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Site Activation Specialist(m/w/x)
Supporting clinical trial start-up and site management in the DACH region. Local regulatory understanding and 2-3+ years of site activation experience required. Hybrid work, focus on essential document management.
Requirements
- Experience in Switzerland or DACH region exposure
- Based in Germany with local regulatory understanding
- 2-3+ years site activation, study start-up, or clinical research experience
- Bachelor’s degree in Life Sciences or related field
- Solid knowledge of clinical trial start-up processes and regulatory requirements
- Experience managing site documentation and submission processes
- Strong attention to detail and ability to manage multiple sites and timelines
- Fluent German and English (written and spoken)
- Clinical studies in Switzerland or Swiss regulatory familiarity advantageous
- Cross-border (DACH) studies exposure advantageous
Tasks
- Support country-level clinical trial start-up and site management
- Act as primary point of contact for assigned investigative sites
- Execute feasibility, site identification, and site activation activities
- Prepare, review, and manage essential site and regulatory documents
- Support contract and budget processes with internal stakeholders
- Maintain and update tracking tools, timelines, and internal systems
- Monitor and report on site activation progress and performance metrics
- Ensure compliance with ICH-GCP, local regulations, and study requirements
- Collaborate with Site Activation Managers, Project Management, and cross-functional teams
Work Experience
- 2 - 3 years
Education
- Bachelor's degree
Languages
- German – Fluent
- English – Fluent
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Site Activation Specialist(m/w/x)
Supporting clinical trial start-up and site management in the DACH region. Local regulatory understanding and 2-3+ years of site activation experience required. Hybrid work, focus on essential document management.
Requirements
- Experience in Switzerland or DACH region exposure
- Based in Germany with local regulatory understanding
- 2-3+ years site activation, study start-up, or clinical research experience
- Bachelor’s degree in Life Sciences or related field
- Solid knowledge of clinical trial start-up processes and regulatory requirements
- Experience managing site documentation and submission processes
- Strong attention to detail and ability to manage multiple sites and timelines
- Fluent German and English (written and spoken)
- Clinical studies in Switzerland or Swiss regulatory familiarity advantageous
- Cross-border (DACH) studies exposure advantageous
Tasks
- Support country-level clinical trial start-up and site management
- Act as primary point of contact for assigned investigative sites
- Execute feasibility, site identification, and site activation activities
- Prepare, review, and manage essential site and regulatory documents
- Support contract and budget processes with internal stakeholders
- Maintain and update tracking tools, timelines, and internal systems
- Monitor and report on site activation progress and performance metrics
- Ensure compliance with ICH-GCP, local regulations, and study requirements
- Collaborate with Site Activation Managers, Project Management, and cross-functional teams
Work Experience
- 2 - 3 years
Education
- Bachelor's degree
Languages
- German – Fluent
- English – Fluent
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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