Support the value evidence team in GI cancers and contribute to value evidence strategies for in-line and pipeline products, serving as an outcomes research representative on cross-functional teams.
Compensation
The salary range for the primary location of this role is: $156,900.00 - $247,000.00
Responsibilities
Support the value evidence team in GI cancers and contribute to value evidence strategies for in-line and pipeline products.
Serve as outcomes research representative on cross-functional regional and global teams.
Critically assess drivers and barriers to reimbursement and market access, and provide input into clinical, regulatory, payer/access, marketing and evidence generation strategies and programs.
In collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications.
Responsible for study-related contracting, budgets, and vendor/partner management.
Experienced Evidence Generation Manager with deep expertise in Real World Evidence (RWE) to develop and deliver high-quality evidence that demonstrates the value of medicines, informs product strategy, and supports patient access for patients.
Responsibilities
Develop, evaluate and deliver high-quality RWE and evidence-generation strategies aligned with product, medical and market access objectives.
Identify evidence gaps and opportunities, using Real World Data to understand unmet needs and inform strategic priorities.
Lead RWE and other evidence projects from research hypothesis and study design through execution, analysis, publication and communication.
Manage collaborations with academic institutions, research partners and CROs, ensuring projects are delivered to agreed timelines, budgets and quality standards.
Contribute evidence and scientific expertise to value demonstration plans, reimbursement and formulary submissions, HTA activities and regulatory discussions.
Requirements
Master’s degree in Biomedical Science, Medical Science or a related discipline
MD or equivalent advanced scientific qualification (preferred)
Lead scientific and strategic evidence generation for Balkan region at AstraZeneca.
Responsibilities
Develop, evaluate and deliver high-quality RWE and evidence-generation strategies aligned with product, medical and market access objectives.
Identify evidence gaps and opportunities using Real World Data.
Lead RWE and other evidence projects from hypothesis to execution, analysis, publication and communication.
Manage collaborations with academic institutions, research partners and CROs.
Contribute evidence and scientific expertise to value demonstration plans, reimbursement and formulary submissions, HTA activities and regulatory discussions.
Requirements
Master’s degree in Biomedical Science, Medical Science or a related discipline
MD or equivalent advanced scientific qualification
Lead the design, development, and maintenance of scalable data pipelines and semantic data engineering frameworks for real‑world evidence studies, dashboards, and AI‑ready datasets.
Responsibilities
Develop automated data processes for patient‑level data generation
Transform heterogeneous raw healthcare datasets into reusable data models
Build FAIR data pipelines and semantic frameworks
Create AI‑ready datasets for generative AI use cases
Engage technically with stakeholders to translate requirements into data structures
Requirements
Nice to have: R programming
Nice to have: sparklyR
Nice to have: R Shiny
Nice to have: Observational research methodologies
The Associate Director is responsible for cultivating and growing Tempus partnerships with pharmaceutical and biotechnology clients to support them in advancing their research, clinical and/or commercial programs.
Locations (4)
Illinois, United States
California, United States
Colorado, United States
New York, United States
Compensation
$90,000-$150,000. The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications.
Responsibilities
Identify high potential customer contacts at biopharma companies based on alignment with Tempus offerings and commercial strategy
Principal Scientist (Director) - Outcomes Research - Lung Cancers
Doctoral degree (PhD, DrPH, ScD, PharmD) in health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration
Masters degree (MSc, MPH) in health services research, outcomes research, epidemiology, public health, health economics, pharmacoeconomics, pharmacy administration
Conduct outreach to executives at life sciences companies to open partnering discussions
Identify customer needs and effectively communicate the value proposition of Tempus product lines
Support development of global account strategy in coordination with Data & AI Partnerships Directors, scientific teams and business operations teams
Contribute to meeting and exceeding revenue goals across Tempus product lines at accounts while supporting delivering on established strategic objectives for specific client accounts
Requirements
Bachelor or advanced degree in a Science or Business discipline
Nice to have: 2+ years working with companies who serviced Life Sciences companies in research and development, real world data or molecular diagnostics
Advanced or professional degree in a relevant discipline (e.g., Outcomes Research, Health Economics, Epidemiology, Pharmaceutical Administration, Public Health, Health Policy, Medicine, or Clinical Pharmacy)
Associate Director, Outcomes Research (Oncology)Merck · Rahway, US
Balkan Evidence Generation ManagerAstraZeneca · Belgrade, Serbia