Clinical Research Associate

Job Type:
Clinical Research
Job Category:
Salary Description:
Competitive Salary Offered
Job Ref:

If you are looking for great career progressions and to develop your skills in Clinical Research then the role being offered by my client will be of interest to you! 

Due to a period of exciting growth within the USA, my client is seeking to appoint SCRAs and CRA IIs to work in various locations. The successful Clinical Research Associate will have the opportunity to work across several complex trials within numerous therapeutic indications, and will receive excellent continued support and training so as to best progress their career within the organisation.

Main responsibilities:

  • Monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards.
  • Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
  • Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
  • Assist with study protocol design, development and / or review if required
  • Complete and compile all necessary research, documentation and information to gain appropriate regulatory and ethical committee approval where required
  • Perform pre-study initiation, interim monitoring and close out visits as required
  • Carry out drug formulation administration procedures and documentation records
  • Ensure adequacy of drug shipment and drug accountability
  • Liaise with the Medical Monitor, Principal Investigator, clinical operations staff and sponsor representatives as required
  • Organise/attend investigator meetings as required
  • Provide support to the Project Manager / Country Manager with ad-hoc tasks as required

Skills/Experience: • Educated to degree level in Sciences/Life Sciences degree • Minimum of 2 years independent monitoring • CRO or Pharma experience • Excellent command of English language and local language, additional languages are highly desirable • Experience in regulatory submissions, contract negotiations, site management and feasibility assessment • Valid driving licence and ability to travel

This is a fantastic opportunity offering the successful candidate a permanent position within a reputable organisation.

As specialists in the placement of candidates within the Pharmaceutical Industry, our service is thorough, proficient and intelligent.  With over thirty years’ experience in the recruitment industry we, at Barrington James have an exceptional reputation that we intend to keep at the highest level by continuing our expert ways of working at a professional level.  As a company we pride ourselves in our expert, consultative, realistic approach

For further information about this role and to be considered as an applicant, please get in touch with or call on +1 646 415 8221

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Contact Details:
Tel: +1 646 415 8221
Contact: Taylor Ahearne

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