- PW 6335 Global Submission Specialist / Regulatory Submissions Project Manager
Opportunity for a Submissions Manager to join this Top 20 Pharma on a fixed term contract as our Client’s Global Regulatory Submissions Specialist. The role is office based in the South East, focuses on compliant submissions, Ectd standardisation and sits within a cross functional global team. Contract length is 6 months and strong likelihood to extend further.
- PW 6360 Interim Regulatory Manager, Neuroscience
Our global pharmaceutical client is looking for an interim Regulatory Manager to support a major, key neuroscience project in their global regulatory affairs group. This has numerous maintenance activities with major milestones in 2015 which require a regulatory professional experienced in life cycle management, including Type 1A/B variations, Type II variation (CMC), PSUR submission, Management of Linguistic review & PIP annual reports
- PW 6274 Senior CPM / Senior Clinical Project Manager / Oncology Trials
Opportunity to join this energetic, ambitious and growing Global CRO at Senior CPM level. Remit is to manage international Oncology trials, at Phase II and III. Office based from the Global HQ, this role will involve mostly EU travel and is offered on a permanent and full-time basis. Fantastic development opportunities once on-board.
- Regulatory Affairs Specialist/ Project Manager
An IVD company based in Cardiff are looking for an interim RA Specialist on a 6 - 12 month contract with the potential to extend further.
- Project Manager (Commercial Portfolio Development)
Permanent position for a Project Manager (commercial) with global pharma company to start asap. Competitive salary offered!
- PW 6315 Senior Clinical Project Manager
Opportunity to join an entrepreneurial global pharmaceutical company as Senior Clinical Project Manager. You’ll operationally lead project activity, supervise trial personnel and deliver on set objectives. Exceptional collaborative and interpersonal skills are required for this pivotal cross functional role. The role is office based to the West of London.
- Medical Information Scientist & Medical Education Manager
Exciting permanent opportunity for an experienced medical affairs professional as a Medical Information & Medical Education Manager - competitive salary available!!!
- PW 6346 European Study Manager – Oncology
An excellent opportunity for an experienced Clinical Research professional to join one of our leading Oncology focused clients. As Study Manger, you will be responsible for the management and co-ordination of EU trials with full oversight of required vendors. This is a pivotal role within a small and specialised Biotech who have received global recognition for their diverse portfolio.
- Medical Liaison Manager Respiratory (Global)
Medical Liaison Manager Respiratory (Global) Munich (Full relocation and accommodation available)
- PW 6326 Compliance Manager (10 months FTC)
This is an excellent opportunity for an experienced compliance professional to join this global pharmaceutical company’s newly established, growing compliance group. You will play a pivotal role in ensuring the compliant and efficient operations in the UK with respect to ABPI Code Compliance, and other laws and regulations including GxP.