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Clinical Research Assistant - 20 hrs per week

CTTX Health is a boutique healthcare recruiting agency. We place individuals in both permanent and temporary contracts. How are we different from all the other companies? We care! We pick up the phone and talk about you.

CTTX is a small, women-owned company. We don't want you to be a number or have recruiters pushing you into the wrong positions. Honestly, we all have the same opportunities, the difference is how we care for you. CTTX values your work and wants to relieve the stress of finding your dream job.

Here is what you really want to know;

  • Monitoring visits including but not limited to PSVs (Pre-Study Visits), SIVs (Site Initiation Visits), IMVs (Interim Monitoring Visits), and COV (Close Out Visits) 
  • Adherence to Study Monitoring Plan 
  • Delivery of Monitoring Reports that align with study timelines 
  • Central Monitoring review 
  • Perform SDV (Source Data Verification) and Monitoring activity for study (remote and On-site) 
  • SDV across multiple systems and multiple vendors 
  • SDV of all Screening and Enrollment Data across participants  
    • Informed Consent Review/SDV 
    • Safety data (vitals, ECGs, lab results) g. Protocol Deviations 
    • Dispensation and Study Drug Administration and Accountability 
    • Home Health/Telehealth Visits 
    • Clinical Laboratory Evaluations and ECGs 
  • Site Management – virtual and on-site  
  • Study Training/Protocol Training  
  • Must have at least 1 year of CRA experience in the UK 
  • Must be GCP certified 
  • Familiarization with UK Regulatory requirements 

Amazing benefits

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What You Should Know About Clinical Research Assistant - 20 hrs per week, CTTX Health

Join CTTX Health as a Clinical Research Assistant for 20 hours per week and immerse yourself in an empowering role that focuses on the heart of healthcare research. At CTTX, a boutique healthcare recruiting agency with a personal touch, we pride ourselves on placing you in roles that truly fit your skills and passions. We’re not just another recruitment agency – we’re a small, women-owned company that genuinely cares about you and your career journey. As a Clinical Research Assistant, your responsibilities will include essential tasks like monitoring visits, conducting exploratory site visits, and ensuring adherence to study monitoring plans. You'll deliver comprehensive monitoring reports that align with rigorous study timelines and execute source data verification across various platforms. Whether it's performing informed consent reviews or participating in home health and telehealth evaluations, your role will be pivotal in shaping the future of patient care. With at least one year of CRA experience in the UK and a GCP certification, you'll navigate regulatory requirements while contributing to clinical excellence. If you're ready to be part of a supportive team that values your contributions and strives to minimize the stress of job hunting, CTTX Health is the place for you. Experience amazing benefits and a nurturing work environment that recognizes and rewards your efforts. Let's redefine healthcare recruitment together!

Frequently Asked Questions (FAQs) for Clinical Research Assistant - 20 hrs per week Role at CTTX Health
What responsibilities does a Clinical Research Assistant at CTTX Health have?

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.

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What qualifications do I need to apply for the Clinical Research Assistant position at CTTX Health?

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.

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What unique benefits does CTTX Health offer to Clinical Research Assistants?

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.

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How does CTTX Health support the career development of Clinical Research Assistants?

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.

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Is remote work an option for Clinical Research Assistants at CTTX Health?

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.

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Common Interview Questions for Clinical Research Assistant - 20 hrs per week
Can you describe your experience with source data verification as a Clinical Research Assistant?

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.

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How do you ensure adherence to study protocols?

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.

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What challenges have you faced in clinical trials, and how did you overcome them?

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.

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How do you keep up with changes in UK regulations regarding clinical trials?

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.

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Why did you choose to work 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.

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Describe a time you worked effectively as part of a team.

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.

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How would you handle a protocol deviation?

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.

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What tools or software are you familiar with for clinical trial management?

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.

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How do you prioritize your tasks during a busy study period?

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.

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What do you consider most important for building relationships with study site staff?

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.

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EMPLOYMENT TYPE
Part-time, remote
DATE POSTED
March 2, 2025

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