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Job Details

Enhance your expertise - Associate CRA opportunity (based in Warsaw, Poland)

Company: IQVIA
Location: Warsaw
Reference: 1807584
Closing Date: 21 Oct 18
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

If you are planning to continue your career as a CRA, this role is an ideal stepping-stone. You’ll receive training according to development plan and progress your career in the direction you choose. Moreover, you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. ...

Requirements:

If you are planning to continue your career as a CRA, this role is an ideal stepping-stone. You’ll receive training according to development plan and progress your career in the direction you choose. Moreover, you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

 

Award winning and innovative, we’ll give you access to cutting-edge in-house technology allowing you to work on global projects but with a regional / home state travel remit, so there is no need for national traveling. You’ll be building a smart and flexible career with no limits.

 

While projects vary, your typical responsibilities might include: 

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 

You should be comfortable with collaboration and communication with a variety of colleagues and customers. Ideally, you should have a good basic knowledge of applicable clinical research regulatory requirements.


 

You should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least 1 year of working experience in clinical trials as Sub-Investigator / Study Coordinator / Clinical Trials Assistant or similar role OR
  • At least three months of on-site monitoring experience OR
  • Successful completion of a CRA Trainee Program
  • Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Good written and verbal communication skills including good command of English language
  • Good organizational and problem-solving skills

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team. 

Connect to great opportunity™

 

IQVIA™ is a strong advocate of diversity and inclusion in the workplace.  We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success.  We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

Apply for this job: Enhance your expertise - Associate CRA opportunity (based in Warsaw, Poland)

Contact Information:

Address:  London Office
210 Pentonville Road London
N1 9JY
England
Tel:  +44 (0) 20 3075 5000
Website:  Visit Our Web Site

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