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Contract Clinical Research Associate

Role overview

Qualifications

  • College/University degree in Life Sciences or equivalent
  • Independent monitoring experience in Lithuania
  • Full working proficiency in English and Lithuanian
  • Proficiency in MS Office applications

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

Other skills

  • Microsoft Office
  • Communication
  • Collaboration
  • Problem Solving
  • Planning
  • 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 β€˜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

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Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

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.

Remote opportunity in Lithuania

You will:

  • 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
  • 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 monitoring experience in Lithuania, preferably on contractor/freelance position
  • Full working proficiency in English and Lithuanian
  • Knowlegde of Latvian is a plus
  • 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
  • Valid driver's license

Additional Information

We offer:

  • Flexible working conditions
  • Extensive training and friendly team
  • Opportunities for personal and professional growth
  • Competitive salary starting at 45 euro per hour. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.

If you feel it is time to make your skills and knowledge visible within a company with true focus on its people, then PSI CRO is the right choice for you.

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MR

Marcus Rivera

Chief Revenue Officer

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