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Clin Res Assoc II

Employer
Labcorp
Location
Maidenhead, United Kingdom
Salary
Competitive
Start date
4 Oct 2019
Closing date
3 Nov 2019

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Job Details

This Position isPermanent and Home based anywhere in the UK.



Covanceis looking to recruit a UK based monitor (to work in multiple therapeutic areas)- at CRAIIlevel.



This would suit a home based CRA who already has independent monitoring experience within pharma or CRO - or perhaps in the NHS or academic setting and who would be looking to broaden their monitoring skills in the commercial environment.



This role offers excellent exposure to a range of disease areas and a real chance of career progression and promotion opportunities in time.



Positions within the UK Covance Clinical Operations department are able to provide a fantastic environment for development and growth.



Covance is committed to the well-being and development of its employees and one of the key selling points of the UK Clinops group is its strong Management Team and great supportive team spirit between all the colleagues.



Time and again staff comment on their amazing colleagues in Covance Clinops UK and the camaraderie of the department, with many people starting their careers or joining us, developing and remaining with us for many years.



The UK Management team constantly review study/site allocations and workload to actively balance with wellbeing of staff,and take actions to address where needed working closely with project teams, unlike a lot of other CROs.



Our people are our cornerstone and we believe strongly in looking after them and their ambitions and act to do so accordingly.



We offer Office (Edinburgh or Maidenhead or Leeds) and field-based positions.



Full time or part time



We benefit from working on multiple phases and therapeutic areas, also including more rare and unusual ones, allowing varied experience to be gained in the environment of the Clinops aspect of Covance
  • Phases I - IV
  • Working to changing/different Protocols and more diverse study types
  • Therapeutic Areas: CV, Oncology, Metabolic, Neuroscience, Rare Disease, Paediatric, Medical Devices, General Medicine, Infectious Diseases
  • Lots of opportunity to broaden one's Therapeutic Area CV, including now being integrated with legacy Chiltern Biopharma and Oncology groups with opportunities to work across both Agile Biotech and Large Pharma
  • Client facing tasks/opportunities are also available in the Clinops environment for those with an interest in this



Development:



Cross-development into other departments across the organisation, a key factor in our retention!



Global experience is gained for development towards CTL and PM positions



Working within Clinops can allow for a faster tracked pathway to the above roles - candidates can be put forward for the CTL Mentoring/Training scheme and Project Management Academy, both Covance initiatives committed to retaining and developing our talented Clinops staff



Within UK Clinops itself there is also the opportunity to mentor junior CRAs and help to develop our home grown talent - In-house CRAs (IHCRAs) who have aspirations to become CRAs - by becoming involved as a trainer in the well regarded Covance Monitoring Excellence Academy and performing onsite training visits.


  • Please send your CV and cover letter to marc.joseph@covance.com or call Marc on 01753 216664 for further information and discussion
Education/Qualifications:
Minimum Required:
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
  • Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
  • Thorough knowledge of monitoring procedures
  • Basic understanding of the clinical trial process
  • Valid Driver's License

Preferred:
  • Thorough knowledge of Company SOPs regarding site monitoring
Experience:
Minimum Required:
  • A minimum of 2 years of Clinical Monitoring experience is preferred, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job can be substituted.
  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, and local regulatory Guidelines
  • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Good planning, organization and problem-solving abilities
  • Ability to work with minimal supervision
  • Good communication and interpersonal skills
  • Good analytical and negotiation skills
  • Computer competency
  • Fluent in local office language and in English, both written and verbal
  • Works efficiently and effectively in a matrix environment

Preferred:
  • One (1) or more additional years of experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred, however an equivalent combination of education and experience to successfully perform the key responsibilities of the job.

Locations:
Maidenhead, United Kingdom

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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