Remote In-House Clinical Research Associate I

Worldwide Clinical Trials; United States; Remote; USD 60,000 - 85,000; Full time

Job summary

Worldwide Clinical Trials is seeking an In-House Clinical Research Associate I to support delivery of clinical studies, ensuring GCP compliance and regulatory alignment.

This remote role welcomes candidates in Serbia, Spain or Poland and requires fluent English plus one additional language from French, German, Italian or Spanish.

You will collaborate with Clinical Trial Managers, site staff and cross-functional teams to maintain study quality, timely milestones, and robust trial documentation.

Qualifications

• Bachelor's degree in a medical/biological/related field or equivalent experience.
• Clinical research experience in roles such as Study Coordinator or CRA.
• Basic understanding of GCP and regulatory requirements.
• Familiarity with FDA/ICH regulations and local guidelines.
• Experience with EDC/eCRF/IVRS systems is preferred.
• Strong organizational and communication skills; MS Office proficiency.
• Fluent English plus one additional language (French/German/Italian/Spanish).

Responsibilities

• Support site start-up activities and essential document management.
• Maintain TMF/Study documentation with accuracy and compliance.
• Assist with Investigator Site File maintenance and quality checks.
• Conduct remote monitoring and support study visits under guidance.
• Build relationships with investigative sites through regular communication.
• Review EDC data entry, assist with query resolution and tracking.
• Generate reports and provide updates to Clinical Trial Managers.
• Support site staff management, regulatory documents, and delegation tracking.

Skills

Bachelor's degree

Clinical research experience

GCP knowledge

FDA/ICH regulations

EDC/eCRF/IVRS understanding

MS Office proficiency

English + second language

Education

Bachelor's degree in medical/biological/related field

Tools

EDC systems

eCRF

IVRS

Job description

Worldwide Clinical Trials is seeking an In-House Clinical Research Associate I to support delivery of clinical studies, ensuring GCP compliance and regulatory alignment.

This remote role welcomes candidates in Serbia, Spain or Poland and requires fluent English plus one additional language from French, German, Italian or Spanish.

You will collaborate with Clinical Trial Managers, site staff and cross-functional teams to maintain study quality, timely milestones, and robust trial documentation.