Clinical Research Associate II

Psi CRO; Wien; Hybrid; EUR 54.000 - 66.000; Vollzeit

Zusammenfassung

Psi CRO in Austria is seeking a Clinical Research Associate to join a highly motivated, international team where collaboration, ownership, and trust are central to our work.

You will conduct on-site and remote monitoring visits, perform CRF review and source data verification, manage site communications, participate in site identification, and help train less experienced CRAs, with room to take ownership across multiple studies.

Qualifikationen

• College/University degree in Life Sciences or equivalent.
• Independent on-site monitoring experience in Austria.
• Experience in Phase II and/or III monitoring visits.
• Experience in Oncology, Hematology, Infectious/Rare/GI diseases is a plus.
• Full working proficiency in English and German.
• Proficiency in MS Office applications.
• Ability to travel and hold a valid driver’s license.

Aufgaben

• Conduct and report all types of onsite monitoring visits as well as remote visits.
• Perform CRF review, source data 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.

Kenntnisse

On-site monitoring

German language

English language

MS Office

Travel willingness

Communication skills

Ausbildung

Life Sciences degree

Jobbeschreibung

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.

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 inOncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases, Multiple Sclerosisis 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.

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.

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