RA Executive FDF Dossiers

• Manage and maintain accurate records of clinical trial data.
• Coordinate with cross-functional teams to ensure timely completion of studies.
• Develop and implement effective study protocols and case report forms.
• Conduct site visits to monitor progress and ensure compliance with regulations.
• Collaborate with stakeholders to resolve issues and improve processes.
• Ensure data quality and integrity through regular audits and reviews.

• Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Experience with electronic data capture systems and software applications.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Strong problem-solving and analytical skills.
• Familiarity with ICH guidelines and other relevant regulations.

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