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A global pharma company is looking for a Clinical Trial Manager (CTM) to join there team ASAP for a 6 month contract.
The role is office based in Berkshire, however they will have flexibility with some home working.
Background experience required:
* Knowledge of UK research environment
* 3 years experience within clinical research, preferably in a similar environment
* Scientific degree/ background
The roles will be right for either:
* A CRA looking for a more senior role or progression towards project management.
* Clinical Trial Manager -CRO or NHS trial manager looking to transition to Pharma
* Site start up manager
* A Senior…
Title: Clinical Research Associate - Senior Clinical Research Associate
Salary: 28,000 - 42,000 (experience dependent)
One of the top five Contract Research Organisation is looking for brightest talent to join their company. They have opportunities throughout the organisation, from being trained in house, to being contracted out working for a leading pharmaceutical company.
What is required?
Investigator identification and selection
Co-ordination of ethics committee and regulatory authority applications and approvals
Pre-trial procedures including collation of necessary documentation.
Organisation, attendance and/or presentations at…
Position: Clinical Research Associate
Location: Home Based - Northern England/Scotland
An exciting new opportunity has arisen for a Clinical Research Associate to join a growing Pharmaceutical company where you'll be responsible for the day to day activities including set up, monitoring and completion of clinical trials in accordance with SOPs and regulatory guidelines.
*Ensure the integrity of clinical data and adherence to applicable regulatory protocol and company guidelines.
*Ensure the rights, safety and wellbeing of clinical trial subjects is maintained.
*Perform site management…
Clinical Research Associate ( CRA- Surrey)
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…
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
Home based CRA
Zest Scientific are recruiting a CRA for a leading clinical research organisation in the UK. The Clinical Research Associate will be responsible for monitoring clinical trial sites to ensure compliance with the protocol, with GCP and with other appropriate regulations and guidelines, and will be the primary contact-point for Investigational Site staff. This CRA role can be home based with a couple of visits to the office per month
The responsibilities of the CRA will include:
monitoring of clinical study sites as appropriate, including pre-study, initiation, monitoring and close-down meetings with clinical study…
Research Nurse Manager
Full-time, 1 year Fixed Term Contract
Up to £46,000 per annum
Pulse has an exciting opportunity to offer an experienced Research Nurse the role as Research Nurse Manager within a well renowned Clinical Trials Unit in Central London. This will be a 1 year fixed term contract.
This impressive unit covers various specialities including:
• General Medicine
Within the unit, facilities are available for Phase I, II and III clinical testing of new drugs and novel techniques in these areas. The unit has consolidated its expertise and experience and has a proven track record…
An excellent opportunity has arisen to join a growing company as a Junior Project Manager. This role will involve the operational site management of clinical trials, as well as carrying out on-site monitoring activities. The successful candidate will also be responsible for ethical and regulatory submissions and preparing monthly study progress reports, as well as taking on a number of clinical project management responsibilities. This role can be on a permanent or contract basis, depending on the view of the candidate.
Our client is at the forefront of their industry and offers an excellent environment…
We are currently looking to recruit a Clinic Administrator for our Manchester site.
The Clinic Administrator provides essential administrative support to the Clinic Administration Manager, Clinical Trials Manager, (Senior) Research Nurses and (Senior) Study Physicians, and to the volunteers for hVIVO studies. This includes the management of the reception area within the clinical trial centre.
The ideal candidate will have solid experience of a similar type role within a clinical environment, Grade C or above in GCSE’s or equivalent, especially English, Science and Mathematics. Be a highly competent user in audio typing…
£34,000 - £38,000pa
Harley Street District
Purosearch are working in conjunction with a modern and state of the art private clinic in the infamous Harley Street district. The clinic boasts high tech and contemporary facilities in their research and trials within a variety of disciplines including asthma, allergies, COPD, urology and general medicine.
As a research nurse, the post holder will have previous research experience, show a clear passion for clinical trials and medical research.
The Research Nurse requires:
• RGN (current pin)
• 2 years+ post registration experience
• Demonstrative understanding of clinical…
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…
Clinical Programme Manager
We are currently recruiting a Clinical Programme Manager for one of our Medical Devices clients in the South East of England. This is a key role within the business which involves all aspects of the clinical research programme from concept feasibility through to product approval as well as medical communications. This is an area critical to the company's vision.
