Hybrid Clinical Development Director

Pfizer Inc; Collegeville (PA); Ibrido; USD 240.000 - 400.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid work

Medical benefits

Retirement plan

Descrizione del lavoro

Pfizer Inc. is seeking an experienced physician to provide medical monitoring for one or more clinical trials, guiding investigators and ensuring data integrity.

You will lead protocol development, safety assessments, and regulatory submissions while collaborating with cross-functional teams across the development lifecycle. The role requires a medical degree, several years in clinical research, and the ability to communicate complex medical concepts to stakeholders, investigators, and

Competenze

• MD or equivalent medical degree from an accredited school.
• 4+ years in biopharma clinical research
• Strong knowledge of ICH-GCP and regulatory expectations
• Excellent communication with investigators and stakeholders

Mansioni

• Provide medical monitoring on one or more clinical trials and supply study-related medical guidance.
• Lead clinical execution and contribute to protocol design and amendments as needed.
• Review safety data, SAP, and data trends; support audits and inspections.
• Coordinate with cross-functional teams to ensure TMF and regulatory readiness.
• Interact with Health Authorities and Ethics Committees as required.

Conoscenze

Clinical trial oversight

Medical data review

Healthcare communication

Regulatory knowledge

Formazione

MD/DO/MBBS/MBChB

Descrizione del lavoro

Pfizer Inc. is seeking an experienced physician to provide medical monitoring for one or more clinical trials, guiding investigators and ensuring data integrity.

You will lead protocol development, safety assessments, and regulatory submissions while collaborating with cross-functional teams across the development lifecycle. The role requires a medical degree, several years in clinical research, and the ability to communicate complex medical concepts to stakeholders, investigators, and