Director, HEOR - $10,000.00 Sign-on bonus!
Cancer Treatment Centers of America® (CTCA®) takes a unique and integrative approach to cancer care. Our patient-centered care model is founded on a commitment to personalized medicine, tailoring a combination of treatments to the needs of each individual patient. At the same time, we support patients’ quality of life by offering therapies designed to help them manage the side effects of treatment, addressing their physical, spiritual and emotional needs, so they are better able to stay on their treatment regimens and get back to life. At the core of our whole-person approach is what we call the Mother Standard® of care, so named because it requires that we treat our patients, and one another, like we would want our loved ones to be treated. This innovative approach has earned our hospitals a Best Place to Work distinction and numerous accreditations. Each of us has a stake in the successful outcomes of every patient we treat. Job Description:
Cancer care is all we do
Hope in healing
***This position comes with a $10,000.00 sign-on bonus!***
Vidence harnesses the power of clinical and genomic data and insights to advance the treatment and outcomes for oncology patients. A healthcare informatics company, Vidence provides the world’s leading cancer researchers, innovators and treatment providers with the ability to contribute to and access the most comprehensive knowledge base of patient journeys and outcomes. Vidence Consortium Fellows are leading healthcare systems, independent hospitals, and cancer clinics that leverage the clinical and research tools of the Vidence technology platform, Scimon. Scimon includes information and insights on more than 100,0000 patients from electronic health records (EHR), genomic testing results, patient surveys, claims and other key data points. Utilizing advanced technology including natural language processing (NLP), machine learning (ML), artificial intelligence (AI) and a comprehensive suite of professional services, Vidence provides data visualization, insights, and data analytics to Consortium Fellows and others in the medical community to support quality improvement, precision medicine and clinical advancement.
This role will be an integral part of a cross functional team to deliver HEOR/RWE projects for internal and external stakeholders. The Director will design, develop, and deliver HEOR projects, in addition to working with external clients to ensure all projects are successfully delivered. The Director is responsible for quality control on all work distributed internally and externally.
Design, develop, and deliver funded research projects, primarily in MS Word, using research knowledge around literature review, study design, statistical analyses, hypothesis development, plans for results and report lay-out, critically analyze conclusions and identify opportunities for dissemination including but not limited to professional conference presentation and peer-reviewed journal publication.
Work closely with functional partners across the business to ensure project delivery success
Interact with internal and external project team members
Ensure the HEOR team’s strategic plan is aligned with company priorities
Develop HEOR team strategic plans and contribute to the growth of the HEOR group through internal and external initiatives
Ensure all deliverables, including proposals, statistical analysis plans, results, final reports and publications meet the highest level of scientific quality standards
Ensure timely delivery of the projects in collaboration with other cross-functional team members
Participate in client discussions at all phases of the study lifecycle from study concept, design and methods considerations, analysis progress, results presentations, etc.
At least 3+ years of relevant HEOR pharmaceutical industry, CRO, or academic experience with consulting experience.
Bachelor’s degree required, related field preferred.
Graduate degree (PharmD, MS, MPH, PhD) in Economics, Health Economics, Outcomes research (Pharma) epidemiology, or related field preferred. Must possess strong research design and analysis skills, including scientific methods experience, significant understanding of study design and statistical analyses
Must have strong writing skills and be able to manage multiple studies simultaneously
Knowledge of oncology data and systems is required
Must have ability to visually display study results (a high level of understanding of graphic display in MS PowerPoint, Excel, and Word)
This is a leadership role with future direct reports TBD.
Each CTCA employee is a Stakeholder, driven to make a true difference and help win the fight against cancer. Each day is a challenge, but this unique experience comes with rewards that you may never have thought possible. To ensure each team member brings his or her best self, we offer exceptional support and immersive training to encourage your personal and professional growth. If you’re ready to be part of something bigger and work with a passionate, dynamic group of care professionals, we invite you to join us. Visit: Jobs.cancercenter.com to begin your journey.
We win together
Visit: Jobs.cancercenter.com to begin your journey.
Job Status: Full Time
Job Reference #: JR-05613