Clinical Research Associate – Part-Time
Thermo Fisher Scientific
part-time
Posted on:
Location Type: Hybrid
Location: Karlsruhe • Germany
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Tech Stack
About the role
- Performs and coordinates all aspects of the clinical monitoring and site management process.
- Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.
- Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
- Ensures audit readiness.
- Develops collaborative relationships with investigational sites.
- Travel up to 50-75%.
Requirements
- Bachelor's degree in a life sciences related field or equivalent and relevant formal academic / vocational qualification.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
- Valid driver's license
- Full Right to work in Germany
- Fluency in English and German language to at least C1 level.
Benefits
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical monitoringsite managementprotocol complianceregulatory compliancedocumentation managementaudit readinessICH-GCP guidelinesSOPsdata reliabilityinvestigational site management
Soft skills
collaborative relationshipsinterpersonal skillscommunication skillsorganizational skills
Certifications
Bachelor's degree in life sciencesvalid driver's license