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Sr. Site Activation Specialist(m/w/x)
Site activation for clinical trials, serving as single point of contact for studies. University degree in life science or equivalent experience required. Bonus system, pension, and supportive leaders.
Requirements
- University degree in life science or scientific discipline, or apprenticeship in health care or as legal secretary/paralegal
- Clinical research experience, preferable in study start-up, or equivalent education/training/experience
- Knowledge of GCP and ICH guidelines
- Fluent German (C1 level) and good English command
- Strong written and verbal communication skills
- Attention to detail and ability to prioritize tasks
Tasks
- Perform clinical research site activation activities
- Serve as Single Point of Contact for assigned studies
- Ensure adherence to SOPs and project timelines
- Perform regulatory, start-up, and maintenance activities
- Review and prepare site contracts and budgets
- Prepare and review site regulatory documents
- Perform quality control on site documents
- Submit approval request documents to regulatory and ethical committees
- Ensure regulatory approvals and IP Release authorization
- Track and follow up on document progress
- Maintain internal systems and databases with project information
- Review and establish project planning and timelines
- Ensure project efficiency and adherence to timelines
- Implement monitoring measures and contingency plans
- Review and provide feedback on site performance metrics
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Bonuses & Incentives
- Bonus system
Retirement Plans
- Pension
Mentorship & Coaching
- Supportive leaders
- Mentors
Team Events
- Teams
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
Flexible Working
- Flexible working schedule
- Home-office
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Sr. Site Activation Specialist(m/w/x)
Site activation for clinical trials, serving as single point of contact for studies. University degree in life science or equivalent experience required. Bonus system, pension, and supportive leaders.
Requirements
- University degree in life science or scientific discipline, or apprenticeship in health care or as legal secretary/paralegal
- Clinical research experience, preferable in study start-up, or equivalent education/training/experience
- Knowledge of GCP and ICH guidelines
- Fluent German (C1 level) and good English command
- Strong written and verbal communication skills
- Attention to detail and ability to prioritize tasks
Tasks
- Perform clinical research site activation activities
- Serve as Single Point of Contact for assigned studies
- Ensure adherence to SOPs and project timelines
- Perform regulatory, start-up, and maintenance activities
- Review and prepare site contracts and budgets
- Prepare and review site regulatory documents
- Perform quality control on site documents
- Submit approval request documents to regulatory and ethical committees
- Ensure regulatory approvals and IP Release authorization
- Track and follow up on document progress
- Maintain internal systems and databases with project information
- Review and establish project planning and timelines
- Ensure project efficiency and adherence to timelines
- Implement monitoring measures and contingency plans
- Review and provide feedback on site performance metrics
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Bonuses & Incentives
- Bonus system
Retirement Plans
- Pension
Mentorship & Coaching
- Supportive leaders
- Mentors
Team Events
- Teams
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
Flexible Working
- Flexible working schedule
- Home-office
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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