Hybrid Clinical Trials Coordinator (Remote-Ready)

Stryker Corporation

Netherlands

Hybrid

Confidential

Full time

13 days ago
Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

Stryker Corporation seeks a Clinial Trial Coordinator to support the execution of clinical studies across Europe. You will coordinate essential activities, maintain Trial Master Files, and partner with cross-functional teams to ensure compliance with GCP and regulatory requirements.

The role requires a Bachelor’s in Life Sciences, at least 2 years in clinical research, and proficiency with electronic trial systems. A hybrid work setup with travel expectations is possible.

Qualifications

  • Bachelor's degree in Life Sciences or a related field.
  • Minimum 2 years of experience in clinical research, trial administration, or study coordination.
  • Experience working with Good Clinical Practice (GCP) requirements.
  • Experience using electronic clinical trial systems, databases, or documentation management systems.

Responsibilities

  • Support clinical trial activities across the study lifecycle including site activation and closeout.
  • Coordinate Trial Master Files and ensure inspection readiness and regulatory compliance.
  • Prepare study meetings and track follow-up actions.
  • Review site-related documents and data for accuracy and completeness.
  • Manage study-related invoicing and payment tracking for sites and hospitals.
  • Develop and distribute study communications, reports, and newsletters.

Skills

Life Sciences
Clinical Research
GCP Knowledge

Education

Bachelor's degree in Life Sciences

Tools

Electronic Trial Systems

Job description

Stryker Corporation seeks a Clinial Trial Coordinator to support the execution of clinical studies across Europe. You will coordinate essential activities, maintain Trial Master Files, and partner with cross-functional teams to ensure compliance with GCP and regulatory requirements.

The role requires a Bachelor’s in Life Sciences, at least 2 years in clinical research, and proficiency with electronic trial systems. A hybrid work setup with travel expectations is possible.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Impactful European Clinical Trials Coordinator (Hybrid)
Impactful European Clinical Trials Coordinator (Hybrid)

Stryker • Maastricht

Hybrid
EUR 42,000 - 78,000
Incentive compensation
Comprehensive benefits
Global Clinical Trials Coordinator
Global Clinical Trials Coordinator

Stryker Group • Amsterdam

On-site
EUR 42,000 - 78,000
Clinical Study Coordinator
Clinical Study Coordinator

Stryker • Maastricht

Hybrid
EUR 42,000 - 78,000
Incentive compensation
Comprehensive benefits
Clinical Study Coordinator
Clinical Study Coordinator

Stryker Group • Amsterdam

On-site
EUR 42,000 - 78,000
Hybrid CRA: Lead Clinical Trials & Compliance
Hybrid CRA: Lead Clinical Trials & Compliance

GCP-Service International Ltd. & Co.KG • Nijmegen

On-site
EUR 55,000 - 75,000
Home office option
Office-based position in Nijmegen
Travel reimbursement
+2
Hybrid Clinical Research Project Coordinator
Hybrid Clinical Research Project Coordinator

NES Fircroft • Heerlen

Hybrid
EUR 25,000 - 32,000
Senior Field Clinical Research Engineer – EP Trials Europe
Senior Field Clinical Research Engineer – EP Trials Europe

Boston Scientific • Kerkrade

On-site
EUR 75,000 - 110,000
Project Coordinator
Project Coordinator

NES Fircroft • Heerlen

Hybrid
EUR 25,000 - 32,000
Global Clinical Trial Lead — Project Management
Global Clinical Trial Lead — Project Management

Syneos Health • Netherlands

Remote
EUR 85,000 - 110,000
Global Clinical Trial Lead — Project & Delivery
Global Clinical Trial Lead — Project & Delivery

Syneos Health • Netherlands

On-site
EUR 90,000 - 120,000