Freelance Clinical Research Associate - job 1 of 2

As a Freelance Clinical Research Associate at ClinChoice, your responsibilities will include monitoring clinical trial sites, performing trainings, ensuring compliance with protocols and regulatory guidelines, and managing data integrity throughout the studies. You will also engage in site selection and evaluation, address any safety issues, and provide general support to the Clinical Research Division, ensuring successful project completion.

To qualify as a Freelance Clinical Research Associate with ClinChoice, candidates must possess a university degree in a scientific medical or paramedical discipline and have prior experience as a CRA with demonstrated on-site monitoring activities. A strong knowledge of GCP/ICH Guidelines, proficiency in English and Dutch, and Microsoft Office skills are essential for this role.

Yes, travel is an essential part of the Freelance Clinical Research Associate position at ClinChoice. You will be required to conduct site monitoring visits and ensure that trials are effectively managed across various locations, which means regular travel will be involved.

At ClinChoice, we believe that our employees are our greatest asset. As a Freelance Clinical Research Associate, you’ll benefit from continuous training and development programs designed to enhance your clinical trial management skills and keep you updated on the latest industry standards and regulatory requirements.

The application process for the Freelance Clinical Research Associate position at ClinChoice begins with submitting your CV. If your background aligns with our requirements, you will be invited for a phone interview as the first step. We appreciate your interest in joining our team and wish you the best in your application!

When answering this question, highlight specific monitoring visits you've conducted, how you ensured data integrity, and your understanding of compliance with GCP and protocol requirements. Discuss any challenges faced and how you resolved them, showcasing your attention to detail and commitment to safety.

Demonstrate your familiarity with ICH-GCP guidelines by explaining the steps you take to train site staff, monitor compliance during site visits, and conduct regular checks on documentation. Sharing any real-life examples of how you've implemented these measures will also strengthen your response.

Discuss the importance of communication, trust-building, and transparency in managing relationships with site staff. Provide examples of how you establish these relationships and maintain them through regular check-ins and support, ensuring that issues are addressed promptly.

Explain your process for identifying, documenting, and escalating safety issues. Emphasize your commitment to participant safety and compliance with regulatory requirements, and provide examples of how you’ve effectively handled any reported adverse events in past roles.

Highlight your proficiency with specific software tools used for clinical data management, such as EDC systems or CRF management tools. Discuss any experiences tracking and resolving data queries using these tools and how they contribute to efficient trial management.

Share a specific incident where a study faced challenges, detailing your approach to assessing the situation, the actions you took to mitigate the issues, and the outcome. Focus on your problem-solving skills and ability to adapt to ensure project objectives are met.

Discuss the various methods you use to stay informed about changes in regulations, clinical trial practices, and GCP guidelines. This can include attending conferences, participating in workshops, and following industry publications—showing your dedication to continuous learning.

Emphasize the importance of clear communication when training site staff. Discuss how you develop training materials, engage staff during training sessions, and ensure they understand the protocol, ICH-GCP principles, and documentation processes for successful trial execution.

Describe your organizational skills and the tools or techniques you use to prioritize tasks effectively. Mention any project management strategies or software that help you manage timelines and stay focused on critical tasks across multiple studies.

When discussing your motivation, highlight ClinChoice's commitment to quality and professional development. Share your passion for contributing to innovative drug development and how the supportive culture aligns with your career goals and values.