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Job Title: Project Manager - (EDC) Clinical Trials
Salary: £40,000 - £55,000 + excellent benefits
Territory: South West London Base
Experience in CRO or Pharma Project Management (qualified) will be considered
Our client is a pioneering developer of specialist technology solutions for the pharmaceutical industry. They work globally with some of the largest pharmaceutical companies and contract research organisations in the world, providing the software which drives essential…
Clinical Research Nurse -Newly Graduated Nurses - Midlands
Clinical Research Nurse required by Clinical Research Organisation based in the Midlands. Are you a recent graduate?? This is an excellent opportunity for a Registered Nurse (RGN) to develop a career in the exciting Clinical Research/Pharmaceutical sector. A generous salary is on offer for the successful candidate. No industry experience necessary.
Clinical Research Nurse / Clinical Trial Nurse / Research Nurse
You will participate in the planning, preparation and conduct of clinical trials carried out according to ICH-GCP guidelines…
Clinical Research Associate
Our Client is a Clinical Research Organisation (CRO) specialising in medical device clinical research.
They have helped in the successful completion of over 400 clinical trials involving medical device products. In addition, their medical writers have helped to prepare many scientific papers for publication in international journals.
With a well established network of investigators in Europe and North America, co-ordination of multi-national studies is one of their strengths. As a company that undertakes in-house clinical research as well as multi-site clinical trials, they have a thorough understanding…
Our client is a highly respected research led Pharmaceutical company who are seeking a Senior CTA for their central London offices.
The primary purpose of the CTA is to administer, maintain and co-ordinate the logistical and administrative aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). They also act as a pivotal point of contact & support for the clinical trial team.
Main duties / responsibilities (in order of priority)
1. Preparing essential clinical trial documentation, distributing, tracking and filing of documents on return.
2. Arranging & participating…
Mcginley Scientific have an exciting opportunity for an experienced Clinical Research Associate (CRA) ,to work under limited supervision, monitors and oversee clinical practices for one or more multi-site international clinical trials, ensuring compliance with all regulatory agency requirements, ICH-GCP and SOPs.
The successful CRA requires the conviction to use their own initiative, coupled with a challenge.
Minimum requirements for the CRA include:
Sound knowledge of methodology, procedures and principles of clinical trials and European regulations and guidelines pertaining to their conduct.
Science degree or a nursing qualification…
Clinical Trials Assistant-Pharmaceutical-Permanent-Oxford-£25-30k
We require an experienced Clinical Trials Assistant (CTA) to join a pharmaceutical company in Oxford on a permanent basis, responsible for providing administrative assistance to the Clinical Department by supporting the Clinical Programme Manager and Clinical Operations team on all clinical studies. You will have previous experience working within Clinical Research and will preferably be educated to degree level.
*Set up and maintenance of Study Shadow File
*Develop and maintain tracking tools to assist with "oversight" of study (e.g. contact lists…
Clinical Research Associate (CRA) / CRA II - UK Home or Office based - Permanent - Excellent salary + car allowance / company car + benefits package
Clinical Research Associate (CRA) / CRA II opportunity to join a market leading Global CRO in the UK on a permanent basis. This can be home or office based throughout England and offers an excellent salary plus benefits package including company car or car allowance.
The Clinical Research Associate (CRA) / CRA II / Senior CRA will have a varied role working on global clinical studies in a range of therapeutic indications including Oncology, HIV etc and phase trials. Main responsibilities…
Job Title: Project Manager - eClinical Trials
Salary: up to £55,000
Territory: London Base
Clinical Research Project Management Experience Required
Our client is a successful market leading organisation providing solutions for more efficient paper free clinical trials. Their products improve patient engagement through the development and deployment of intuitive and patient-focused eCOA technology.
We have an urgent need to hire an organized, team oriented, excellent time manager…
Clinical Research Associate (Dutch or German speaking)
An exciting opportunity has arisen to join a successful CRO as a Clinical Research Associate, working in oncology research. The successful candidate will be responsible for monitoring and reporting on the progress of phase I – III clinical trials that will be happening across Europe. It will be necessary for the candidate to liaise with clients in either Dutch or German.
