Strategic Clinical Development Director, Autoimmune CAR-T

Crispr Therapeutics Inc in; Boston (MA); Presencial; USD 290.000 - 315.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

On-site work three days a week

Descripción de la vacante

CRISPR Therapeutics, Inc. in Boston, MA is seeking an Executive Director, Clinical Development (Project Management) to lead clinical strategy, mentor leads, and drive multiple studies in auto-immune programs. You will design trials, review data, and present to leadership and safety oversight committees.

The role requires an MD with advanced rheumatology training and 15+ years of related experience, plus strong communication and collaboration across functions.

Formación

• MD with advanced rheumatology training and licensure.
• 15+ years in clinical or related research.
• Proven mentoring and leadership in a matrix environment.
• Excellent oral and written communication and analytical skills.

Responsabilidades

• Develop the clinical development strategy for autoimmune programs and study designs.
• Mentor clinical development leads and author/review key study documents.
• Review safety and efficacy data and provide assessments and recommendations.
• Build relationships with thought leaders, investigators, and partners.
• Serve as clinical development lead for one or more studies and communicate results.
• Collaborate with operations, statistics, safety, and regulatory teams to translate protocols.
• Review literature and competitive intelligence to shape strategy.
• Develop training materials and prepare scientific presentations.
• Lead drafting/regulatory submissions and generate data-driven slide decks.

Conocimientos

Leadership

Communication

Analytical thinking

Mentoring

Educación

Medical Doctorate (MD)

Advanced rheumatology training

Descripción del empleo

CRISPR Therapeutics, Inc. in Boston, MA is seeking an Executive Director, Clinical Development (Project Management) to lead clinical strategy, mentor leads, and drive multiple studies in auto-immune programs. You will design trials, review data, and present to leadership and safety oversight committees.

The role requires an MD with advanced rheumatology training and 15+ years of related experience, plus strong communication and collaboration across functions.