Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds RSS Feed PharmiWeb Candidate Blog RSS Feed PharmiWeb Client Blog

Job Details

CRA for mid size CRO

Company: Barrington James Clinical
Location: home/office based
Reference: FD45456S
Closing Date: 11 Dec 16
Type: Permanent
Salary (£): Competitive

Job Summary:

The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. You will be responsible for ensuring the overall integrity of assigned studies through the use of independent judgement and expertise.




The offer:

  • Professionalism, integrity and responsibility
  • Become member of a dynamic and growth-oriented organization
  • Conduct high quality trials
  • Benefit from good long-term scope for progression
  • Competitive remuneration package
  • Enjoy all benefits for permanent employment



  • Good interpersonal skills
  • Good monitoring skills to independently conduct all types of site monitoring visits
  • Proficient  computer skills, including Microsoft Office
  • Comprehensive knowledge of GCP/ICH guidelines
  • Able to exercise judgment within defined procedures and practices and to determine appropriate action independently.
  • Problem-solving skills
  • Ability to work in a matrix environment
  • Good time management and organizational skills

Your experience:

The ideal candidate is someone who

  • Has least 3 years experience.
  • Proves his skills in mentoring and training of other CRAs in a positive and effective manner.
  • Provides support to Project Team and Clinical Operations Team.
  • Is experienced in clinical research monitoring (including pre-study, initiation, routine monitoring and closeout visits) in international trials.
  • Verifies that the investigator, staff, and site facilities remain adequate throughout the trial period.
  • Serves as primary contact for assigned research sites.
  • May conduct site and study feasibility assessments.
  • Has good planning, organization and problem solving abilities
  • Manages and motivates sites to meet study goals.
  • Attends and participates in team teleconferences and training.
  • Makes recommendations for improvement in processes.
  • Is fluent in German and English.

If this sounds good to you then send your CV to, detailing your qualifications and previous experience. You can also call our office in Frankfurt am Main under +49 274 015 840 and ask for Franzi Dunker regarding this opportunity. 

Apply for this job: CRA for mid size CRO

Contact Information:

Address:  Head Office
Victoria House
Consort Way
Tel:  01293 776644
Fax:  01293 822333

Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.