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Clinical Research Associate II

PSI CRO AG

Role overview

Qualifications

  • College/University degree in Life Sciences or equivalent
  • Independent on-site monitoring experience in France
  • Experience in Phase II and/or III monitoring visits
  • Full working proficiency in English

Responsibilities

  • Conduct and report all types of onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Support regulatory team in preparing documents for study submissions

Key facts

Hard skills

Oncology Clinical Research Source Document Query Planning Infectious Disease Nursing

Other skills

  • Communication
  • Collaboration
  • Problem Solving
  • Multitasking
  • Teamwork

About the company

PSI CRO AG logo

PSI CRO AG

Contract Research Organizations (CRO)

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

Links

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Job description

Company Description

PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • 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

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in France
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in oncology, hemophilia, infectious diseases, GI
  • Full working proficiency in English 
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

We offer:         

  • Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
  • Development opportunities across PSI departments
  • Flexible working hours
  • Home-office option available, as well as combination of home and office work arrangement
  • Extensive onboarding trainings and professional development training programs
  • Highly developed company culture and positive team atmosphere
  • Additional leave days (12 days of RTT)
  • Please submit your CV/resume in English

 

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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