
1001 - 5000 employees
Founded 2007
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Tolmar is a specialty pharmaceutical company that develops, manufactures, and commercializes long-acting injectable medicines primarily for urology, oncology, and endocrinology. The company focuses on research and development to improve patient experiences and meet unmet medical needs, operates manufacturing facilities (notably in Colorado) to supply products globally, and emphasizes patient access, education, and partnerships to bring therapies to market.
🔥 34 minutes ago
⛰️ Colorado – Remote
💵 $300k - $325k / year
⏰ Full Time
🟠 Senior
👔 Director
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Tolmar's careers page, not through a job board
First seen by Remote Rocketship 34 minutes ago
Still open on Tolmar's site. Checked 13 minutes ago.

1001 - 5000 employees
Founded 2007
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Tolmar is a specialty pharmaceutical company that develops, manufactures, and commercializes long-acting injectable medicines primarily for urology, oncology, and endocrinology. The company focuses on research and development to improve patient experiences and meet unmet medical needs, operates manufacturing facilities (notably in Colorado) to supply products globally, and emphasizes patient access, education, and partnerships to bring therapies to market.
• Develop and execute outcomes research strategies across the oncology portfolio, including solid tumors and hematologic malignancies • Lead oncology-specific HEOR strategy across pipeline and in-line therapies • Generate real-world evidence and health economic data supporting product value, regulatory strategy, and market access • Build and own Integrated Evidence Plans for Phase 3 products and commercial or business development assets • Conduct evidence gap assessments and prioritize a sequenced, budgeted study portfolio • Design and lead retrospective and prospective real-world evidence studies • Evaluate and contract oncology EHR, claims, specialty pharmacy, hub, laboratory, and linked data sources • Develop protocols and statistical analysis plans using propensity scores, target trial emulation, and external control arms where appropriate • Lead patient-centered outcomes, treatment burden, preference, and quality-of-life research • Direct US budget impact and cost-effectiveness models for payer, employer, IDN, oncology practice, and pathway audiences • Own AMCP dossiers and pre-approval information exchange materials • Prepare for ICER assessments and support compendia, NCCN, and pathway submissions • Develop payer and HTA-ready oncology value narratives and tools • Own the HEOR/RWE publication plan, including abstracts, posters, and manuscripts • Serve as Tolmar’s scientific voice with payers, HTA bodies, KOLs, and data partners • Build the HEOR/RWE function, including operating model, SOPs, governance, and review processes • Recruit, lead, and develop a team over the next 18–36 months • Select and manage consultancies, real-world data providers, and CROs • Own the evidence budget and deliver studies on time and on budget • Ensure compliance with FDA, OIG, PhRMA Code, HIPAA, privacy, and data-use requirements • Partner with Clinical Development, Medical Affairs, Market Access, Commercial, Pricing, Regulatory, and academic stakeholders
• Advanced degree required (PhD, MD, MPH) in relevant scientific discipline • 12+ years of experience in HEOR, Market Access, or Medical Affairs within the pharmaceutical/biotech industry • Demonstrated expertise in epidemiology and biostatistics related to design and analysis • Familiarity with relevant datasets in the US and abroad, including dataset-specific analysis considerations • Deep expertise in oncology outcomes research methodologies, clinical endpoints, and real-world evidence generation • Advanced knowledge of HEOR study design, observational research, comparative effectiveness research, epidemiology, patient-reported outcomes, and oncology health economic modeling • Understanding of oncology treatment landscapes, standards of care, and competitive dynamics • Experience developing integrated evidence generation plans • Understanding of payer, health technology assessment, and reimbursement requirements • Experience evaluating claims, electronic health records, registries, chart reviews, and oncology-specific datasets • Knowledge of regulatory, legal, privacy, publication, and compliance requirements • Strong project management, prioritization, leadership, coaching, and talent development skills • Oncology experience strongly preferred • Experience with physician-administered, buy-and-bill products and Part B/commercial medical benefit economics preferred • Experience building a function in a smaller or growing company preferred • Exposure to ICER assessments, NCCN or pathway submissions, and IDN/oncology practice value discussions preferred • Patient-reported outcomes and preference research experience preferred • Experience supporting portfolio or business development evaluations preferred • Ability to travel up to 30%
• Bonus eligible • Benefits package • Equitable, fair pay practices • Travel up to 30%
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