VP, Medical Strategy & Clinical Development

Larimar Therapeutics, Inc.; Philadelphia (Philadelphia County); Presencial; USD 250.000 - 450.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Stock options

401K

Flexible PTO

Descripción de la vacante

Larimar Therapeutics, Inc. in Philadelphia seeks a Vice President of Medical to shape and execute clinical development, ensuring patient safety and data integrity.

You will lead cross-functional teams, review study data with regulators, and provide strategic medical direction across programs, with international travel as needed. The role requires an MD/DO, 10+ years in pharma with management experience, and strong leadership, writing, and regulatory knowledge.

Formación

• MD/DO medical degree required; neurology or cardiology background preferred.
• 10+ years in pharma with progressive management responsibilities.
• Experience in neurology and/or rare diseases preferred.
• Strong medical writing, presentation, and leadership skills.
• Good clinical practices (GCP) knowledge and regulatory familiarity.

Responsabilidades

• Lead medical guidance across clinical development programs with cross-functional teams.
• Review data with Statistics and provide interpretation for studies.
• Collaborate with Safety and Pharmacovigilance for medical input and safety.
• Support Medical Affairs activities and review program documents.
• Represent Medical in internal/external meetings and supervise staff.
• Ensure regulatory compliance and high data integrity across studies.
• Present medical information at site visits and congresses.
• Engage with external partners and regulatory bodies; travel as needed.

Conocimientos

Executive leadership experience

Medical writing

Strategic clinical development

Cross-functional collaboration

Regulatory understanding

10+ years pharma experience

Travel readiness

Educación

MD/DO medical degree

Descripción del empleo

Larimar Therapeutics, Inc. in Philadelphia seeks a Vice President of Medical to shape and execute clinical development, ensuring patient safety and data integrity.

You will lead cross-functional teams, review study data with regulators, and provide strategic medical direction across programs, with international travel as needed. The role requires an MD/DO, 10+ years in pharma with management experience, and strong leadership, writing, and regulatory knowledge.