Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will play a vital role in our clinical trials, overseeing data collection, monitoring compliance, and ensuring accuracy in our datasets. Your expertise will contribute significantly to our research objectives.

Responsibilities

• Prepare and review case report forms (CRFs) and database specifications.
• Collaborate with research teams to ensure adherence to study protocols.
• Generate and distribute data reports as necessary for stakeholders.
• Oversee compliance with Good Clinical Practice (GCP) guidelines.
• Assist in the management of multiple clinical trials concurrently.
• Provide training to new team members on data management processes.
• Participate in regular meetings with clinical teams to discuss data findings.
• Identify areas for workflow improvements within data management.
• Ensure all activities comply with relevant ethical standards.
• Document all data management procedures accurately.

Advantageous

• Experience with Multiple Clinical Trials: Proven ability to manage data for multiple studies simultaneously.
• Familiarity with Regulatory Guidelines: Knowledge of ICH GCP, FDA, and EMA regulatory frameworks.

Benefits

• Annual salary reviews
• Employee assistance programme
• Generous holiday allowance and paid leave
• Team-building activities and social events

Company Culture

• Continuous Improvement: We strive for excellence through continuous learning and adaptation.
• Employee Development: Providing opportunities for professional growth is a priority for us.
• Social Responsibility: We are dedicated to making a positive impact on our community and the environment.