Clinical Trial Operations Specialist

Parexel; United States; Vor Ort; USD 55.000 - 85.000; Vollzeit

Zusammenfassung

Parexel is seeking a Clinical Trial Coordinator to support the Clinical Research Manager and team through the study life cycle from startup to closure. You will manage documentation, regulatory activities, budgeting, and site communications in a global matrix environment.

The role requires strong organizational and communication skills, proficiency with MS Office, and the ability to work independently while collaborating with investigators and vendors.

Qualifikationen

• Bachelor’s degree in Life Sciences or equivalent healthcare experience.
• 1–2 years of Clinical Research experience preferred.
• Strong documentation and regulatory understanding.
• Excellent communication and time management abilities.

Aufgaben

• Support study life cycle from startup to closure.
• Track essential documents and safety reports; maintain study tools and trackers.
• Coordinate regulatory submissions and site start-up activities.
• Assist with trial master file maintenance and document revisions.
• Support budgeting, agreements, and payments processes.
• Plan and organize investigator meetings and other study-related meetings.

Kenntnisse

Fluent in Local Languages

Business English (verbal and written)

Communication skills

Time management

Organizational skills

Interpersonal skills

Independent working

Problem solving

Ausbildung

Bachelor’s degree (Life Sciences preferred) or healthcare equivalent

Tools

MS Office

Clinical IT applications

Electronic Trial Master File (eTMF)

Jobbeschreibung

Parexel is seeking a Clinical Trial Coordinator to support the Clinical Research Manager and team through the study life cycle from startup to closure. You will manage documentation, regulatory activities, budgeting, and site communications in a global matrix environment.

The role requires strong organizational and communication skills, proficiency with MS Office, and the ability to work independently while collaborating with investigators and vendors.