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Job Details
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Senior Manager Clinical QA - New Jersey - Pharma

Business Type: Pharmaceutical Company
Job Type: Quality Assurance - Control
Job Level: Management
Position: Full Time
Location: USA - New York
Reference: DAFE#14804
Closing Date: 22/05/19
Job Details:

Senior Manager Clinical QA - New Jersey - Pharma

Senior Manager, Clinical QA required to work for a busy and exciting medium to large sized Pharmaceuticals organization. They are a fully integrated Pharma (end-to-end) company and have made a highly reputable name for themselves in the oncology and neurology space.

This position will be based on their New Jersey site located in Woodcliff Lake.


Senior Manager Clinical QA / Snr Manager CQA


USA / New Jersey / Woodcliff Lake


Highly competitive salary (DOE)


  • You will be the "go to" person for assuring a high level of quality on projects, as defined in Federal Regulations, local regulations, GCP, company policies and applicable industry standards
  • In a nutshell - you will conduct global clinical site and GCP document audits and author audit reports
  • As the Senior Manager Clinical QA you will assist with regulatory inspections, GCP projects and provide GCP training, manage contract GCP auditors, Author and independently manage Audit Programs
  • Importantly, you will ensure quality improvement through the communication of audit results and compliance guidance


  • A proven track record and 7 years (minimum) GCP Quality experience
  • Bachelor''s degree in a science discipline
  • In depth Knowledge of GCP requirements, regulations and Quality
  • Be open to travel 25% of the time
  • Recent experience including clinical site/CRO, clinical/regulatory and/or document auditing
  • Meticulous with written skills and experience of prioritising / planning
  • Unparalleled communication skills and the ability to influence others
  • Be real life "self-starter"


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the USA, Europe and Asia Pac. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.


If you would like to discuss this vacancy further, please call Senior Recruitment Consultant David Fearnley on +1 (718) 514-9604, or email If this role is not suitable, David is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Senior Manager Clinical QA / Snr Manager CQA / Vendor Quality Oversight / USA / New Jersey / Infectious / Mahwah / NJ / GXP / Regulatory / Validation / Qualification / SOP / Quality / QA / GCP / Vendor / CRO / Florham / Clinical / CRA / Monitoring / QA / Risk / Report / Training / Oversight / Sponsor / Site / Travel / Goods Clinical Practice / Woodcliff Lakes / Audit / TMF

i-Pharm Consulting Posted by:: i-Pharm Consulting (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 15/05/2019 | NPJ Ref: 235724
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