Senior Clinical Program Director

Jobright.ai; Houston (TX); On-site; USD 100,000 - 120,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

An AI-powered career platform is seeking a Senior Clinical Program Director to join a pioneering medical device startup focused on mental health solutions. The role involves designing strategies for clinical evidence generation and overseeing clinical studies to ensure compliance with regulations. Candidates should have over 10 years of experience in the medical device industry, particularly with implantable devices, and possess a strong background in clinical research management.

Qualifications

• 10+ years of experience leading clinical research programs in medical devices.
• Proven success in designing and executing clinical trials for implantable devices.
• Experience managing CROs and developing KOL relationships.

Responsibilities

• Develop and maintain global clinical evidence plans.
• Create and manage multi-year evidence roadmaps.
• Lead execution of industry-sponsored clinical trials.

Skills

Leadership in clinical research

Regulatory knowledge

Collaboration with cross-functional teams

Management of medical professionals

Education

Bachelor's degree in engineering, science, health science, or nursing

Job description

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Jobright is an AI-powered career platform that helps job seekers discover the top opportunities in the US. We are NOT a staffing agency. Jobright does not hire directly for these positions. We connect you with verified openings from employers you can trust.

Job Summary:

Motif Neurotech is a medical device startup focused on developing innovative solutions for mental health conditions. They are seeking a Clinical Program Director to design and execute strategies for clinical evidence generation that supports regulatory approval and product validation, while collaborating with cross-functional teams and external partners.

Responsibilities:

• Develop and maintain global clinical evidence plans aligned with therapy objectives, product development milestones, and regulatory requirements.

• Create and manage multi-year evidence roadmaps addressing both pre-market and post-market study needs.

• Design clinical studies that support product claims, regulatory submissions, and long-term therapy adoption.

• Lead execution of industry-sponsored clinical trials in collaboration with CROs, specialized vendors, and consultants.

• Oversee study design, site strategy, patient recruitment, and data quality to meet regulatory and product performance goals.

• Manage timelines, budgets, and operational risks with proactive mitigation strategies.

• Ensure studies are delivered on time, within budget, and in compliance with GCP, ISO 14155, and applicable regulations.

• Work closely with Leadership, Market Access, Regulatory, R&D teams to ensure study design supports product development and approval strategies.

• Collaborate with clinical scientists and biostatisticians on endpoint selection, statistical analysis plans, and data interpretation.

• Identify, engage, and develop relationships with global and regional KOLs to guide clinical strategy and enhance program credibility.

• Partner with KOLs to refine study design, endpoints, and recruitment strategies.

• Foster long-term KOL relationships to support ongoing evidence generation, scientific exchange, and therapy adoption.

Qualifications:

Required:

• Bachelor's degree in engineering, science, health science, nursing, or related field.

• 10+ years of experience leading clinical research programs in the medical device industry, including study management.

• Proven success designing and executing industry-sponsored clinical trials in implantable medical devices or interventional psychiatry that achieved regulatory or launch milestones.

• Strong experience in identification, development, and management of medical professionals and KOLs.

• Experience managing CRO and multiple vendors.

• Familiarity with device regulations, GCP, and ISO 14155.

Company:

Motif Neurotech is a company that develops minimally invasive bioelectronic implants for monitoring and treating severe mental illnesses. Founded in 2022, the company is headquartered in Houston, Texas, USA, with a team of 11-50 employees. The company is currently Early Stage.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Product Management

• Industries

  Software Development

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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