Dein persönlicher KI-Karriere-Agent
Sr Clinical Project Support Specialist - Sponsor dedicated(m/w/x)
Supporting global clinical trials from planning to close-out, managing documentation and systems. Strong knowledge of GCP and ICH guidelines required. Work across rotating global sites, 5-person project teams.
Anforderungen
- University degree or comparable professional education
- Exceptional communication and stakeholder management skills
- Strong knowledge of GCP and ICH guidelines
- Excellent organizational and problem-solving skills
- Ability to work independently, prioritize tasks, and manage projects
- Experience in complex international environment
- Detail-oriented with strong commitment to quality and compliance
- Proficiency in MS Office and clinical trial systems/tools
- Fluent in written and spoken English
Aufgaben
- Support global clinical trials from planning to close-out
- Manage trial-related documentation and systems
- Ensure compliance with SOPs, ICH-GCP, and regulatory requirements
- Plan and coordinate trial activities across regions
- Maintain trial documentation (ISF, TMF, submissions)
- Collaborate with stakeholders, vendors, and trial teams
- Manage clinical trial systems and databases
- Prepare and distribute project plans and updates
- Monitor trial progress, budgets, and data
- Identify and implement corrective actions
- Coordinate documentation workflows and regulatory submissions
- Support trial close-out and deliverables preparation
- Coordinate logistics for trial meetings and supplies
- Contribute to quality oversight and best practices
- Act as a key point of contact for trial-related queries
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Tools & Technologien
- MS Office
- clinical trial systems/tools
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Sr Clinical Project Support Specialist - Sponsor dedicated(m/w/x)
Supporting global clinical trials from planning to close-out, managing documentation and systems. Strong knowledge of GCP and ICH guidelines required. Work across rotating global sites, 5-person project teams.
Anforderungen
- University degree or comparable professional education
- Exceptional communication and stakeholder management skills
- Strong knowledge of GCP and ICH guidelines
- Excellent organizational and problem-solving skills
- Ability to work independently, prioritize tasks, and manage projects
- Experience in complex international environment
- Detail-oriented with strong commitment to quality and compliance
- Proficiency in MS Office and clinical trial systems/tools
- Fluent in written and spoken English
Aufgaben
- Support global clinical trials from planning to close-out
- Manage trial-related documentation and systems
- Ensure compliance with SOPs, ICH-GCP, and regulatory requirements
- Plan and coordinate trial activities across regions
- Maintain trial documentation (ISF, TMF, submissions)
- Collaborate with stakeholders, vendors, and trial teams
- Manage clinical trial systems and databases
- Prepare and distribute project plans and updates
- Monitor trial progress, budgets, and data
- Identify and implement corrective actions
- Coordinate documentation workflows and regulatory submissions
- Support trial close-out and deliverables preparation
- Coordinate logistics for trial meetings and supplies
- Contribute to quality oversight and best practices
- Act as a key point of contact for trial-related queries
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Tools & Technologien
- MS Office
- clinical trial systems/tools
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
IQVIA
Branche
Healthcare
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Noch nicht perfekt?
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