Director, Legal

Mineralys Therapeutics
United States
Remote

Who this role is best for

Best suited to experienced legal professionals with a background in pharmaceutical or biotechnology industries working in a remote, fast-paced environment.

Best fit for

  • Legal professionals with 6+ years in pharma or biotech and a focus on commercial and medical compliance
    — “6+ years of legal experience within the pharmaceutical, biotechnology, or life sciences industry”
  • Candidates who have supported product launches, especially in pre-commercial or newly commercial biotech companies
    — “Experience supporting a product launch, ideally with a pre-commercial or newly commercial biotechnology company”
  • Individuals comfortable with autonomy and cross-functional collaboration in a remote setting
    — “This is a hands-on role for an attorney who is comfortable giving clear, practical advice in a fast-moving, remote environment and appreciates autonomy”

Things to consider

  • Up to 10% travel is required, which may be outside the local area and involve overnight stays
    — “This position requires up to 10% travel. Frequently travel is outside the local area and overnight.”

How to stand out

  • Highlight experience in reviewing HCP and patient-facing materials for regulatory compliance
    — “Experience reviewing HCP and patient materials, and advising on patient support programs”
  • Emphasize your ability to balance legal risk with business objectives in your resume and interviews
    — “Provide advice across pre-launch and launch activities, balancing legal risk with business objectives”
  • Demonstrate your understanding of FDA and FTC regulations in promotional and medical materials
    — “Serve as the Legal representative on the PRC and MRC, reviewing HCP-facing, patient-facing, medical, and corporate materials for compliance with the Federal Food, Drug, and Cosmetic Act, FDA advertising and promotion regulations, FTC requirements, and other relevant and applicable industry codes”
Pace · Fast PacedCollaboration · HighAutonomy · HighDecision Impact · Company

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • successful legal review of promotional and medical materials
  • advice across pre-launch and launch activities
Typical background
6+ years of legal experience within the pharmaceutical, biotechnology, or life sciences industry

Skills & requirements

Required

Legal ReviewFDA Advertising And Promotion RegulationsCommercial Legal RequirementsCross-functional Interaction

Preferred

Patient Support Programs

Stack & domain

Legal ReviewPromotional And Medical Materials ReviewAdvertising And PromotionMedical Affairs ActivitiesCommercial OperationsMarket Access InitiativesProduct Launch PlanningFDA Advertising And Promotion RegulationsCommercial Legal RequirementsPatient Support ProgramsInterpersonal SkillsCross-functional InteractionClear, Practical AdviceAutonomyCommunicationLeadershipPharmaceuticalBiotechnologyLife SciencesHealthcare

About the role

Original posting from Mineralys Therapeutics via Greenhouse

“Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone.  Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor.  Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky”

Mineralys is a fully remote company.

Director, Legal

The Director, Legal (Commercial and Medical Review) will serve as the lead legal reviewer for promotional and medical materials. This individual will represent Legal in the Medical, Legal, and Regulatory (MLR) review process, will sit on the Promotional Review Committee (PRC) and Medical Review Committee (MRC), and will help design the standards and procedures that allow the company to review materials quickly, through planned launch and into commercialization. This is a hands-on role for an attorney who is comfortable giving clear, practical advice in a fast-moving, remote environment and appreciates autonomy.

Reporting to the VP, Commercial Legal, this role is accountable for providing practical legal guidance across advertising and promotion, medical affairs activities, commercial operations, market access initiatives, and product launch planning.

This role requires strong interpersonal skills and significant cross-functional interaction across Commercial, Medical Affairs, Regulatory, Legal and Compliance. Experience with patient support programs and related materials would be an asset to the role.

Key Responsibilities

Serve as the Legal representative on the PRC and MRC, reviewing HCP-facing, patient-facing, medical, and corporate materials for compliance with the Federal Food, Drug, and Cosmetic Act, FDA advertising and promotion regulations, FTC requirements, and other relevant and applicable industry codes

Provide advice across pre-launch and launch activities, balancing legal risk with business objectives

Review patient materials, including patient education, disease awareness, website and digital content, and patient support program communications, to ensure compliance with relevant regulations

Evaluate claims for substantiation, fair balance, and net impression, including comparative, subgroup, and pharmacokinetic claims, and provide clear direction to reviewers and authors

Advise on pre-approval communications, including scientific exchange, disease awareness, medical education, congress activity, and the boundaries between investor and corporate messaging and promotion of an investigational product

Review non-promotional and medical affairs materials, including responses to unsolicited requests, payor and formulary communications, and digital and social media content

Provide guidance on compliantly navigating the regulatory landscape in business activities such as disease education, HCP engagement, and patient-facing materials

Support corporate legal matters and business development initiatives as needed

Qualifications

JD from an accredited law school and active membership in at least one U.S. state bar

6+ years of legal experience within the pharmaceutical, biotechnology, or life sciences industry

Strong knowledge of FDA advertising, promotion regulations, and commercial legal requirements

Knowledge of product launch planning and commercialization activities

Experience reviewing HCP and patient materials, and advising on patient support programs, including hub services, co-pay assistance, and nurse or educator programs

Experience supporting a product launch, ideally with a pre-commercial or newly commercial biotechnology company

Core Competencies

Strong business judgment with a practical, solutions-oriented approach to risk management

Ability to balance legal risk and apply appropriate mitigation strategies

Ability to influence and advise in a matrixed environment

Excellent communication skills with the ability to translate complex legal and regulatory concepts into actionable business guidance

Strong cross-functional collaboration and relationship-building skills

Demonstrated ability to operate effectively in a fast-paced, resource-constrained environment

High degree of autonomy, accountability, and execution focus

Travel

This position requires up to 10% travel. Frequently travel is outside the local area and overnight.

This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level.

US Salary Range:  $200,000 - $232,000

#LI-Remote

Source: Mineralys Therapeutics careers (Greenhouse)

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