| Job Field | Grade | Speciality | Region | Actions |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | Berkshire, Buckinghamshire,... | Details |
| In this role you will be responsible for the planning, implementation and conduct of large, complex clinical trials or multiple smaller studies across indications or for a single development compound. The Senior Clinical Project Manager is expected to provide leadership within the department and to make recommendations with regards to the strategic aspects of Clinical Operations... [Full Details] |
| Salary: Negotiable |
| IT & Data Management | Any Grade | Data Management | Hertfordshire (United Kingdom) | Details |
| My client is a research-focused global healthcare company that discovers, develops and provides innovative diagnostic and therapeutic products and services to deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnosis, treatment, and treatment monitoring.
We are currently looking for a Data Manager (DM) to be a part of... [Full Details] |
| Salary: 30000 - 35000 £ |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical... | Leicestershire (United Kingdom,... | Details |
| Field based Study Operations role with Blue Chip company now open
Do you want to gain exceptional experience working within a leading team? Do you want to work for an International pharma who have expertise in Cardiovascular, Oncology, Inflammation and Infectious Disease? If so then please read on for your opportunity to progress your career.
Our client, is looking to recruit a Senior... [Full Details] |
| Salary: Negotiable (200 - 270 £) |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | Leicestershire (United Kingdom,... | Details |
| Our client a major force in global drug development seeks a regional Senior CRA to work home based within the UK. The initial contract is for 6 months, and you will need to be set up to work from home and be willing to monitor hospital and GP centers across the UK. For regional roles you must already have a settled home location and Broadband ready to function.
Duties:
Conduct effective... [Full Details] |
| Salary: Negotiable (150 - 200 £) |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Bedfordshire (United Kingdom) | Details |
| An exciting 6-month Contract Role for a regulatory affairs consultant has come up in Bedfordshire.
You will be responsible for delivering and maintaining regulatory licences for UK/Ireland/Malta commercial brands and meet Regulatory Compliance Requirement for defined product and project responsibilities.
You will ensure timely submission of all licencing applications and compliance with... [Full Details] |
| Salary: 240 - 300 £ |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | Middlesex (United Kingdom) | Details |
| CSL have a new CONTRACT to fill. If you wish to be considered or know of someone who might we'd be delighted to hear from you today with any referral (form attached).
3 month assignment for a Project Manager who has Safety Process Experience. Located in West London, Immediate start call now if you qualify and wish to be considered.
Project Manager (International Safety Affiliate... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | Bedfordshire, Hertfordshire (United... | Details |
| Global Study Manager required for contract role with Global Pharma in Herts.
Overview:
Provides the operational expertise and leadership to one or more clinical operations teams to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases of Clinical Study Management (Plan, Initiate, Conduct, Close), in accordance with the appropriate... [Full Details] |
| Salary: Negotiable (370 - 400 £) |
| Clinical Research | Any Grade | Clinical Study Coordinator, Clinical... | Bedfordshire, Hertfordshire (United... | Details |
| A great opportunity for an experienced CTA who has worked on GLOBAL studies to join a leading pharma company in Herts on contract.
This role will form part of a close-nit global study management team and would be the ideal opportunity for someonewho is keen to get into project/study management. Bright graduates in this role have progressed into study and project managers without monitoring... [Full Details] |
| Salary: Negotiable (210 - 250 £) |
| Clinical Research | Any Grade | Clinical Study Coordinator, Clinical... | West Sussex (United Kingdom) | Details |
| Work in Clinical Pharmacology and Translational Medicine with a leading Pharmaceutical company located in South-East England.
You will be responsible for planning and implementation all operational aspects of the Translational Medicine (TM) studies. In this role you will lead medium to high complexity studies; first in man, patient studies, multi-center studies and possibly mechanistic... [Full Details] |
| Salary: 40000 - 50000 £ |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical... | Berkshire, Oxfordshire (United... | Details |
| Feeling your role is no longer a challenge or too pigeon holed to allow you any flair or global reach? Maybe you are itching to manage your own trials now from concept to reporting but constrained due to portfolio or competition? Don't despite a smaller company environment can offer breadth and risibility beyond the corporate matrix and this role located outside London is a superb chance to... [Full Details] |
| Salary: Negotiable (Up to 55000 £) |
| IT & Data Management | Any Grade | Data Management | Berkshire, Oxfordshire (United... | Details |
| PERT/Gantt your thing? Working in drug development at the interface between preclinical and FIH/PoC trials. Then this Project Manager, Project Management - Discovery to POC will be the role for you. Permanent Position with a growing biopharmaceutical company.