Our client is a leading CRO which assists in all aspects of clinical research, and offers their specialist services globally.
• Working experience as a Clinical Research Associate
Clinical Research Associate (CRA) / Senior CRA
This exciting new opportunity presents an opportunity for a Swedish/Danish speaking CRA to work from the UK monitoring trails in both the UK and Scandinavia. The position will be responsible for a broad range of CRA duties as well as helping with certain aspects of business development to increase the company’s share of the market in Northern Europe.
Our client is a leading CRO with an international focus in providing professional services in pharmaceuticals, medical devices and diagnostic tests.
- Practical CRA experience
- Speaking Swedish…
Senior Clinical Data Manager
An exciting opportunity has arisen to join a leading CRO as a Senior Clinical Data Manager, working in the field of oncology. The successful candidate will be responsible for independently leading clinical data management activities across a range of assigned projects with minimal supervision.
Our client is a leading CRO which assists in all aspects of clinical research, and offers their specialist services globally.
• Extensive working experience in a clinical data management role
• Excellent working knowledge of GCP standards
• Experience of managing the data management plan
Position: CTS Programme Manager
Salary: £35,000 to £45,000
As the CTS Programme Manager you'll be the department point of contact and provide operational and strategic support for clinical trial programmes. You'll cover a large scope from the planning stages, through the operational activities and drug supply management during the lifecycle of the trial.
*Establish an excellent working relationship within the clinical team in order to full understand the needs for the trial.
*Help guide the team in the design of the packaging and labelling ensuring cost effective options.
An excellent opportunity has arisen to join a world leading global organisation, our client Unilever are currently looking for a Female Clinical Trials Technician based at Unilever's manufacturing site in Seacroft, Leeds. This is a full time temporary role for a period of 12 months initially, working a 37.5 hour week. This role is paying up to £19,026 pro rata, depending on experience. Due to the sensitive nature of the role and close contact with other women, we will be recruiting female, non-smokers only!
The Clinical Trials Technician role is an excellent opportunity for a science graduate with exceptional people skills to join Unilever…
Clinical Programme Manager-ICH-GCP-CRO-Permanent-Oxford-up to £70k + excellent benefits
A fantastic opportunity has arisen for a talented Clinical Programme Manager to join a pharmaceutical company in Oxford taking project management responsibility of all clinical aspects of outsources clinical studies to ensure successful completion of studies on time and within budget. You will have previous experience in clinical project management of international clinical trials and will hold a degree in life sciences.
Key responsibilities include:
*Project Management of all clinical aspects of company's outsourced clinical studies
QA GCP Manager
This is an exciting and challenging position for a QA GCP Manager who will be responsible for managing quality systems and ensuring quality standards are met across a range of clinical studies. The successful candidate will line manage a QA team and will be responsible for managing internal and external audits.
Our client provides a niche consultative service to the clinical market, by recommending or implementing structure around their clients’ clinical documentation. Based in Buckinghamshire, our client offers an empowering working environment with the chance to make a real difference, internally…
Respiratory Nurse Advisor
Salary up to circa £33,000 depending on experience
Plus 1k annual bonus and 10% of annual salary bonus. Car or Car allowance
We have vacancies in the following territories:
We are looking for Nurses to work within the fields of Asthma and COPD. You will be working for a company committed to improving patient outcomes by providing highly qualified disease management experts. Their Specialist Nurse Advisors have a passion for the disease area and an in-depth understanding of national treatment guidelines. They help healthcare professionals deliver the most…
Nurse Advisor; Respiratory (COPD & Asthma)
Salary up to c £34,000 and up to 10% of salary bonus,
Company car or car allowance and generous benefits package.
Are you a Registered Nurse looking for a new career?
