IQVIA
Regulatory and Start Up Specialist(m/w/x)
Full-timeWith HomeofficeExperienced
Basel
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IQIQVIA
Sr. Site Activation Specialist(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Clinical trial site activation and contract negotiation for life sciences. University degree and 5+ years of clinical research experience required. Bonus system, pension, and supportive teams.
Requirements
- University degree in life science or scientific discipline, or healthcare apprenticeship or 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 task prioritization
Tasks
- Perform clinical research site activation activities
- Serve as Single Point of Contact for assigned studies
- Ensure adherence to SOPs, work instructions, and project timelines
- Perform regulatory, start-up, and maintenance activities
- Review, prepare, and negotiate site contracts and budgets
- Prepare and review site regulatory documents for completeness
- Perform quality control on documents provided by sites
- Complete and submit approval request documents to regulatory and ethical committees
- Ensure regulatory documents and approvals are granted
- Ensure IP Release is authorized
- Complete specific project deliverables
- Track and follow up on document progress and approvals
- Maintain internal systems, databases, and tracking tools
- 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
- Supportive teams
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
Flexible Working
- Flexible working schedule
- Home-office
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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IQIQVIA
Sr. Site Activation Specialist(m/w/x)
Basel
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Clinical trial site activation and contract negotiation for life sciences. University degree and 5+ years of clinical research experience required. Bonus system, pension, and supportive teams.
Requirements
- University degree in life science or scientific discipline, or healthcare apprenticeship or 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 task prioritization
Tasks
- Perform clinical research site activation activities
- Serve as Single Point of Contact for assigned studies
- Ensure adherence to SOPs, work instructions, and project timelines
- Perform regulatory, start-up, and maintenance activities
- Review, prepare, and negotiate site contracts and budgets
- Prepare and review site regulatory documents for completeness
- Perform quality control on documents provided by sites
- Complete and submit approval request documents to regulatory and ethical committees
- Ensure regulatory documents and approvals are granted
- Ensure IP Release is authorized
- Complete specific project deliverables
- Track and follow up on document progress and approvals
- Maintain internal systems, databases, and tracking tools
- 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
- Supportive teams
Career Advancement
- Career growth resources
Startup Environment
- Dynamic work environments
Flexible Working
- Flexible working schedule
- Home-office
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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.
Not a perfect match?
- IQVIA
Regulatory and Start Up Specialist(m/w/x)
Full-timeWith HomeofficeExperiencedBasel - IQVIA
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Senior Clinical Research Associate(m/w/x)
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