We are currently recruiting for a Senior GCP Auditor to join our top 10 global CRO. You will be responsible for the full life cycle of audits from planning audits through to hosting them. This role will require carrying out vendor/system/facility/investigative audits across many therapeutic areas. This role also involves much travelling across Europe.
My client is a top US biopharma with an exceptional pipeline of drug candidates which are at crucial stages in clinical trials. They are seeking a GCP QA senior specialist to perform GCP audits and maintain GCP quality systems in house. Reporting to a Senior Manager you will get to work in an environment with exceptional training, development and on truly ground breaking drugs which will improve patient lives for generations to come. ...
An expanding and developing global pharmaceutical company is actively seeking a Senior Quality Assurance professional with GCP/PV and/or CSV experience for a brilliant new opportunity based in the South East of the UK. Ideally, the professional within this role will be experienced within CSV and will provide CQM input and guidance for the CSV activities and provide approvals as applicable.
I am currently working with one of the most exciting and progressing Biopharmaceutical companies globally to recruit a Senior Manager for their Quality Assurance Team. This professional will have oversight of the GCP and PV QA operations and will provide expert analysis on where the teams can move forwards. The ideal candidate will be an experienced GCP/PV professional, ideally with auditing experience in both areas. Management experience is also advantageous.
A Leading Global Pharmaceutical Company, are presently looking to bring in a Regulatory Affairs Clinical Specialist to be based in the West London Office.
Coordination of routine submissions to ensure timely delivery and ensuring the content is appropriate to each individual regulatory agency while maintaining compliance with Company policy and procedures as they apply to the role. ...
Clinical Research Associate II - Italy
The client, a global Clinical Research Organization our offering an exciting new opportunity as a Clinical Research Associate (CRA). You will be responsible for monitoring all types of clinical trials ensuring adherence to Good Clinical Practices (GCP), investigator integrity and compliance with all study procedures.
The Clinical Research Associate I (CRA I) is accountable and responsible for all aspects of site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites within the approved Clinical Development Plan (CDP).
The Clinical Research Associate I (CRA I) is accountable and responsible for all aspects of site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites within the approved Clinical Development Plan (CDP)
PPD is currently seeking a Manager of Internal Audits, to join our Global Quality & Compliance department.
This position sits with the Internal Audit team, and will have oversight of this function and a team of Auditors, in the EMEA region.
Pharm-Olam International are actively looking for a Senior Clinical Research Associate (SCRA) to join our team in Switzerland on a full time, permanent basis. Ideal candidates will have at least 3 years clinical monitoring experience from a CRO background.
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