Sr. Manager/AD, Clinical QA

COMPANY:

Biopharmaceutical company focused on the discovery, development and commercialization of novel medicines to meet needs in oncology and inflammation and autoimmunity.

LOCATION:

Wilmington, DE

RELOCATION ASSISTANCE:

Yes

TITLE:

Sr. Manager/Associate Director, Clinical QA (title will be dependent on experience)

TYPE:

Full-time, permanent

ROLE RESPONSIBILITIES:

The Manager/Senior Manager, Clinical QA provides global audit support and GCP oversight of Clinical Operations teams to the Head of Global Clinical QA. The Manager/Senior Manager executes and manages Clinical QA-GCP audits and GCP guidance and advice across assigned departments across the company's Clinical groups.

CANDIDATE REQUIREMENTS:

• Bachelor's degree
• 5 - 10 years' experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role with a minimum of 3 years' experience performing GCP audits of CROs and investigator sites.
• Strong written and oral communication skills.
• Prior Regulatory inspection experience desired.
• Ability to travel up to 30%.

If you meet the requirements above and would like to be considered for this position, apply on-line now to be contacted with further details.