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A leading company is seeking a Freelance Clinical Research Associate (CRA) to provide operational support for clinical studies. Responsibilities include maintaining project documentation, supporting regulatory submissions, and ensuring compliance with GCP standards. The ideal candidate will have 4+ years of experience, strong communication skills, and proficiency in MS Office and eTMF systems.
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Freelance CRA / CRA Oversight / Clinical Consultant / CTM / MSL
CTA will support the Project Management work during the study
Responsibilities
Provide administrative and operational support to Clinical Operations
Maintain eTMF / ISF and support audit readiness
Assist with meeting coordination and minutes
Support regulatory submissions (CTIS), translations, and payments
Track study materials and team activities
Maintain project systems and ensure SOP / GCP compliance
Qualifications
Minimum 4 years of experience in a similar role
Background in administration or process management
Business-level fluency in English
Proficient in MS Office and eTMF systems
Strong communication and teamwork skills
Detail-oriented and able to meet deadlines
Seniority level
Employment type
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