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Job Details

CRA - regional Travel - UK

Company: RBW Consulting
Location:
Reference: SI-CRA-31
Closing Date: 23 Dec 16
Type: Permanent
Salary (£): 30,000 - 40,000
Benefits:

Job Summary:

We have an exciting opportunity for developing your skills in Clinical Research as a CRA based in the UK, if you are interested in a new challenge then this role will be ideal for you! The successful candidate will have the opportunity to work across numerous complex trials within a broad spectrum of therapeutic indications, and will receive outstanding continued provision and training to aid you with the best progression within the organisation.

Requirements:

Type: Permanent

We have an exciting opportunity for developing your skills in Clinical Research as a CRA based in the UK, if you are interested in a new challenge then this role will be ideal for you!

The successful candidate will have the opportunity to work across numerous complex trials within a broad spectrum of therapeutic indications, and will receive outstanding continued provision and training to aid you with the best progression 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

Ideal Candidate Profile:

  • Active development in at least two therapeutic areas
  • Positive working both independently as well as in a team
  • Some skills within leadership actions
  • Ability to review protocols, CRFs and other Project- related data collection tools
  • Capability to develop and maintain BMS and other related tracking systems
  • Good communication skills to discuss, present results in meetings to senior members or trial statisticians

This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be. Please contact Sayful Islam on +44 (O)1293 584 300 or email a CV to sayful.islam@rbwconsulting .com.

Keywords: Clinical Research Associate Senior CRA project manager contract clinical trials CRA II clinical research clinical cra, scra, cpm, clinical, clinical research, clinical research associate, pharmaceuticals, biotech, cro, pharma, senior clinical research associate. UK, United Kingdom, England, Scotland, Wales, Northern Ireland

 

Apply for this job: CRA - regional Travel - UK

Contact Information:

Address:  Brighton
Southdown House, 130a Western Road, Brighton BN1 2LA
BN1 2LA
England
Tel:  01293 584 300

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