Associate Director, Clinical Quality & Compliance

BioSpace; Boston (MA); Hybrid; USD 153.600 - 241.340; Vollzeit

Benefits dieser Stelle

Health insurance

401(k) match

Paid vacation

Tuition reimbursement

Zusammenfassung

A leading global pharmaceutical company is seeking an Associate Director for Clinical & Quality Process Compliance. This role involves ensuring high-quality standards across processes and compliance with regulatory requirements. The ideal candidate will have significant experience in the pharmaceutical industry, particularly in Clinical Operations and GCP Quality. Responsibilities include managing regulatory procedures and leading compliance initiatives. Competitive salary and robust benefits package offered.

Qualifikationen

• Minimum of 7 years of responsibility in the global pharmaceutical industry.
• At least 3 years of experience in GCP Quality/Compliance.
• Advanced knowledge of FDA, EU, and GCP regulations.

Aufgaben

• Ensure compliance with Regulatory Intelligence Procedures.
• Maintain a robust communication plan regarding regulations.
• Provide data insights to regulatory compliance metrics.

Kenntnisse

Excellent communication skills

Critical thinking

Project management

Fluency in English

Ausbildung

BSc in a scientific, allied health, or medical field

Jobbeschreibung

A leading global pharmaceutical company is seeking an Associate Director for Clinical & Quality Process Compliance. This role involves ensuring high-quality standards across processes and compliance with regulatory requirements. The ideal candidate will have significant experience in the pharmaceutical industry, particularly in Clinical Operations and GCP Quality. Responsibilities include managing regulatory procedures and leading compliance initiatives. Competitive salary and robust benefits package offered.