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Definium Therapeutics
Definium Therapeutics
16 open remote positions
Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Founded in 2019, they are continuously expanding their presence and global footprint, searching for high-impact individuals.
Salary Distribution
16 of 16 jobs
Benefits Overview
16 of 16 jobs
401(k)
(16)
Dental
(16)
Medical
(16)
Vision
(16)
PTO
(14)
Equity
(9)
Parental leave
(8)
Bonus
(7)
Parental Leave
(6)
Flexible Time Off
(2)
Fringe Perks
(1)
Open Positions
Serve as a clinical science representative on global development teams. Provide therapy‑area medical and scientific expertise in the evaluation and presentation of clinical trial data. Contribute to a culture of innovation, collaboration, and continuous improvement.
Clinical Development
Data Analysis
Cross-functional Collaboration
Recruit, onboard, train, and develop MSL talent to build a culture of excellence and accountability. Oversee regional KOL mapping, segmentation, and engagement plans aligned with national medical strategy. Guide regional execution of scientific engagement at national and regional psychiatry conferences, advisory boards, and educational events.
Psychiatry
Medical Affairs
KOL Engagement
Provide legal counsel to Sales, Marketing, Medical Affairs, advising on regulatory matters. Participate in MLR Review Committees and advise on advertising and scientific exchange. Ensure compliance with laws, regulations, policies, procedures, and controls.
FDA
Legal Counsel
Pharmaceutical
Compliance
Contract Drafting
Prepare and post monthly journal entries in accordance with GAAP Process and enter vendor invoices in Coupa, ensuring accuracy and compliance Reconcile corporate credit card transactions and ensure proper documentation
Accounting
Finance
Coupa
NetSuite
SOX
Serve as Study Biostatistician for assigned clinical trials to provide statistical support from design, analysis to reporting Collaborate with cross-functional experts on clinical trial designs and make contributions to determination of objectives, endpoints and sample size Conduct data analyses as needed by using own SAS programs in collaboration with internal Statistical Programming team
SAS
Biostatistics
Data Analysis
Provide statistical programming leadership to support analysis and reporting for assigned clinical programs. Lead a group of Statistical Programmers to deliver while also being hands-on. Work closely with biostatisticians for data analysis, vendor supervision and provide programming leadership to support Definium’s integrated data analyses.
SAS
SDTM
ADaM
CDISC
Biostatistics
Develop and maintain end-to-end global supply chain strategy and supply network from drug substance through to finished drug product. Oversee management of commercial contract manufacturers suppliers and identify opportunities for efficiencies and cost reduction. Develop risk mitigation strategies which enable uninterrupted supply & business continuity.
Supply Chain
Pharmaceutical
Manufacturing
Inventory Management
Prepare and review month‑end accruals related to clinical trials, CROs, sites, and other R&D vendors. Validate monthly site payments and partner with the Company’s site payment vendor to resolve discrepancies. Perform detailed monthly actual‑versus‑budget variance analysis for R&D and Clinical Operations spend.
Accounting
Finance
Excel
Analytical
Problem-solving
Lead and develop a high-performing national team of Account Directors. Serve as senior relationship owner for a national portfolio of key payer stakeholders. Drive formulary placement, prior authorization criteria optimization, and coverage policy development.
Managed Care
Market Access
Relationship-building
Develop and lead end-to-end commercial distribution and channel strategy. Serve as the primary relationship owner for key trade vendors. Oversee trade operations including order management, inventory flow, and data reporting.
Negotiation
Develop annual marketing plans, brand strategies, and value propositions for DT120 Manage the entire product lifecycle from pre-launch to post-launch, including market assessment, segmentation, and differentiation, execution, measurement, and optimization Drive digital strategy, including Veeva systems, social media, and web initiatives to engage Healthcare Professionals (HCPs) and patients
Marketing
Brand Management
Digital Strategy
Market Analysis
Cross-functional Collaboration
Design, build, and scale patient support services infrastructure Own the end-to-end patient journey from referral through therapy initiation Establish program goals, performance benchmarks, and continuous improvement frameworks
Patient Services
Market Access
HIPAA
Compliance
Lead development and execution of pricing and contracting strategy across all commercial channels Own all government price reporting obligations including Medicaid Best Price, AMP, ASP, and 340B program compliance Implement and optimize systems and processes to ensure scalable, accurate, and auditable contracting operations
Pricing
Contracting
Market Access
Finance
Develop and maintain commercial dashboards and reporting solutions to support Sales, Marketing, and Market Access teams Translate business questions into structured analytical approaches and deliver actionable insights using claims, CRM, and other commercial datasets Build and optimize data queries (SQL) and datasets to support reporting, analytics, and ongoing business needs
Data Analytics
Business Intelligence
SQL
Tableau
Power BI
Excellent communication and interpersonal skills. Experience working in a highly matrixed organization with geographically dispersed teams. Demonstrated ability to drive initiatives, solve issues, anticipate problems and achieve objectives.
Project Management
Stakeholder Management
Microsoft Office
Microsoft Project
Responsible for the strategic oversight, operational management, and continuous improvement of the Trial Master File (TMF). Lead TMF quality review activities, including ongoing completeness checks ensuring that all required documents are accurately filed. Identify eTMF trends and commonly misfiled documents, and lead efforts to identify, communicate, and resolve document inconsistencies.
FDA