Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

CLINICAL RESEARCH ASSOCIATE (CRA) - United Kingdom

Company: PRA Health Sciences
Location: Reading, United Kingdom
Reference: RP-2017-42606
Closing Date: 10 Dec 17
Type: Full Time
Salary (£): Competitive
Benefits: Excellent Salary and Benefits

Job Summary:

An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Clinical Research Associate (CRA) and help realize your career potential.

Requirements:

CLINICAL RESEARCH ASSOCIATE (CRA)

Location: Reading,United Kingdom

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

For more information please see our website: www.prahs.com

Responsibilities:

  • Applies knowledge of PRA’s policies and procedures
  • Demonstrates excellent written and oral communication
  • Demonstrates excellent knowledge of ICH/GCP
  • Displays ability to manage investigative sites to facilitate trial deliverables
  • Demonstrates ability to escalate issues appropriately 
  • Conducts monitoring to confirm subject safety and data ntegrity
  • Describes and demonstrates the principals of IP accountability
  • Identifies scientific misconduct at the site level
  • Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platforms
  • Mentors CRAs new to the position or company
  • Serves as an observation visit leader
  • Conducts monitoring evaluation visits
  • Assists team lead in the development of trial tools or documents
  • Assists with CTM tasks
  • Participates in the development of process changes/improvements
  • Presents at client meetings/Investigator meetings
  • Provides training to trial teams

Desired skills and qualifications:

  • Read, write and speak fluent English; fluent in host country language required.
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • 5+ years of clinical monitoring experience required
  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • An advanced degree (e.g., M.S., M.B.A., PharmD, etc)
  • Experience in monitoring complex trials
  • Participation in departmental initiatives

Together with a competitive salary, we offer a comprehensive range of benefits and an excellent working environment. As we continue to expand, there will be career opportunities on a truly global scale.

If you have any questions please email recruiteruk@prahs.com or call our recruitment department at +44 (0) 1189 213098
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities

Apply for this job: CLINICAL RESEARCH ASSOCIATE (CRA) -  United Kingdom

Contact Information:

Address:  Head Office
500 South Oak Way
Green Park
Reading
Berkshire
RG2 6AD
England
Tel:  +44 (118) 918 1000
Fax:  +44 (118) 918 1001
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.