As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.
Your responsibilities will include:
- Conducting and reporting all types of onsite monitoring visits
- Driving the study startup phase (if applicable)
- Performing CRF reviews, source document verification and query resolution
- Be responsible for site communication and management
- Supervising study activities, timelines and schedules for each site
- Acting as a point of contact for in-house support services and vendors
- Supporting quality control, such as compliance monitoring and reports review
- Participating in feasibility research
- Assisting in training of less experienced CRAs
- 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
What We Offer:
- Stability, long-term cooperation
- Permanent contract, full-time job
- Hybrid or home-based work setting
- Competitive salary and benefit package
- 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 and well-established modern office
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
