Clinical Research Assistant - 20 hrs per week

As a Clinical Research Assistant at CTTX Health, your primary responsibilities will encompass a variety of monitoring activities and ensuring compliance with study protocols. You will manage monitoring visits, including PSVs, SIVs, IMVs, and COVs, to guarantee that the research aligns with regulatory standards. Creating detailed monitoring reports that adhere to study timelines is crucial, as is the execution of source data verification (SDV) across multiple systems. You'll also oversee informed consent reviews, manage safety data, and perform home health visits, all contributing to the successful navigation of clinical trials.

To apply for the Clinical Research Assistant position at CTTX Health, candidates must possess at least one year of CRA experience specifically within the UK healthcare system. Additionally, a GCP certification is mandatory to demonstrate a thorough understanding of Good Clinical Practice standards. Familiarity with the UK regulatory landscape and a strong commitment to adhering to ethical standards in research will enhance your application, ensuring you align with CTTX's dedication to excellence in clinical trials.

CTTX Health goes the extra mile to support its Clinical Research Assistants with incredible benefits tailored to enhance your work-life balance and professional growth. As a part-time position, it offers flexibility with a 20-hour workweek, allowing you to manage personal commitments while contributing to meaningful research. Beyond competitive pay, CTTX emphasizes personal connections and mentorship, ensuring you feel valued and supported throughout your journey with us. We believe in investing in our team, providing resources for continued learning and advancement in your career.

CTTX Health is deeply committed to the career development of its Clinical Research Assistants. We offer training sessions and access to resources that prepare you for the various aspects of clinical research. Our focus on mentorship means you’ll receive guidance from experienced professionals, making it easier to navigate complexities in your role. Additionally, we encourage professional engagement within the healthcare community, providing opportunities for networking and continued education to help you grow and excel in your career.

Yes! At CTTX Health, we understand the importance of flexibility, especially in the healthcare sector. As a Clinical Research Assistant, you will have the opportunity to engage in both remote and on-site monitoring activities. We recognize that certain tasks may be effectively executed from a remote setting, allowing you to balance your professional responsibilities with personal commitments. This flexibility is a key aspect of our supportive environment, ensuring you thrive in your role while maintaining a healthy work-life balance.

In responding to this question, it’s effective to mention specific tasks and experiences related to source data verification (SDV). Highlight instances where you verified data for accuracy against source documents, what tools or systems you used, and how you ensured compliance with regulatory standards. Demonstrating your ability to identify discrepancies and how you handled them will showcase your attention to detail and commitment to quality in clinical research.

To answer this question, discuss your approach to familiarizing yourself with study protocols, including thorough reviews and continuous monitoring. Explain how you implement quality checks and follow-up on assigned tasks during the study phases to maintain compliance. Highlight your proactive communication with study teams to address any potential protocol deviations and your methods for documenting adherence through reports and meetings.

Discuss a specific challenge you've encountered in clinical trials, perhaps related to patient recruitment, data discrepancies, or regulatory compliance. Offer insights into the problem-solving methods you employed to address the issue, such as collaboration with stakeholders, adapting processes, or using technological solutions. This demonstrates your critical thinking capacity and adaptability under pressure.

Showcase your dedication to staying informed by mentioning specific resources you use to keep up with regulatory changes, such as relevant websites, professional networks, or continuing education courses. Discuss how you implement this knowledge in your work to enhance compliance and improve study procedures. This will reflect your commitment to maintaining professional standards as a Clinical Research Assistant.

Share your personal motivations for entering the field of clinical research, emphasizing your passion for healthcare, desire to contribute to medical advancements, or interest in patient welfare. Highlight any relevant experiences that catalyzed your decision and how working at CTTX Health aligns with your values and career goals. This provides insight into your professional journey and commitment to the field.

Think of a specific project where teamwork was crucial and outline your role within the group. Focus on how collaborative efforts led to achieving project goals, and illustrate your communication skills and how you fostered a positive team dynamic. Discuss any challenges the team faced and how you contributed to resolving them, showcasing your ability to work harmoniously in a clinical environment.

When responding to this question, outline the steps you would take, starting from the identification of the deviation to documentation and reporting. Emphasize the importance of transparency and following standard operating procedures. Discuss how effective communication with relevant team members and regulatory bodies is key to addressing the deviation while maintaining the integrity of the study.

Share specific tools and software platforms you’ve used in your previous roles, explaining how you utilized them for tasks such as data collection, monitoring, and reporting. Mention any certifications related to these tools if applicable. This showcases your technical skills and ability to adapt to different systems that may be used in clinical settings.

Discuss your methods for effective task prioritization, such as creating to-do lists, setting deadlines, and employing project management techniques. Explain how you assess the urgency and importance of various tasks and perhaps provide an example of a time when you successfully managed competing deadlines to maintain study momentum.

Emphasize the significance of trust, transparency, and regular communication when building relationships with study site staff. Discuss your approach to creating rapport, understanding their challenges, and supporting them in maintaining compliance and efficiency in their responsibilities. Highlighting how you value collaboration will position you as a candidate who thrives in team-oriented environments.