Clinical Trials Coordinator

Job Description

Join our dynamic team as a Clinical Trials Coordinator, where your role will involve managing clinical trial protocols, ensuring adherence to regulations, and facilitating communication between all stakeholders. This is an exciting opportunity to contribute to cutting-edge medical research.

Responsibilities

• Oversee recruitment and retention strategies for clinical trial participants.
• Monitor the implementation of trial protocols and provide guidance to study staff.
• Collect and manage clinical data to ensure accuracy and compliance.
• Prepare and submit trial progress reports to sponsors and regulatory authorities.
• Conduct quality assurance checks to ensure adherence to good clinical practices.
• Coordinate with data management teams to ensure data integrity.
• Support the preparation of presentations and materials for study results.
• Assist in financial management of trial budgets and negotiate with suppliers.
• Collaborate with research teams to deliver successful clinical outcomes.

Requirements

Education

• Master's degree in a relevant field is preferred
• Certification in GCP, ICH, or other relevant training is a plus

Experience

• 3+ years experience in clinical trials or project management

Technical Skills

• Clinical Research Regulations
• Project Management Tools

Soft Skills

• Problem-solving
• Attention to Detail

Languages

• English: Fluent

Advantageous

• Experience with patient recruitment strategies: Ability to devise creative strategies for participant engagement.
• Experience in healthcare project management: Knowledge of managing healthcare-related projects effectively.