Are you interested in collaborating with leading pharma companies to help patients all around the world?

In our Clinical Functional Service Partnership models, we work in a close partnership with key customers in order to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single pharma client and gain direct and in-depth experience of collaborating with this sponsor.

Beside establishing strong relationships with the client and the involved investigators, you will conduct monitoring on complex clinical trials and assure the adherence to good clinical practices, standard operating procedures, and study protocols.

Responsibilities include:

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation

• Supporting the development of a subject recruitment plan

• Establishing regular lines of communication plus administering protocol and related study training to assigned sites

• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate

• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

We believe in hiring the best clinical talent in the industry.

Applicants should have:

• A Bachelor's degree in a health care or other scientific discipline or educational equivalent

• At least one year of on-site monitoring experience

• Alternatively, you should have an equivalent combination of education, training and experience

• Fluent written and verbal communication skills including good command of German and English language (at least C1 Level)

• Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

• Knowledge of applicable protocol requirements as provided in company training

• Availability to travel 40-60% of the working time

What you can expect:

• Resources that promote your career growth

• Leaders that support flexible work schedules

• Programs to help you build your therapeutic knowledge

• Dynamic work environments that expose you to new experiences

• Home-office, company car, accident insurance and more

• Salary starting from 50000 EUR brutto yearly, depending on experience

Due to the international scope of our business please apply with English version CV and your certificates and reference letters.