Senior Clinical Research Associate

Everest Clinical Research Services Inc

WarsawFull-timeMid LevelOn-site

Job Description

Everest has been a CRO since January 2004 with a strong foundation as a statistical, programming, and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Headquartered in Toronto, Canada, with subsidiary offices in New Jersey, USA; Shanghai, China; Taipei, Taiwan; Bulgaria, Romania, Poland, and Croatia in Europe.

Everest continues to deepen capabilities and serve highly satisfied customers in data/analytics services and full-service execution with quality, effectiveness, and agility for worldwide clinical trials.

Growing steadily over 21 years, Everest is a preferred vendor for 100+ active clients, including major, mid-sized, and small pharmaceutical, biotech, and medical device companies. We value our clients and all growth to date is primarily from their repeat and referral business. We are known for our high-touch approach with client teams, high quality standards, customer-focus, “can-do” culture, advanced technology utilization, and continuous improvement.

A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success. Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that’s us…that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our growing team in Warsaw, Poland as an experienced Clinical Research Associate (CRA). This is a full-time CRA position for a candidate with at least one year of monitoring experience. Job responsibilities will include site identification and site selection, performing regulatory and ethics committee submissions, monitoring for clinical studies, site management and local safety reporting, as needed.

Skills required include:

  • At least one year of clinical trials monitoring experience
  • University degree in life science
  • Excellent written and oral communication skills
  • Attention to detail
  • Good organizational and time management skills
  • Fluent in written and verbal English
  • Ability to work well within a team
  • Computer competency
  • Position requires up to 50%-60% travel
  • Posted 2 months ago

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