Clinical Research Associate (CRA)

We are looking for an experienced and committed CRA with great communication skills, critical thinking and attention to detail.

You will be responsible for monitoring clinical trials and ensuring that:
- Clinical Trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol.
- Data quality and integrity meet acceptable clinical standards.
- Rights and safety of patients involved in a study are protected.

You will also serve as facilitator of Clinical Trial conduct in respective area (country) in terms of identifying qualified sites and investigators, facilitating communication between Sponsor and regulatory authorities and trial sites.

We are an equal opportunities employer, in terms of gender and age. We create family friendly environment offering flexible working time, home based work.
Our CRAs have generally only 1 or 2 projects assigned and the travel time is limited to 40% of working time.

Other employee benefits will be specified during job interview.

A successful candidate must have:
Knowledge of clinical research processes and medical terminology.
Expert knowledge of ICH GCP and Regulatory requirements.
3-5 years of experience in clinical trial industry on a position of CRA - experience with oncology trials is much preferred.
Willingness and ability to travel domestically and internationally, as required.