[Hiring] Executive Medical Director, Clinical Development @IMVT Corporation

Role Description

The Clinical Development Leader – Neurology is a key role within Immunovant’s Neurology portfolio. This Clinical Development Leader will lead clinical trials for one or more of Immunovant’s development programs in neurology, specifically responsible for Immunovant’s ongoing major study for IMVT-1402 in CIDP.

For this critical position, the Clinical Development Leader will be the primary point person for medical oversight of clinical studies with responsibilities to include:

• Clinical trial design
• Site feasibility assessment
• Protocol development
• Clinical trial enrollment
• Sponsor medical monitoring
• Review and interpretation of clinical trial data
• Drafting key clinical documents such as protocol, CSR, briefing package, IND, NDA, BLA, etc.

This role will be responsible for timely execution of deliverables in close collaboration with relevant internal and external partners.

The successful candidate is driven, curious, patient-focused, collaborative, with a bold ambition to contribute to Immunovant’s mission to enable normal lives for people living with autoimmune diseases.

Qualifications

• A minimum of 8 years’ experience in early to late-stage development in an industry (CRO and/or Pharma) setting.
• Proven ability to plan and conduct clinical trials.
• Demonstrated track record in working effectively in cross-functional teams and work streams (pharmacovigilance, biostatistics, clinical operations, and regulatory affairs).
• Prior late phase clinical trial experience in neurology is highly desirable.
• Ability to thrive in a fast-paced environment.
• Proven ability to successfully manage multiple tasks and prioritize accordingly.
• Attention to detail, internal drive to generate high-quality work, and sense of passion and urgency to achieve team and program goals.
• Excellent analytical, problem-solving, and strategic planning skills.
• Strong interpersonal skills commensurate with the need to work closely with CROs, investigators, consultants, and team members across functions.
• Exceptional written and oral communication skills to meet the needs of varied audiences.
• Integrated understanding of FDA, EMA, ICH, and GCP guidelines. Prior interactions with FDA and EMA regulatory agencies would be desirable.

Requirements

• MD, DO, or non-US equivalent of MD degree.
• Board certification in Neurology is strongly preferred.

Benefits

• Salary range: $380,000 — $415,000 USD
• Compensation based on market location and job-related knowledge, skills, and experience.
• Equity and other forms of compensation may be provided as part of a total compensation package.
• Full range of medical, dental, vision, 401k, and other benefits.
• Unlimited paid time off and parental leave.

Work Environment

• Remote-based
• Dynamic, interactive, fast-paced, and entrepreneurial environment
• Domestic or international travel required (20%)