Director, I&I Clinical Development (Non-MD)

Pfizer; Cambridge (MA); Híbrido; USD 177.000 - 294.000; Jornada completa

Descripción de la vacante

Pfizer in Cambridge, MA seeks an experienced clinical development leader to coordinate and drive multiple studies for novel therapies across development stages. You will guide protocol design, lead cross-functional study teams, and ensure enrollment, safety, and data quality in collaboration with Biostatistics, Regulatory, Clinical Operations, and other partners.

The role demands a PhD/PharmD or equivalent with extensive experience in clinical development, strong scientific writing and

Formación

• PhD/PharmD with 5+ years in clinical development or MS with 7+ years, with milestones.
• Strong scientific writing, presentation, and verbal communication skills.
• Experience coaching cross-functional teams and driving stakeholder alignment across all levels.

Responsabilidades

• Provide scientific leadership for the design, execution, and interpretation of clinical studies, delivering high-quality trial execution and meaningful outcomes.
• Lead development and execution of clinical development programs, operating independently within project teams.
• Lead preparation of clinical protocols, informed consent forms, investigator brochures, SAPs and regulatory documents.
• Lead clinical data review activities, including safety and efficacy data analyses for safety review meetings.
• Develop publications, abstracts, and scientific communications; support study teams with strategy and milestones.

Conocimientos

Scientific writing

Presentation skills

Verbal communication

Cross-functional collaboration

Leadership

Educación

PhD/PharmD

MS

BSc

Herramientas

CORD

JReview

Signal Management

GDMS

pTMF

Descripción del empleo

Pfizer in Cambridge, MA seeks an experienced clinical development leader to coordinate and drive multiple studies for novel therapies across development stages. You will guide protocol design, lead cross-functional study teams, and ensure enrollment, safety, and data quality in collaboration with Biostatistics, Regulatory, Clinical Operations, and other partners.

The role demands a PhD/PharmD or equivalent with extensive experience in clinical development, strong scientific writing and