About this opportunity
Psychedelic Alpha lists this Director, Late Stage Clinical Development opportunity in myrtle point, Oregon. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale.
Our leadproductcandidate,lysergidetartrate(ourproprietary orally disintegrating tablet form oflysergide(LSD) D-tartrate),represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges.
Guided bythe recognitionthat patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to addresstheunderlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX.
Together we are moving psychiatry forward-beyond better, into a boundless future. Join us!
The Director, Late-Stage Clinical Strategy will be responsible for theend-to-end strategy development, design, and execution of Expanded Access Programs and Late-Stage studies across Definium's portfolio. This leader will provide support to ensure programs are scientifically sound, operationally feasible, regulator-ready, and aligned with the integrated asset strategy, including lifecycle management, real-world evidence generation, and post-approval commitments.
This role requires both strategic leadership and hands-on execution , with the ability to operate effectively in a lean, fast‑moving organization.
Responsibilities
Strategic Leadership
Lead aspects of the global strategy for Expanded Access Programs and Late- Stage development , aligned with asset lifecycle objectives, patient access goals, and regulatory expectations
Partner with the Executive Director Late-Stage Clinical Strategy, Clinical Development, Clinical Operations, HEOR, Medical Affairs, Regulatory Affairs, Commercial, Asset Strategy Lead and Program Leadership to ensure Expanded Access Program and Late-Stage clinical activities are fully integrated into the overall asset strategy
Expanded Access Program Execution
Lead the development and implementation of Expanded Access Programs, including protocol development, eligibility criteria, safety oversight, and operational execution
Collaborate with cross-functional planning team to ensure Expanded Access Programs are compliant, scalable, ethically sound, and aligned with regulatory guidance
Provide consultation to benefit-risk assessment, safety monitoring, and ongoing program evaluation
Late-Stage Strategy & Execution
Support the development of the late-stage clinical evidence generation strategy objectives, including real-world evidence generation, long-term safety, effectiveness, and differentiation in the treatment landscape
Lead the design, planning, and execution of the late-stage clinical evidence program, including protocol development, data collection strategies, and interpretation of outcomes for Phase 4 and investigator-initiated trials.
Ensure late-stage clinical program designs address regulatory commitments, payer needs, and scientific gaps
Regulatory & Scientific Leadership
Collaborate in the preparation and review of clinical content for regulatory submissions and interactions as applicable
Provide clinical input into Investigator Brochures, clinical study reports, in collaboration with Regulatory Affairs
Cross-Functional & External Engagement
Work collaboratively with Clinical Operations, Clinical Development, Data Management, Biostatistics, Pharmacovigilance, and Project Management to ensure high-quality execution
Establish and maintain relationships with key investigators, advisors, and external experts to support EAP and late stage/potentially Phase 4 objectives
Provide clinical leadership within matrix teams, modeling accountability, collaboration, and scientific rigor
Qualifications
Education & Experience
Doctoral degree required (MD, PhD, PharmD, PsyD)
6-8+ years of clinical development experience in the pharmaceutical or biotechnology industry
Demonstrated experience leading Expanded Access programs and late-stage, post-approval programs
Experience selecting and managing third-party vendors to support operational functions of Expanded Access and late-stage evidence programs
CNS clinical development experience in psychiatry strongly preferred
Experience with budget ownership to include forecasting tracking, and managing across multiple programs
Skills & Competencies
Working knowledge of expanded access program requirements, clinical development, regulatory pathways, and lifecycle management
Proven ability to translate strategy into execution in resource-constrained environments
Track record of effective cross-functional leadership and external stakeholder engagement
Ability to operate with diplomacy, influence without authority, and command credibility with senior leaders and external experts
Excellent verbal and written communication skills
Self-motivated, adaptable, and comfortable balancing strategic thinking with hands-on contribution
Mindset & Fit
Comfortable rolling up sleeves while maintaining a strategic perspective
Energized by innovation in clinical research and patient‑centric access models
Thrives in a fast‑paced, evolving environment with high accountability
Acts as a role model for scientific excellence, integrity, and collaboration
The starting base pay range for this position is $215,000.00 - $250,000.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location.
Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including:
100% paid health benefits including Medical, Dental and Vision for you and your dependents
401(k) program with company match and vesting after the turn of the first month after your start date
Flexible time off
Generous parental leave and some fun fringe perks!
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Worksite address
myrtle point, OR, 97458, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.