- Project Manager – International Medical Affairs
Our client International Medical Affairs Department is devoted to optimizing patient benefit by generating and communicating compelling scientific evidence that demonstrate the value of their medicines. It channels the research and development of their products into real life clinical practice, and is partner of choice for healthcare professionals. It protects patients’ safety and welfare, applying the highest standards of ethics compliance and integrity.
- Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Regulatory Affairs Manager \ Regulatory Affairs Project Manager \ Regulatory Submissions
Our client is a leading global contract research organisation providing drug discovery, development and lifecycle management services. Their clients and partners include pharmaceutical, biotechnology, medical device, academic and government organisations.
- 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.
- Clinical Project Manager – Early Phase R&D, Oncology
JOB TITLEClinical Project Manager – Early Phase R&D, OncologyROLE DESCRIPTIONThis is a rare opportunity for a Clinical Project Manager. Someone who is innovative by nature and who wants to be a part of an exciting arm of one of the world’s leading Pharmaceutical companies.As Clinical Project Manager – Early Phase, you will be driving the development of ground-breaking products through Phase I & II studies or programs of oncology studies. ...
- Early Phase Development – Project Manager, NBEs - Hertfordshire
My client is an international pharmaceutical company with an acclaimed product portfolio and a stable development pipeline. With a novel R&D wing located in Hertfordshire, the company is in search of an experienced early phase development project manager to oversee the companies' oncology study program.
- Pharmacovigilance Project Manager – Slough/Thames Valley/Berks
Pharmacovigilance Project Manager - Slough/Thames Valley/Berkshire/BuckinghamshireA Pharmacovigilance Project Manager is required to join a global leading organisation and be part of a dynamic fast paced team, leading the way within drug safety. This position will allow you to use your previous experience within pharmacovigilance and progress your career to the next stage.
- Drug Safety Project Manager – Buckinghamshire/Berkshire
JOB TITLE - Drug Safety Project Manager - Buckinghamshire/BerkshireA drug Safety Project Manager Position has become available within a Global CRO. This exciting Drug Safety Project Manager position will be the perfect fit for the following candidate who is looking to take the next step within their career or for someone that already has Drug Safety Project Management experience and looking for a fresh challenge within a dynamic organisation
- Drug Safety Project Manager – Buckinhamshire/Berkshire
Drug Safety Project Manager - Berkshire/BuckinghamshireDrug Safety Project Manager required to join a global world leading company. A solid understanding of drug safety is required for the candidate to be successful within this Drug Safety Project Manager role.
- Drug Safety Project Manager – Berkshire/Buckinghamshire
Drug Safety Project Manager - Berkshire/BuckinghamshireAn exciting opportunity has arisen to join a global CRO as Drug Safety Project Manager. This position will allow you to use your previous experience within drug safety and progress your career to the next stage within a fantastic organisation that is rapidly expanding.
- Project Manager - Biometrics
ROLE DESCRIPTION:As Project Manager you will bring experience managing in a matrix organisational structure and contribute to new systems, processes and SOPs for this European Biometrics CRO. You will have knowledge and experience across phases I-IV of clinical development and provide cross functional leadership in relation to clinical trial requirements. ...