Definium Therapeutics (formerly MindMed) is a biotech company forging a new era of psychiatry by applying precision to psychedelic medicine. We develop science-led, accessible treatment approaches designed to open new routes for brain health and help people reclaim more vibrant lives. From day one, we have been powered by a radical idea: treatments for anxiety and depression should bring real relief. 

Together we’re moving psychiatry forward— beyond better, into a boundless future.

Definium Therapeutics trades on the NASDAQ under the symbol DFTX.

Industry: Biotechnology Research
Company Size: 51-200 employees

Definium Therapeutics

Savvy Admin PROD

Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.

Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.

Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.

Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.

The Senior Director, Marketing leads the development and execution of strategic marketing plans to drive the commercial launch and success of DT120, working closely with regulatory, medical, and sales teams to align with corporate goals. This role involves interpreting complex clinical data, managing brand lifecycles, and ensuring compliance with stringent regulatory standards (e.g., FDA)

**Responsibilities:**

- 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

- Oversee the promotional review process (MLR/PRC) to ensure all marketing materials, including digital and print, are compliant

- Partner with R&D, Medical Affairs, Market Access, and Sales teams to shape evidentiary needs and support commercial objectives

- Direct external advertising/media/market research agencies and manage marketing budgets to ensure high-ROI initiatives

- Drive digital strategy, including Veeva systems, social media, and web initiatives to engage Healthcare Professionals (HCPs) and patients

- Identify and build relationships with Key Opinion Leaders (KOLs) to support scientific exchange and brand positioning. Drive congress and advisory board planning and execution

**Qualifications:**

- Bachelor's degree in Life Sciences, Marketing, Business or related discipline, advance degree preferred (MBA preferred)

- Minimum 15 years in the pharmaceutical, biotech, or healthcare consulting industry, with experience in product launch and brand management

- Deep understanding of pharmaceutical regulations governing HCP and consumer promotion

- Experience with HCP and Patient/Consumer marketing required

- Proven ability to lead, mentor, and build high-performing teams, often in a matrixed environment required

- Proficiency in analyzing market trends, competitive intelligence, and financial models for forecasting

- Skilled with cross functional collaboration and astute at influence, curious to learn from others, driven to share outputs and socialize commercial strategy and objectives

- Experience with REMS product preferred

- Launch experience in the US market required

- Ability to synthesize complex data into actionable strategies

- Strong presentation skills and ability to influence senior, cross functional and sales team stakeholders

- Ability to travel as required. Average 10-20%, reaching 50% or more in some months

The starting base pay range for this position is $251,775.00 - $294,965.00 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!

Senior Director, Marketing

Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.

Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.

The Associate Director, Clinical Development plays a key role in the design and execution of ongoing and new clinical development studies. This position serves as the clinical science representative on one or more U.S. and/or global clinical studies and contributes to the delivery of high‑quality clinical data to support registration and launch. The role partners cross‑functionally with Clinical Operations, Clinical Pharmacology, Regulatory Affairs, Early Development, Medical Affairs, Commercial, and external vendors.

**Responsibilities**

- Serve as a responsible member and clinical science representative on global development teams

- Collaborate with cross‑functional partners to provide clinical development expertise in support of study execution

- Provide therapy‑area medical and scientific expertise in the evaluation and presentation of clinical trial data

- Write and edit clinical protocols, clinical study reports, manuscripts, and other study‑related documents

- Support the quality, coordination, and timeliness of clinical sections of regulatory deliverables (e.g., INDs, Investigator Brochures, CTAs, ISS/ISE, clinical expert reports) in partnership with Regulatory Affairs and Project Management

- Review and monitor patient‑level and study‑level data, including participation in blinded data review and use of data science approaches as applicable

- Collaborate with statisticians and programmers on statistical analysis plans and interpretation of clinical data

- Work with Medical Writing to support abstracts, manuscripts, and presentations for external scientific meetings

- Act as the clinical science lead to CROs and external vendors, with appropriate oversight from senior leadership

- Contribute to a culture of innovation, collaboration, and continuous improvement

- Perform additional responsibilities as assigned by leadership

**Qualifications**

- Doctoral degree required (PhD, MD, PharmD, PsyD, MA, LCSW)

- Minimum of 3 years of clinical development experience

- Experience in CNS development (psychiatry or neurology) strongly preferred

- Strong understanding of late‑stage clinical development and regulatory processes

- Experience in data review, analysis, and regulatory writing (e.g., IND and CTD sections)

- Demonstrated ability to work collaboratively across functions

- Excellent written and verbal communication skills

**Other Skills & Requirements**

- Managerial experience a plus

- Proven ability to anticipate challenges and propose thoughtful, evidence‑based solutions

- Willingness to travel as required, including international travel (typically 10–20%, may reach higher during peak periods)

The starting base pay range for this position is $169,814.00 - $192,241.00. 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!

Associate Director, Clinical Development - MDD

Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.

Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.

The Commercial & Medical Counsel will act as a strategic partner to commercial and medical affairs teams, helping translate complex regulatory requirements into practical guidance that enables compliant commercialization. We are looking for a personable legal advisor with an understanding of the False Claims Act; Food, Drug & Cosmetic Act; Anti-Kickback Statute; and other healthcare laws and regulations. You will have high visibility throughout the organization, supporting core business activities and providing counsel to cross-functional teams. You will be empowered to develop strong and positive working relationships with colleagues at all levels. Experience in pharmaceutical / life sciences advising, ability to work in a fast-paced environment, and willingness to be a flexible, business-oriented team player are required. The role reports to the Associate General Counsel.

**Responsibilities**

- Provide day-to-day legal counsel to Sales, Marketing, Market Access, Medical Affairs, HEOR and Patient Advocacy teams, advising on a broad range of regulatory matters, including labeling discussions, advertising and promotion, drug safety, market research, scientific exchange, and interactions with healthcare professionals and patients

- Participate as a core member of promotional and medical MLR Review Committees, and advise on advertising, promotion, and scientific exchange

- Advise on interactions with healthcare professionals, payers, patients, and patient advocacy organizations, and help identify and mitigate compliance risks

- Review and/or draft contracts for compliance with relevant regulatory standards

- Ensure compliance with all relevant laws, regulations, policies, procedure and controls within relevant business areas supported

- Develop and deliver training for business partners on legal and compliance issues

- Communicate legal advice to business stakeholders in an authentic and understandable way

**Requirements:**

- Juris Doctorate and admission to practice law in at least one state

- Minimum 5 years legal experience, including experience advising pharmaceutical or other life sciences clients is required. In-house pharmaceutical industry experience is preferred

- Understanding of applicable laws and regulations, particularly FDA promotional guidance, the Anti-Kickback Statute and False Claims Act, the PhRMA Code, and relevant HHS-OIG guidance

- Strong interpersonal skills and ability to present complex information accurately and concisely to influence others at all levels of management

- Experience with state price reporting, transparency reporting or privacy matters preferred

- Ability to provide clear, actionable guidance in a fast-paced environment and handle multiple, conflicting priorities and time-sensitive situations

- High degree of professional ethics and integrity

The starting base pay range for this position is $217,877.00 - $260,733.00. 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!

Director, Commercial & Medical Legal Counsel

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