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Clinical Research Associate

Role overview

Qualifications

  • College/University degree in Life Sciences or equivalent
  • At least 1 year of independent on-site monitoring experience
  • Full working proficiency in English and Serbian
  • Proficiency in MS Office applications

Responsibilities

  • Conduct and report onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management

Key facts

Hard skills

Other skills

  • Communication
  • Collaboration
  • Problem Solving
  • Multitasking

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

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Job description

Company Description

PSI is a leading Contract Research Organization with more than 30 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
  • Support and participate in audits and inspections

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • At least 1 year of independent on-site monitoring experience
  • Experience in all types of monitoring visits
  • Full working proficiency in English and Serbian
  • 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 across the region
  • Valid driver’s license

Additional Information

What We Offer:

  • Stability, long-term cooperation
  • Permanent contract, full-time job
  • Remote work setting
  • Car allowance, laptop and mobile phone
  • Career development 
  • Unique combination of team collaboration and independent work
  • Friendly and supportive colleagues
  • Onboarding courses about clinical research industry
  • Mentoring and on-the job training
  • Comfortable office and team support in Banja Luka

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

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MR

Marcus Rivera

Chief Revenue Officer

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