3 days ago

Clinical Trial Assistant - Sponsor Dedicated - Amsterdam

Syneos Health

Amsterdam

3 days ago

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Syneos Health seeks a Clinical Trial Assistant for a sponsor-dedicated role in Amsterdam. The position involves supporting clinical trial operations, managing study documentation, and facilitating communication among team members. Requires an associate degree in life sciences or related field and knowledge of GCP/ICH guidelines.

On-siteFull-timeEntry LevelGood Clinical Practice (GCP)ICH Guidelines

Clinical Trial Assistant - Sponsor Dedicated - Amsterdam

Apply

On-siteFull-timeEntry LevelGood Clinical Practice (GCP)

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

On-site

Employment Type

Full-time

Experience Level

Not Applicable

Core Qualifications

Technical (Must-have)

Good Clinical Practice (GCP)ICH GuidelinesMS Office ApplicationsOrganizational SkillsTime ManagementCommunication SkillsInterpersonal SkillsEnglish Language

Soft Skills

Organizational SkillsTime ManagementCommunicationInterpersonal SkillsAbility to Work Independently

Key Responsibilities

•Set-up, maintain and/or close out project files and study information on databases and systems.
•Attend, participate, prepare and distribute meeting minutes and action items for internal and external meetings.
•Maintain timely and effective communication among team members and site staff.
•Provide administrative support to Project Leads and functional leads.
•Ensure all study documents are archived based on appropriate guidelines and policy.
•Provide support for quality assurance activities, including preparation for audits and internal review.

Clinical Trial AssistantSponsor DedicatedAmsterdamSyneos HealthClinical ResearchGCPICH GuidelinesFull-timeOn-siteBiotechnology

Key Responsibilities

•Set-up, maintain and/or close out project files and study information on databases and systems.

•Attend, participate, prepare and distribute meeting minutes and action items for internal and external meetings.

•Maintain timely and effective communication among team members and site staff.

•Provide administrative support to Project Leads and functional leads.

•Ensure all study documents are archived based on appropriate guidelines and policy.

•Provide support for quality assurance activities, including preparation for audits and internal review.