Director of Global Regulatory Pre‑Award Strategy

Worldwide Clinical Trials; England; Sur place; GBP 80 000 - 120 000; Plein temps

Résumé du poste

Worldwide Clinical Trials is seeking a Director, Regulatory Pre-Award Strategy. In this leadership position, you will oversee regulatory affairs activities and ensure compliance across projects. You will provide expert advice to both internal and external stakeholders and lead a team in the preparation of regulatory documents.

The ideal candidate has a strong background in clinical research and demonstrated leadership within the pharmaceutical industry. This is an opportunity to join a pioneering CRO dedicated to improving lives.

Qualifications

• Minimum four-year degree in relevant science.
• Eight years in clinical research with regulatory experience.
• Ten years in pharmaceutical/CRO industry is required.

Responsabilités

• Oversees regulatory affairs activities and staff.
• Provides expert regulatory advice for projects.
• Responsible for regulatory compliance and documentation.

Connaissances

Strong oral and written communication skills

Leadership and organizational management

Proficiency in MS-Office applications

Understanding of clinical research principles

Interpersonal skills in fast-paced environments

Formation

Four-year college curriculum in medical/sciences

Nursing degree or equivalent life science degree

Outils

MS-Office applications

Description du poste

Worldwide Clinical Trials is seeking a Director, Regulatory Pre-Award Strategy. In this leadership position, you will oversee regulatory affairs activities and ensure compliance across projects. You will provide expert advice to both internal and external stakeholders and lead a team in the preparation of regulatory documents.

The ideal candidate has a strong background in clinical research and demonstrated leadership within the pharmaceutical industry. This is an opportunity to join a pioneering CRO dedicated to improving lives.