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Job Details

Clinical Research Associate 2 (CRA2)

Company: PAREXEL
Location: Amsterdam office based, or home based in Middle NL
Reference: 40180
Closing Date: 14 Dec 17
Type: Full Time
Salary (£): Competitive
Benefits: Competitive, ask for our holiday package

Job Summary:

PAREXEL Netherlands is searching for a CRA to join their team in Amsterdam. Are you fluent in Dutch, do you value work-life balance in your career as a CRA, would you like to work in a great team where you are valued as a person next to your skills? Please get in touch!

Requirements:

There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

That’s PAREXEL. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor. ↵

At PAREXEL, we believe that the power to work independently and intelligently should be yours every day.

Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world. PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities.

YOUR KEY ACCOUNTABILITIES:

  • Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
  • Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
  • Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
  • Good knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Function as a mentor and role model for other CRA team members

YOUR SKILLSET:

  • Minimum 2 years of monitoring experience in clinical research
  • Educated to degree level (biological science, pharmacy or other health related discipline)
  • Strong working knowledge of EDC systems and IVRS
  • Experience of CTMS preferred
  • Competent in written and oral English and Dutch

OUR OFFER:

We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research.

You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.

If you are ready to join PAREXEL’s Journey, please apply!

Apply for this job: Clinical Research Associate 2 (CRA2)

Contact Information:

Address:  PAREXEL International
The Quays
101-105 Oxford Road
Uxbridge
Middlesex
UB8 1LZ
England
Tel:  +44 1895 238000
Fax:  +44 1895 238494
Website:  Visit Our Web Site
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