The role will involve significant internal and external communication, interacting with all departments in addition to healthcare professionals and academics on a global basis. A thorough understanding of clinical research along with an understanding of…
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
Designs or manages the implementation of the Physicians strategy within Clinical Development both regionally and globally
Uses expertise and knowledge of global issues to develop strategic Physicians objectives for inclusion into the company's annual business objective
Contributes to or manages the development of the senior management team in area of expertise
Provides expert advice in the area of specialism, influencing the development of statistics to the global business and Global Clinical Development
Closely follows medical developments within assigned areas and disseminates new information within Clinical Development…
Position - Clinical Study Manager
Location - Warwickshire
Salary - Unable to disclose on advert but highly competitive
This privately owned company, which was spun out from a FTSE100 engineering company, is looking for a Clinical Study Manager to join their growing team. The company has developed advanced haemodialysis systems for use both at home and in clinic and their product is seen as a "game changer" so this is an exciting opportunity for you to really make a difference to people's lives.
As a Clinical Study Manager you'll be involved with all aspects of clinical research and medical communications…
• Our client is a multinational class 3 medical device business, supplying a wide range of healthcare products into global markets.
• Business growth combined with the organisations commitment to further reinforce its market leading status, has created an opportunity for an experienced European Clinical Programs Manager
The European Clinical Programs Manager – role:
• To manage the clinical evaluation for new products and claim extension of existing products
• To manage the clinical trials or case study in supporting marketing activities
• To manage the Post Market Clinical Follow-up (PMCF) and Post Market Surveillance (PMS…
Nicholas Howard Limited are delighted to be recruiting for a new and exciting role as a Clinical and Post Marketing Safety Leader.
Based in Basingstoke, the successful candidate will be responsible for the oversight and conduct of audits in support of the pharmacovigilance system audit plan.
Responsibilities will include managing and conducting audit activities associated with pharmacovigilance and clinical trial safety, ensuring the appropriate corrective and preventative actions are completed in a timely manner and identifying any potential systematic gaps and assisting with the implementation of remediation. You will work with other R&D…
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…
Clinical Trial Supply Coordinator
Our client is a well established and expanding pharmaceutical service company that specialises in providing medicines to patients and their physicians. Due to ongoing success they are seeking to recruit a Clinical Trial Supply Coordinator.
The successful applicant will ensure the timely provision of Clinical Trial supplies through an audited and efficient supply chain under the direction of the line manager. You will ensure the best client service is offered and solutions from enquiry to delivery are provided to clients through the collaboration with the CTS sales team.
Supply Manager – Clinical Trials
Job ref: 18905
Our client is a well established and expanding pharmaceutical service company that specialises in providing medicines to patients and their physicians. Due to ongoing success they are seeking to recruit a Clinical Trial Supply Manager.
The successful candidate will be delivering the clinical trial project management support necessary to achieve the Clinical Trial Supply Group sales target, reporting to the Senior Clinical Trial Supply Manager.
Key Responsibilities will include:
Key Account Management, such as:
• Working closely with the BD team to identify, understand and manage Key…
Our client, a prestigious national private healthcare group, urgently requires a full time experienced Senior Registered Nurse to join their Oncology Department at a private hospital based in Surrey.
The Hospital comprises of 76 beds, 3 operating theatres, an ambulatory care unit which includes 2 Endoscopy/Minor Operation rooms, 6 bay recovery area and a Gynaecology/Urology minor procedures room.
Role Purpose & Core Responsibilities:
• The post holder will be responsible for ensuring that patients and visitors receive a level of service that conforms to BMI Healthcare vision, aspiration and values. He or she is responsible in ensuring…
Nurse Advisors; 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?
Territory; Essex/North London
Monday - Friday
These roles would suit a Practice Nurse with a strong respiratory background or Nurses who have worked in acute respiratory wards managing patients with severe asthma
We have 2 vacancies for Registered/Staff Nurses 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…
Position: ADME Project Manager
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…
Join Unilever as a Consumer Testing Technician at their site in Leeds (Seacroft LS14) and you'll be responsible for the running of the Hot Room, monitoring the panellists during tests to ensure their safety and wellbeing.
As a Consumer Testing Technician, you'll be responsible for dealing with all panellists in a professional, courteous manner. You'll set up the testing including: preparation of test products and set up the data capture system. You'll handle the application of deodorant products to panellist's underarm, accurately recording test results and provide analysis of the data.
Ideally, you'll have previous experience of research…
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…