Clinical Trial Associate: Study Coordination & Compliance

ICON Clinical Research; Österreich; Vor Ort; EUR 42.000 - 62.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee assistance programme

Zusammenfassung

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Qualifikationen

• Bachelor's degree in a scientific or healthcare-related field.
• Experience or strong interest in clinical research is required.
• Knowledge of clinical trial processes, regulations and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel up to 10%.

Aufgaben

• Assist in coordination and administration of clinical trials, ensuring protocol/regulatory compliance.
• Maintain and organize study files, essential documents, and regulatory submissions.
• Support preparation of informed consent forms and case report forms.
• Collaborate with cross-functional teams to facilitate trial execution.
• Contribute to tracking and reporting of trial metrics and milestones.

Kenntnisse

Excellent organizational and comms

Knowledge of clinical trial processes

Team collaboration in fast-paced env

Willingness to travel

Strong communication skills

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Jobbeschreibung

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.