We are looking for a Registered/Staff Nurse to specialise in Asthma and COPD. You will be working for a company committed to improving patient outcomes by providing highly qualified disease management experts. Their Specialist Nurse Advisors are passionate about respiratory care and help healthcare professionals deliver the most up to date care for patients. They have designed…
Oxford, Oxfordshire UK
£competitive + Benefits
Adaptimmune is a global, clinical-stage biopharmaceutical company with a research base in the heart of Abingdon. Due to rapid growth plans and new developments we are seeking a Director of Facilities and Building Projects to oversee the Facilities strategy, and management for all of our UK and US Facilities.
Adaptimmune are a forward thinking world leader in the development of T-cell based therapies for the treatment of cancer and their lead product is in early stage clinical trials against multiple tumour types. Operating in Oxford (UK) and Philadelphia (USA), the company…
Our client based in Staffordshire are pleased to offer the role of Head of Product Development based at their local site.
The role is working full time and will offer a salary of £60,000+ DOE.
The ideal candidate will have the below skill set:
Degree in food sciences
Experience working with a major food manufacturer
Experience with Sports, Clinical and Dairy Nutrition
Team Management Skills
Be Innovative and motivated
Responsibilities of the job will also include:
planning, organising and overseeing process or production trials
making improvements or modifications to current processes
formulating new production processes or stages…
Position: ADME Project Manager
Salary: £40,000 - £45,000
An excellent opportunity has arisen for an experienced ADME Project Manager to work within an innovative research-based pharmaceutical company specialising in unique medicine. You'll join the preclinical team and be part of a growing company which have big plans for the future.
As the ADME Project Manager you'll have overall management of the ADME and Pharmacology programmes from design, management and reporting of ADME and Pharmacology studies to GLP regulations and companies SOPs. You'll contribute across a verity of technical areas from IND…
As the Director of Quality
You will be responsible for:
The compliance of the Pharmaceutical Quality System to current EU requirements& awareness of future changes
The Quality Strategy aligned with client needs
Ensuring the release of batches of IMP products to clients/clinic within the requirements of 2001/83/EC as amended
To provide Quality Direction & Leadership
Quality System Compliance
Continuous Improvement of the Pharmaceutical Quality System
Client Audits and Regulatory Inspections
General Management of the Quality team
Qualifications, Skills and Experience
We are looking for the Director of Quality to be an…
Our client, a globally recognised Pharmaceutical company, has an opportunity for a Regulatory Affairs Clinical Trial Submission professional to join their European Regulatory Affairs department.
This position is responsible for managing Regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning five therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology and Infectious Disease).
The team is responsible for the Regulatory Affairs work in geographical Europe, Turkey, Israel, South Africa, New Zealand and Australia. The work has several aspects…
Clinical Research Physician Manchester.
Zest Scientific recruitment is continuing to expand a leading clinical research organisation in Manchester by recruiting a Clinical Research Physician. If you are looking to develop your career in the clinical research sector, working for a leading multinational organisation renowned throughout the industry for its meteoric rise to success and dependability to deliver on global contracts across multiple therapeutic areas and phases, then this role would be of interest. If you are already a clinical research physician and are looking to play an integral role in the future of medicine across the globe…
Based in Horsham, West Sussex this is an rare opportunity for a Clinical Trials Pharmacist or Clinical Trials Pharmacy Technician to utilise their skills and cross train into a broader Clinical Supply Chain Manager in a commercial environment. The Supply Chain Management team develop and deliver complex clinical supply chain strategies encompassing processes, procedures and standards that are utilised at multiple project, programme level. This role involves working with key strategic clients ensuring that all aspects of robust supply chain solutions integrate with the client`s processes and procedures. Full training…
Clinical Research Physician - mobile role.
Zest Scientific recruitment is continuing to expand a leading clinical research organisation in the UK by recruiting a Clinical Research Physician on a 12month contract. If you are looking to develop your career in the clinical research sector, working for a leading multinational organisation renowned throughout the industry for its meteoric rise to success and dependability to deliver on global contracts across multiple therapeutic areas and phases, then this role would be of interest. If you are doctor from the NHS or Private and are looking to play an integral role in the future of medicine…