For our client, an internationally recognized full-service CRO for dermatological product development, we are currently searching for a Lead Clinical Research Associate to join the team at the clients headquarters in Hamburg, Germany.

The main task of the position is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house or in the Northern German region.

Lead Clinical Research Associate (f/m/d) - homebased

Key Responsibilities:

• Perform monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoring
• Generation and updating of monitoring plans and site initiation presentation
• Evaluating the quality and integrity of site practices
• Act as contact for clinical trial suppliers and other vendors as assigned
• Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols
• Close cooperation with the different departments in-house as well as freelance CRAs
• Compliance with protocol, GCP/ICH Guidelines

Required Qualifications:

• 4 years of clinical monitoring experience (preferred Dermatology)
• Degree in a scientific or medical discipline or equivalent
• Very good knowledge of Good Clinical Practice/ICH Guidelines
• Proven ability to work independently in a fast-paced environment
• Excellent communication, interpersonal, and organizational skills
• Fluency in German and a high level of English language

Your contact:

Sibel Atilgan

Recruitment Consultant - Clinical Research Pharma & Biotech

Telefon: +49 89 5519 7739

E-Mail:s.atilgan(at)progressive.de