
Maintain awareness, education on and implementation of HEOR methods (qualitative, quantitative, interventional, and non-interventional), tools, and data sources to ensure study methods represent current state of science, as well as assessment and interpretation of relevant literature, scientific dissemination in line with internal communication
Manage budget resources allocated to assigned projects
Travel (approximately 15%)
Willingness to travel to conferences, various corporate locations, and stakeholder meetings, including overnight trips.
Required Qualifications:
Graduate degree in biomedical science, business, quantitative disciplines or economics (outcomes research, health services research, epidemiology, public health, community health, or related fields).
Formal post-graduate degree (or equivalent applied work) in health economics or a related quantitative discipline, and work experience in the discipline.
At least 5+ years of professional experience in evidence generation in a Pharmaceutical or consulting role
Excellent knowledge of clinical development and research study designs and interpretation
Good understanding of qualitative and quantitative approaches
Comprehensive understanding of the pharmaceutical industry and regulatory requirements from a global perspective and product development processes at all life cycle stages.
Knowledge of international healthcare systems and their changing needs for HTA submission
Able to implement projects including interactions with key stakeholders with a high degree of autonomy
Ability to work independently, deal with complex issues, and relate to multiple internal and external stakeholders.
Good communication skills as it relates to engagement of both internal (upper management) and external (key stakeholder); ability to work from both a business and interpersonal perspective with colleagues within the organization across multiple departments.
Excellent written and verbal communication skills, negotiation, collaboration, and interpersonal skills
Highly motivated self-starter who is able to work independently, deal with complex issues and relate to multiple internal and external stakeholders.
Experience working with and overseeing external contractors and vendors.
Project Management experience
Terms:
12+ month contract
Remote, must work EST
Travel (approximately 15%)
Willingness to travel to conferences, various corporate locations, and stakeholder meetings, including overnight trips.
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