Clinical Research Associate

Actalent; Nordrhein-Westfalen; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

Actalent is seeking an experienced Clinical Research Associate to oversee one project during the routine monitoring and recruitment phase in Germany. This freelance position requires coordination with Ethics Committees and Regulatory Authorities, site management, and sponsor communications.

The role involves on-site and remote monitoring, close-out visits, and ensuring data quality for international audits, with support provided to the Clinical Team Manager across projects.

Qualifications

• Bachelor’s degree in Life Science.
• 5–10 years of clinical monitoring experience.
• Fluent in German and English.

Responsibilities

• Ongoing Ethics Committee and Regulatory Authority communication
• Monitoring and Close-out visits (on-site and remote)
• Investigator site management and communication
• Sponsor communication and training
• Responsible for ensuring that data will pass international quality assurance audits
• Give support to the Clinical Team Manager on different projects

Skills

Clinical monitoring

Regulatory communications

Sponsor communication

Site management

Remote monitoring

Education

Bachelor’s degree in Life Science

Job description

Our client, a multinational pharmaceutical company, is currently looking for an experienced Clinical Research Associate to take over one project during the routine monitoring and recruitment phase in Germany (freelancing).

Main responsibilities:

• Ongoing Ethics Committee and Regulatory Authority communication
• Monitoring and Close-out visits (on-site and remote)
• Investigator site management and communication
• Sponsor communication and training
• Responsible for ensuring that data will pass international quality assurance audits
• Give support to the Clinical Team Manager on different projects

Requirements:

• Bachelor’s degree (within Life Science field)
• 5 to 10 years in clinical monitoring experience
• German and English fluent