Clinical Research Associate I

PSI CROUS, US
$80,000 - $80,000Onsite

About The Position

As a Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Requirements

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Experience as a Study Coordinator (or similar role) is required
  • Full working proficiency in English
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability and willingness to travel frequently
  • Valid driver’s license

Nice To Haves

  • Experience working on Gastroenterology clinical trials preferred

Responsibilities

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup (if applicable)
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

Benefits

  • The company cares – for our staff, for our clients, for our partners and for the quality of the work we do.
  • dynamic, global company
  • work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
  • support of a knowledgeable and professional team.
  • develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.
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