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SSU & Regulatory Coordinator – Italian, Czech or Hungarian Language
Syneos Health. Support timely preparation and execution of Confidentiality Disclosure Agreements (CDAs), Clinical Study Agreements (CSAs), associated budgets, and vendor agreements .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical study contracting processes, including the preparation and execution of Confidentiality Disclosure Agreements (CDAs) and Clinical Study Agreements (CSAs). Proficient in customizing templates, managing logistics, and tracking key performance indicators in compliance with global and local Standard Operating Procedures.
Highest-signal resume keywords
Clinical Study ContractingConfidentiality Disclosure Agreements (CDAs)Clinical Study Agreements (CSAs)Document Filing According to SOPsKPI Tracking
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
CDA CustomizationCSA CustomizationLogistics ManagementDocument FilingKPI TrackingProcess Improvement Communication
Industry Keywords
Standard Operating ProceduresSite IntelligencePlaybooksTemplatesClinical Study Agreements
About the role
Key responsibilities & impact- Support timely preparation and execution of Confidentiality Disclosure Agreements (CDAs), Clinical Study Agreements (CSAs), associated budgets, and vendor agreements
- Customize appropriate country CDA and CSA templates for clinical studies
- Manage logistics of obtaining internal and site signatures
- File documents according to global and local Standard Operating Procedures
- Track CDAs, CSAs, Site Intelligence, and KPIs/Metrics
- Provide input into updates to Playbooks and Templates
- Communicate potential clinical contracting process improvements to legal teams
Requirements
What you’ll need- Italian, Czech or Hungarian language
- Equivalent experience, skills, and/or education will also be considered
- Ability to support clinical study contracting processes and related documentation
- Ability to customize country CDA and CSA templates
- Ability to manage internal and site signature logistics
- Ability to file documents according to global and local Standard Operating Procedures
- Ability to track CDAs, CSAs, Site Intelligence, and KPIs/Metrics
- Ability to provide input on Playbooks and Templates and communicate potential process improvements with legal teams
Benefits
Comp & perks- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition
- Total rewards program
- Inclusive culture
- Reasonable accommodations when appropriate for employees or applicants with disabilities