
10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
🔥 54 minutes ago
🗣️🇮🇹 Italian Required
🗣️🇨🇿 Czech Required
🗣️🇭🇺 Hungarian Required
Where this job comes from
Posted on Syneos Health's careers page, not through a job board
First seen by Remote Rocketship 54 minutes ago

10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
• 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
• 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
• 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
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