Clinical Research Associate II at PSI CRO

Vienna, , Austria -

Full Time

Start Date

Immediate

Expiry Date

05 May, 26

Salary

62000.0

Posted On

04 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Monitoring, CRF Review, Source Document Verification, Query Resolution, Communication, Relationship Management, Training, Multitasking, Organizational Skills, Problem-Solving, Planning, Collaboration, Customer Service, Oncology, Hematology, Infectious Diseases

Industry

Pharmaceutical Manufacturing

Description

Company Description We are a company that cares —about our staff, our clients, our partners, and the quality of the work we do. Founded in 1995, we are a dynamic global organization with more than 3,000 driven, dedicated, and passionate professionals. At the forefront of medical science, we are committed to changing lives and bringing new medicines to those who need them most. Our work environment values collaboration, innovation, and excellence, making every team member’s contribution meaningful. Job Description As a Clinical Research Associate, you will take on a variety of monitoring tasks and contribute to clinical studies across multiple therapeutic areas. You will ensure the highest quality standards in the industry while delivering exceptional customer service. Office-based in Vienna Key Responsibilities: Conduct and report all types of onsite monitoring visits as well as remote visits. Perform CRF review, source document verification, and query resolution. Manage communication and relationship with clinical sites. Participate in the site identification process. Support the training and mentoring of less experienced CRAs, depending on your level of expertise. Qualifications College or university degree in Life Sciences, or an equivalent combination of education, training, and experience. Independent on-site monitoring experience within Austria. Experience conducting all types of monitoring visits in Phase II and/or Phase III clinical trials. Experience in Oncology, Hematology, Infectious/Rare/Gastrointestinal Diseases, or Multiple Sclerosis is a plus. Full professional proficiency in English and German. Proficiency in MS Office applications. Strong planning, multitasking, and organizational skills; able to work effectively in a dynamic team environment. Excellent communication, collaboration, and problem-solving skills. Willingness and ability to travel as required. Valid driver’s license. Additional Information Make the right move and elevate your career to the next level. Join a company that values its people and invests in their professional growth, development, and long-term success. Be part of a team where your contributions truly make a difference. We Offer: Excellent working conditions in a supportive and collaborative environment. Extensive training and a friendly, professional team. Opportunities for personal and professional growth. A fair and attractive salary and benefits package starting at EUR 62,000 gross, with the final salary determined individually based on qualifications and experience.

Responsibilities

Conduct and report all types of onsite monitoring visits as well as remote visits. Manage communication and relationship with clinical sites while ensuring high-quality standards in clinical studies.