About Medivant Healthcare
Medivant Healthcare is an FDA-registered 503B pharmaceutical manufacturer with over $40 million invested in CGMP-compliant facilities to produce pharma-grade compounded medications.
We are launching the first prefilled syringe (PFS) testosterone product line designed for both men and women, including the first-ever microdose injectable testosterone specifically formulated for female patients.
With no FDA-approved testosterone product currently available for women in the United States, Medivant is positioned to responsibly establish a new therapeutic category serving over 55 million peri- and post-menopausal women nationwide.
Position Summary
We are seeking a clinically experienced Nurse Practitioner (NP), Physician Assistant (PA), or Physician (MD/DO) with experience in women’s health and hormone therapy to support our growing testosterone portfolio.
The ideal candidate is a clinician who has sat across from peri-menopausal women, witnessed their struggles with fatigue, low libido, and cognitive fog, and felt the frustration of limited evidence-based treatment options. You understand the clinical importance of testosterone in women’s health and are motivated to help build the responsible infrastructure needed to expand access safely and compliantly.
This role will serve as a clinical resource to providers, support medical education initiatives, and assist in developing practical prescribing guidelines and patient monitoring protocols. The position will work closely with leadership, marketing, and compliance teams to ensure accurate, evidence-based, and 503B-compliant medical communication.
This is a unique opportunity to play a foundational role in launching and shaping a new therapeutic category in women’s health.
Key Responsibilities
- Serve as a clinical liaison to healthcare providers prescribing testosterone therapy
- Support development of evidence-based dosing and patient monitoring protocols
- Assist with educational materials and training for providers
- Participate in advisory discussions with select physician partners
- Support CME content development in collaboration with accredited providers
- Attend key conferences (NAMS, ACOG, ISSWSH, regional OBGYN meetings) as company medical representative
- Review medical and training materials for clinical accuracy and 503B compliance
- Provide guidance to nurse educators and clinical outreach teams
- Support development of clinical data collection initiatives (e.g., chart reviews, outcomes tracking)
Qualifications
Required:
- NP, PA, MD, or DO with active U.S. license in good standing
- 2+ years of clinical experience in women’s health, OBGYN, endocrinology, menopause care, or hormone therapy
- Experience prescribing or managing hormone therapy (including testosterone preferred)
- Strong understanding of patient counseling and monitoring protocols
- Comfortable educating other healthcare providers
- Basic understanding of regulatory and compliance boundaries in medical communication
Preferred:
- Experience in menopause or sexual health medicine
- Experience working with compounded medications or 503B pharmacies
- Participation in professional organizations (NAMS, ISSWSH, ACOG, etc.)
- Experience speaking at local or regional clinical events
- Familiarity with testosterone therapy for women
Role Highlights
- Be part of launching a new women’s health therapeutic category
- Work with an FDA-registered 503B manufacturer
- Collaborate directly with executive leadership
- Opportunity for growth as the medical function expands
- Potential performance-based incentives
