- Medical Writing & Publication Manager - 3 days/week - Monday to Wednesday - 12 month Fixed Term Contract
Who we are
We’re innovation, curiosity and diversity – multiplied by 92,500 professionals in 150 countries. As a global leader in research-focused healthcare, we’re constantly learning and growing – and seeking people who share these goals. ...
- Associate Clinical Trial / Study Manager – 12 Month Contract – South East England – £320 per day
We are recruiting for an Associate Clinical Trial/Study Manager for a 12 month contract, office based in South East England. The role will be a supporting position for the Study Manager, managing vendors and dealing with budgets and timelines. The contract has a very strong likelihood of extensions and would be a great step up for a Lead CRA or Associate Study Manager, at an industry-leading company.
- Clinical Trial Manager – 12 Month Contract - £400+ per day
We are looking for an experienced individual to work as a Clinical Trial Manager for a global pharma working on Phase III trials. CRO management will be a large part of the role so experience in this is key. This role is office based in the South East and is an initial 12 month contract. This is a great chance to join an exciting team with a growing pipeline and with a high chance for contract extension and professional development within a contract.
- Clinical Project Manager - Dutch/Belgian Border
Clinical Project managerLocation: Dutch/Belgian borderType: contract/freelance Duration: 12 monthsStart date: ASAPHours per week: 40A global health care company based near the Dutch/Belgian border is looking for a Clinical Project Manager with experience in the Pharmaceutical, Biotech, Health care or Medical device industry. Ideally you have experience in all phases of the study life cycleThe Project Manager will work in a team of 10-20 people and you will manage the CRA’s. ...
- Associate Group Leader/Lab Supervisor, Small Molecule-124832
Supervisor (Associate Group Leader), Small Molecule
PPD is a leading contract research organisation that works with numerous pharmaceutical companies across the world. PPD has worked with 47 the top 50 pharmaceutical companies and over 750 biotechnology companies. The PPD facility in Athlone was set up in 2009, this purpose built GMP lab facility features a wide variety of GMP testing capabilities and specialised platforms. ...
- Operational Change Manager / ERP Change Manager
Operational Change Manager / ERP Change Manager - Earn up to £366 per day plus benefits (PAYE) or £474 per day (LTD)Our Global Pharmaceutical client is looking for an Operational Change Manager / ERP Change Manager to join their team in Middlesex for 6 months, to ensure that ERP template changes are effectively managed from a business perspective and are delivered effectively and in a timely manner
- Medicine and Process Delivery Project Manager / Project Manager
Medicine and Process Delivery Project Manager / Project Manager - Earn up to £318 per day plus benefits (PAYE) or £412 per day (LTD)Our Global Pharmaceutical Client is looking for a Medicine and Process Delivery Project Manager/Project Manager to join their team in Hertfordshire for 12 months, ensuring project plans are designed and delivered to time, cost and quality, giving guidance to teams, from initiation to close out phases.
- Associate Group Leader/Supervisor, BioPharm-133318
Due to the expansion in 2016 of our Ireland labs following continued success and growth, PPD is currently looking to recruit an Associate Group Leader to be based in our Biopharm department of our GMP Lab in Athlone, Ireland. Key responsibilities:
Management of a team of analysts
Allocation, scheduling and managing laboratory resources for group's project activities and updates LIMS for project status. Reviews timesheet reports for billing accuracy. ...
- Clinical Trial Submissions Manager - Belgium - Growing Brand
Clinical trial submissions manager - Trial, Study, Research CRA, Clinical trials, Submissions, Monitoring, Study, Research, Clinical Project manager, RA, Regulatory affairs, RegulationsMy growing biotech client is in urgent need of a mid to Senior level Clinical Submissions manager, someone proactive, confident, articulate and able to work with CRAs and clients in the field alike. Strong Regulations and stakeholder management exposure. ...
- Key Account Manager - Reduced Time - Ophthalmology - S Central
Our client is an international Healthcare Company that consistently tops employee satisfaction surveys and are hailed as pioneers in the development and treatment of many far reaching conditions including diabetes, Haematology, Neurology, Oncology, Ophthalmology and span into Animal Health and Radiology. They have a Key Account Manager opportunity to work with their Ophthalmology products preferably 3 days per week (Wed - Frid).