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GCP Auditor Job

Eingestellt von Yoh

Gesuchte Skills: Natural, Client

Projektbeschreibung

A GCP AUDITOR is needed for a CONTRACT opportunity with Yoh's client located in Bridgewater, NJ.

TOP SKILLS YOU SHOULD POSSESS:

- Clinical Quality Assurance
- CRO Audits
- CQA SOP's

WHAT YOU'LL BE DOING:

- The GCP Auditor Principal Specialist is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Principal Specialist's mission and responsibilities, the audits and activities require proven ability to independently interact with all internal and external (eg Vendors/CRO) operational staff (eg Project Teams, Clinical Operations, Pharmacovigilance, etc.) involved in the audited Clinical Research activities
- The GCP Auditor Principal Specialist's responsibilities also include the mission of GCP Project Representative for the projects assigned by CQA Management.
- The position reports to the Team Manager of CQA. The GCP Auditor Principal Specialist may be assigned as temporary backup for the CQA Team Manager.
- Independently prepare, conduct, report, and follow-up on audits according to the departmental SOPs, the agreed audit strategy, audit program, and objectives. Audits include project/study related audits, audits of processes/systems associated with clinical research and audits of CROs
- Lead routine and directed audits
- Act as a GCP Project Representative (GCP PR) for assigned clinical projects

WHAT YOU NEED TO BRING TO THE TABLE:

- Bachelor degree preferably in a life/medical/natural sciences or scientific discipline
- 10 to 14 years of pharmaceutical (or related) experience with BA or 8 to 12 years with advanced degree, eg MBA, MS, PharmD, PhD. This includes a minimum of 6 years of Clinical Quality Assurance related experience and/or experience in Clinical Trials such as Monitoring or Clinical Trial Management with good performance
- Extensive working knowledge of international regulations/Guidelines/Good Practices pertaining to the clinical domain (Clinical Development, Pharmacovigilance and Regulatory Affairs)
- Good working knowledge of standard computer office software such as Word, Email system (Outlook, Lotus, etc.), PowerPoint and Excel

GET HIRED, APPLY NOW!

RECRUITER: Tonya Allen

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.

J2W: CLINICAL

MONJOBJ2WNECLIN

Ref:

SFSF: LS

Projektdetails

  • Einsatzort:

    Bridgewater, Vereinigte Staaten

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Yoh