The Project Manager is responsible for compiling the activities, time lines and budget coordination associated with our Client's... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Surrey, Middlesex (United Kingdom) | Details |
| Job Summary
The role of the Regulatory Affairs Manager within Emerging Markets is to facilitate product global registration and life cycle management by executing regulatory strategies for initial product registration and throughout product lifecycle
Responsibilities:
Use expertise in IE markets to provide input into product strategy for the IE region
Preparation of International... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | Berkshire, Buckinghamshire,... | Details |
| Fantastic opportunity to engage in a 12 month contract with our client, a global pharma company in Bucks. You will be required to manage the UK portion of a Phase 3 dermatology study with the potential of setting up and running a Phase 1 study.
Duties:
You will already have study/project management experience from a Pharma or CRO and will be competent in the following:
Budget proposal for... [Full Details] |
| Salary: Negotiable (325 - 380 £) |
| IT & Data Management | Any Grade | Data Management, Programmer | Essex, Hertfordshire, Middlesex... | Details |
| Immediate start contract role located in Herts with one pharmaceutical client. This contract is PAYE direct hire on a salaried basis for 12 months initially. You must be working in the UK in a similar role already in industry to apply and be available to start work within 1- 4 weeks.
Serve to give programming support for pharmacokinetic and modelling & simulation projects.
Tasks:
-... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, CRM, Clinical... | Any Location (Germany) | Details |
| An exciting opportunity for a Clinical Trial Management System Coordinator (CTMS) to work on contract with a major pharmaceutical firm.
This role is an office based role in Germany and is for a 6 month duration.
You will be responsible for contributing to the update, maintain and support the CTMS/IMPACT system and support the system end users. This includes providing training, assistance,... [Full Details] |
| Salary: 3000 - 35000 £ |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, QA | Hampshire, Wiltshire (United Kingdom) | Details |
| Our client's business model relies on their excellent relationships with their vendors. Outsourced manufacturing is a critical part of their success an hence they need excellent in-house staff to support this model. The QA team are specialised across functions, and a new role has opened in GMP QA.
The Senior QA Associate will be responsible for working with vendors (CMO's), supporting... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | Derbyshire, London, Wiltshire (United... | Details |
| Excellent field-based CRA role with major pharma. Experience in Diabetes or Oncology would be a real advantage in this position.
Our client is one of the few companies with their own CRA team in the UK and this role is rare. The planned start date is Sep 2010, as the client is planning ahead to make sure that they get the best individuals on their team.
To be considered you must... [Full Details] |
| Salary: Negotiable (200 - 250 £) |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | West Midlands, Wiltshire (United... | Details |
| Our global pharma client is recruiting competent CRAs for one of their new CNS studies to start Sept/Oct. This is an initial contract position with a strong possibility of extension.
This will be a great opportunity for a CRA who is currently working full time, home based, or looking to move into a home based position. Site locations will be in Swindon, Southampton, Oxford, Cardiff, Preston,... [Full Details] |
| Salary: Negotiable (200 - 250 £) |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | London, West Midlands (United Kingdom) | Details |
| Excellent field-based CRA role with major pharma to monitor sites in Midlands. Experience in rheumatoid arthritis or oncology would be a real advantage in this position. The current workload is 11 sites, locations are:
Derby, Middlesborough, Stoke, Manchester, Bromwich, Cannock, Cardiff, Harrogate, London.
Our client is one of the few companies with their own CRA team in the UK and this... [Full Details] |
| Salary: Negotiable (200 - 250 £) |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | Berkshire, Surrey, Warwickshire... | Details |
| Our Global Pharma client is seeking a competent, field based CRA covering the South of England (The ideal candidate will be based no further North than Birmingham and close to good transport links). This is an immediate full-time position on an initial 12 month contract. Ideal candidates must have previous experience as a CRA working within a Pharmaceutical company or a CRO. All therapeutic... [Full Details] |
| Salary: Negotiable (250 - 280 £) |
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