- Clinical Compliance Project Manager
Are you looking to work in one of the most exciting areas of medical science? Are you keen to ensure that you are working for a company that are a leader in their field? Is working with unique technologies something that drives you? If so, then continue reading to find out just how suitable this opportunity may be for you.
- International GCP/Clinical QA Auditor – Leading Global CRO – Home-based
A leading global full-service CRO operating in UK, Europe and the US, they are a leader within their field. Offering Phase I-IV clinical research services using leading technologies to provide a bespoke service to match the needs of their clients.
- PW 6235 Clinical QA Officer / GCP Quality Assurance Officer
Opportunity to join a growing Pharma organisation as Clinical QA Officer. You’ll need a background in Clinical monitoring, clinical auditing or compliance and the role comes with excellent developmental opportunity.
Office based to the West of London, offered on a permanent basis.
- International GCP Auditor/QA Auditor – Global CRO – Warsaw, Poland
GCP Quality Assurance Auditor - This is a great opportunity for an experienced GCP Quality Assurance Auditor to join a leading global Mid-size CRO. This full service, global CRO are offering this great opportunity to progress and further your international QA auditing experience.
- Regulatory Compliance PV Manager
An exciting opportunity has arisen for a Regulatory Compliance PV Manager to join a global biopharmaceutical company based in Cambridge. A very patient focused company, who scientific research has resulted in 15 marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. ...
- Regulatory Compliance PV
A senior person within Regulatory Compliance PV is wanted to join my client, a leading global biopharmaceutical company. You will be joining their International Compliance team.
- **ASSOCIATE DIRECTOR GCP QUALITY ASSURANCE - GERMANY**
One of my best clients is currently recruiting for an Associate Director of GCP, Quality Assurance and R+D. This role will see the right individual directly manage R&D GCP QA staff based in Europe and works with other global team members to ensure the upkeep of all Quality Assurance areas within the company. With a wide range of activities and responsibilities, this role is perfect for an individual who is organized, hardworking and passionate about Quality Assurance.
- **Clinical Quality Assurance Officer**
A top Pharmaceutical client of mine is actively seeking an experienced Clinical Quality Professional to join their team based in Berkshire, in the UK. The role is a Clinical Quality Assurance Office and you will be reporting into the Director of Quality. Ideally, you will have audit experience, systems experience and also have supported inspections. This role can offer a fantastic platform for development within Quality Assurance, and the company can provide a brilliant structure for this.
- Director GCP Compliance – Massachusetts, US
Exciting new position with a dynamic Biotech business based in Industry hub - Massachusetts, US.
- Clinical Research Assistant II Job
Manage Investigative Site activities to ensure that subject safety is protected and that timely high quality data are collected in compliance with regulationsResponsibilities include, but are not limited to:1. ...