Clinical Research Coordinator

Job Description

We are looking for a Clinical Research Coordinator to oversee clinical trials and research projects. The ideal candidate will manage recruitment, data collection, and compliance with regulatory standards, ensuring the successful execution of studies.

Responsibilities

• Lead initial feasibility assessments for new trials and studies.
• Ensure informed consent processes are clearly communicated and documented.
• Assist in the preparation of research grant proposals.
• Identify and mitigate risks associated with trial execution.
• Conduct periodic audits to ensure compliance with protocols.
• Foster a supportive and inclusive environment for research participants.
• Manage budgets and resources effectively to meet study needs.

Requirements

Education

• Ph.D. in clinical research or related discipline
• Relevant certifications or additional training preferred

Experience

• 5+ years of experience managing clinical trials

Technical Skills

• Research Methodology
• Statistical Software

Soft Skills

• Leadership
• Negotiation

Certifications

• Certified Clinical Research Coordinator (CCRC)
• Good Clinical Practice (GCP)

Languages

• English: Fluent

Advantageous

• Familiarity with electronic data capture (EDC) systems: Experience with tools like Medidata and REDCap.
• Understanding of regulatory requirements: Deep knowledge of MHRAs and FDA regulations.

Benefits

• Flexible work arrangements
• Generous annual leave entitlement
• Wellness programmes and support
• Access to research and training resources

Company Culture

• Professional Growth: We offer numerous opportunities for professional growth, including training and mentorship programmes.
• Supportive Work Environment: Our team is supportive and values a healthy work-life balance.
• Open Communication: We practice open communication and transparency in our organization.