CRA II - Single Sponsor

Location
Homeworking
Salary
Competitive + car allowance and benefits
Posted
10 Sep 2019
Closes
10 Oct 2019
Ref
GRT-SCRAII-SS199
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

I am currently working on several Single Sponsor home-based CRA II positions . In this role you will be working for a global leading CRO at Pharmaceutical companies working on innovative studies on a range of therapeutic areas and phases. If you are an experienced Clinical Research Associate looking for your next exciting opportunity please get in touch to discuss

Depending on your level of experience, typical duties and responsibilities will include:

  • 9 site visits a month - site management visits, including site· evaluation, initiation, routine monitoring and close-out visits
  • Ensuring the integrity of clinical data through maintenance of site tracking record
  • Building relationships with investigator site staff to ensure that key clinical metrics are met
  • Taking part in the development of assigned protocols and Case Report Forms
  • Assisting in on site co-monitoring visits with more junior members of staff, as required

In order to be considered for CRA positions, you will have:
 

  • Significant independent UK monitoring experience in a pharmaceutical company or CRO environment. Minimum 18 months
  • A life science degree or equivalent
  • Good knowledge of ICH-GCP guidelines and local and international regulatory requirements
  • Strong verbal and written communication skills
  • The ability to work independently and in a team

This is one of several positions in the field of Clinical Research that 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 Grace Ticehurst on 01293 584 300 or click Apply Now to submit your CV.

Keywords:

Clinical research associate | CRA | senior CRA | CRA II | clinical research | clinical monitor | pharma | biotech | study monitoring | clinical studies | clinical trials | regional monitoring | UK | United Kingdom | pharmaceutical 

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