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JOB DETAILS

Clinical Research Associate II

CompanyPSI CRO
LocationVienna
Work ModeOn Site
PostedSeptember 1, 2026
About The Company
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
About the Role

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 3,000 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

We are looking for a Clinical Research Associate to join a highly motivated, international team where collaboration, ownership, and trust are part of everyday work.

Hybrid role in Vienna

You will:

  • Conduct and report all types of onsite monitoring visits as well as remote visits.
  • Perform CRF review, source document verification and query resolution.
  • Be responsible for site communication and management.
  • Be involved in site identification process.
  • Assist in training of less expert CRAs, depending on your level of experience.

What makes the role different:

  • You will use your managerial skills to take a lead for assigned studies, having true ownership rather than simply monitoring tasks.
  • You will work across multiple sponsors and broad therapeutic areas, keeping your work varied and scientifically engaging.
  • You will work on fewer protocols, enabling deeper study focus and stronger site relationships across Austria.
  • You will work on complex and scientifically interesting trials.
  • You will join a setup where CRAs are trusted with responsibility and autonomy.

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Austria
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases, Multiple Sclerosis is a plus
  • Full working proficiency in English and German
  • 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 and valid driver’s license

Additional Information

As a privately owned mid-sized CRO, we are growing steadily and sustainably — with a strong focus on quality delivery, people, and long-term development. That means decisions are made close to the work, with real attention to what matters: patients, studies, and the people running them.

Why join us?

You will be part of an experienced, dynamic, and truly international team, where knowledge sharing and collaboration happen naturally across borders. You are not a number here — your contribution is visible, valued, and directly connected to study success.

We invest in structured onboarding and continuous mentoring, ensuring you are supported from day one and set up for long-term success. Many of our leaders today started in CRA roles internally — career progression is not an exception, but a well-established path.

You will work in a technologically integrated environment, with in-house systems designed to reduce administrative burden and keep your focus where it belongs: on high-quality site management and patient safety.

    What you can expect:

    • Excellent working conditions
    • Extensive training and friendly team
    • Opportunities for personal and professional growth
    • A fair and attractive salary and benefits package starting at EUR 60.000 gross (full-time basis) in accordance with the applicable Austrian collective agreement. The actual compensation package will be determined based on qualifications and relevant professional experience, with the possibility of a competitive overpayment above the collective agreement minimum.

    If you are looking for a role where you can grow professionally, take ownership early, and be part of a supportive and highly capable team, we would be happy to receive your application.

    Key Skills
    Clinical monitoringCRF reviewSource document verificationQuery resolutionSite managementSite identificationOncologyHematologyMS OfficeCommunicationCollaborationProblem-solvingProject managementClinical research
    Categories
    HealthcareScience & ResearchManagement & Leadership
    Benefits
    Structured onboardingContinuous mentoringProfessional development opportunitiesCompetitive salary
    Job Information
    📋Core Responsibilities
    You will conduct onsite and remote monitoring visits, perform source document verification, and manage site communications. Additionally, you will lead assigned studies, assist in training junior staff, and ensure high-quality site management.
    📋Job Type
    full time
    📊Experience Level
    2-5
    💼Company Size
    2956
    📊Visa Sponsorship
    No
    💼Language
    English
    🏢Working Hours
    40 hours
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