Clinical Research Associate II / Senior Clinical Research Associate Large Pharma/Biotech
On-siteFrankfurt am Main, Hesse, Germany
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams to ensure timely data collection and reporting while providing training to site staff. Build effective relationships with site personnel and stakeholders to facilitate smooth operations. Manage multiple sites and projects simultaneously with proficiency in clinical trial software. Requires 2+ years of CRA experience, German and English fluency, and 60% travel capability.
Required Qualifications
- Master or Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- Excellent communication skills in German and English
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
- Ability to travel at least 60% of the time (international (DACH region) and domestic - fly and drive)
- Valid driver's license
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
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