Type: office based

Are you an experienced CRA, 1-2 year of experience seeking to progress in your career within clinical research faster? Do you strive for more responsibilities and are looking for a company where every worker is counted? Well, our client is a leading global drug development company known for its excellence in the market place. As a result of rapid expansion a highly valued position of the CRAII – has become available. The company is constantly growing, so there are sound career prospects.

Your key responsibilities will include but not limited to:

Provision of submissions/approvals, feasibility, site initiation, selection, monitoring and close out visits for clinical studies. You will conduct full cycle of CRA activities in compliance with international ICH/GCP standards and will extensively use SOP regulations. Being involved in liaison with investigators and sponsors you will be responsible for reporting on all protocol or clinical study related issues to your project/line manager. Training/mentoring and co-monitoring of less experienced CRAs will also be a part of your duties.

Your profile

Degree in life science, pharma or/and medicine in clinical research. Demonstrated experience in Monitoring Clinical Trials. Excellent interpersonal, communication and leadership skills will be required to provide liaison at all levels internally and externally. Drive for success, results oriented mindset and ability to learn fast and work under pressure. Fluency in English and German is essential. If this role for some reason does not suit you, but you know someone suitable there is a bonus fee of EUR 250 for every referred candidate we successfully place.

In return our client will offer excellent career progression opportunities, competitive salary and remuneration package and an enviable working environment.