Aktualnie prowadzone rekrutacje

With offices in Berlin, Warsaw and Prague, KCR Placement is an international boutique provider of ‘fit for purpose’ resourcing solutions for a wide array of functions, including expert, managerial and senior executive ones. We specialize in finding the right talents for Pharmaceutical, Biotech, Medical Device companies and Contract Research Organizations across Europe. 

We're onboarding best-in-class candidates, so give us a chance to meet you!

Current Vacancy Highlights:

(Senior) Clinical Research Associate / USA

We are currently seeking to employ a (Senior) Clinical Research Associate in Boston area. The  successful candidate will have the opportunity to be part of a rapidly growing CRO and a team of professional employees that care about the work they are involved in.


(Senior) Clinical Research Associate


You are an important part of the team. Grow with us and become an expert who is challenged, stimulated and engaged in projects for drug innovations. Your ideas and contributions are of great value. Your voice is heard. Join us and share our values: knowledge, customer focus, accountability, commitment, tenacity and determination to succeed. Have a real impact on company operations. We will encourage and support your development as a clinical research professional with comprehensive training programs and skillful guidance.
Location: United States
Type of Contract: Permanent, home-based
Seniority: Associate


Duties associated with the role:

  • Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines
  • Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
  • Reviews and verifies accuracy of clinical trial data collected
  • Provides regular site status information to team members
  • Performs source document verification and query resolution
  • Assesses IP accountability, dispensation, and compliance at the investigative sites
  • Verifies Serious Adverse Event (SAE) reporting according to trial specifications and ICHGCP guidelines
  • Updates applicable tracking systems

Desired Skills and Experience:

  • Bachelor’s Degree in Life Sciences or Healthcare
  • 3+ years of clinical research experience (CRO, Pharmaceutical, Biotechnology and/or healthcare setting)
  • 3+ years of site management and field monitoring experience
  • Up-to-date knowledge of legislation and regulations and ICH-GCP guidelines
  • Proficient in Microsoft Word, Excel, PowerPoint; eCRF and IVRS, project management tools
  • Experience in oncology would be a strong asset
  • Familiarity with advanced concepts of clinical research coupled with ability to work effectively in a team/matrix environment
  • Excellent written, verbal, and presentation skills
  • Thorough knowledge of ICHGCP, applicable regulations and monitoring practices
  • Strong team-player
We’re onboarding “best in class” candidates, so give us a chance to meet you!


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