Medical Director, Clinical Science

Summary

Join N-Power Medicine as a Medical Director, Clinical Science and contribute to the design and development of clinical and translational research programs. Collaborate with pharmaceutical and biotechnology sponsors and internal teams to evaluate project feasibility, review patients, and ensure the success of ongoing projects. Provide medical support, including internal education and input on AI projects. This remote position within the US requires strong collaboration skills and experience in pharmaceutical sciences and clinical drug development. You will work with key opinion leaders, develop protocols, and serve as a medical monitor for clinical studies. The role also involves ensuring compliance with GCP, IRB guidelines, and FDA regulations.

Requirements

• 5+ years of experience in pharmaceutical sciences, clinical drug development, real world data generation, and/or clinical trial design and execution
• MD or MD/PhD with subspecialty training in oncology
• Proven ability to navigate highly matrixed environments, managing multiple stakeholders and priorities
• Strong track record of successfully executing projects under tight timelines
• Exceptional interpersonal skills, with the ability to engage and influence senior stakeholders, clinical teams, and technical experts
• Strong writing and oral communication skills
• Generous, Curious and Humble
• Ability to travel, up to 15%, may be required

Responsibilities

• Work to build key relationships with Key Opinion Leaders in academia and in the community setting
• Work with our pharma unit, data analytics, and clinical operations on feasibility assessments for new projects
• Work with pharma partners on the development of new projects when N-Power input is required
• Provide medical input for new projects including resource assessments, data generation requirements, protocol development, and implementation strategies
• Help with setting up new pre-screening automation tools and help with manual review of patients identified in pre-screening efforts
• Help drafting, reviewing, and overseeing the process of finalizing presentations, posters and key manuscripts for work arising from N-Power’s efforts
• Develop protocols and serve as medical monitor for clinical studies in the N-Power network
• Work collaboratively with Legal, Compliance, and Clinical Operations teams to ensure well-documented policy and procedures that comply with Good Clinical Practice (GCP), Institutional Review Board (IRB) guidelines, and FDA regulations
• Work closely with other N-Power teams to support submissions, audits, and inspections when appropriate
• Other duties as assigned

Benefits

• The expected salary range for this position is $230,000 and $260,000
• Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law
• N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance
• This position is eligible for company benefits
• 401K plan