Join IQVIA Biotech as a Clinical Research Associate 2 / CRA 2 to work home-based throughout Germany.

Your responsibilities will include:

Performing site selection, initiation, monitoring and close-out visits
Supporting the development of a subject recruitment plan
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Collaborating with experts at study sites and with client representatives
Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included
Besides focusing on projects in Germany, there may be the opportunity to gain experience in Austria or Switzerland.

Qualifications:

University Degree in life science or other scientific discipline or apprenticeship in the health care field
Minimum of two years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
Knowledge of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Strong written and verbal communication skills, attention to detail and ability to work in a fast-paced environment
Fluency in German on at least C1 level and a good command of English
Flexibility to conduct business travel up to about 40-60% of working time
Driver's license class B

What you can expect:

Clinical Research Associate 2 / CRA 2

Skills