Clinical Trial Assistant, (UK) Remote
Clinical Trial Assistant, (UK) Remote

Clinical Trial Assistant, (UK) Remote

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support clinical trials with essential admin and operational tasks in a dynamic remote environment.
  • Company: Join CellCentric, a forward-thinking company focused on teamwork and innovation.
  • Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
  • Why this job: Make a real impact in healthcare while developing your skills in a supportive team.
  • Qualifications: Degree in life sciences preferred; relevant experience considered.
  • Other info: Embrace a culture of trust, respect, and collaboration.

The predicted salary is between 36000 - 60000 £ per year.

The Clinical Trial Assistant (CTA) provides essential administrative and operational support to the Clinical Operations team for late-stage clinical trials. This individual will contribute to the success of the team and organization by delivering role-specific responsibilities while upholding our core working behaviours of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement.

Key Responsibilities

  • Maintain Trial Master File (TMF) filing in compliance with applicable GCP requirements and CellCentric SOPs.
  • Creation and compilation of investigator site files.
  • Ensure all documentation is filed and maintained according to GCP and company SOPs.
  • Track and manage study approvals, protocol amendments, and essential documentation updates.
  • Assist in setting up investigator meetings, site initiation visits, and study monitoring visits.
  • Maintain communication with clinical trial sites, ensuring timely collection of documents and adherence to study timelines.
  • Track site activation, recruitment progress, and key trial milestones.
  • Support data entry, query resolution, and reconciliation of trial-related information.
  • Prepare study reports, meeting minutes, and status updates for internal and external stakeholders.
  • Support the tracking of clinical trial budgets and invoices related to investigator payments and vendor services.
  • Assist in developing and maintaining SOPs relevant to clinical trial operations.
  • Provide administrative support for clinical team meetings, including scheduling, agenda preparation, and minute-taking.
  • Manage trial-related correspondence and maintain organized records.
  • Support the Clinical Operations Team with appropriate project and site management activities, as required.
  • Travel with the CRAs on site to help and assist with the investigator site file and ad hoc site tasks.
  • Adhering to Company Standard Operating Procedures, Policies and applicable regulatory requirements.
  • Execute day-to-day responsibilities of the role, ensuring quality, accuracy, and timeliness.
  • Collaborate effectively with colleagues, sharing knowledge and supporting team goals.
  • Contribute to problem-solving and decision-making processes with an objective, data-driven approach.
  • Communicate clearly and proactively with stakeholders to ensure alignment.
  • Demonstrate ownership of tasks and follow through to successful completion.
  • Support team members through constructive feedback, mentorship, and collaboration.

Skills and Qualifications

  • A degree in a life science or health-related discipline is preferred. Candidates with relevant clinical research, healthcare, or administrative experience may be considered in lieu of a degree.
  • Previous experience as a CTA on a CRO/Pharma or Biotech.
  • Strong interpersonal and communication skills, with the ability to adapt to different audiences.
  • Proven ability to build trust and credibility through integrity, openness, and respect.
  • Demonstrated accountability in delivering results and meeting commitments.
  • Analytical mindset with the ability to use facts and data to guide decisions.
  • Ability to work both independently and collaboratively within a team.

Working Behaviours (Core Expectations)

  • Trust and Respect: Act with integrity, honesty, and openness to build strong, credible relationships.
  • Communication and Feedback: Share information clearly, listen actively, and engage in a culture of constructive feedback.
  • Accountability and Reliability: Take ownership for performance, be dependable, and support others to achieve collective goals.
  • Objectivity: Align on common objectives and use facts and data to reach fair, effective decisions.
  • Team Balance and Enablement: Contribute to balanced roles within the team, support delegation, and help colleagues reach their full potential.

Why Join Us?

At CellCentric we believe success is built on great teams. By embodying these working behaviours, every member contributes to a high-performing, supportive, and inclusive culture where individuals and the business thrive together.

Clinical Trial Assistant, (UK) Remote employer: CellCentric Limited

CellCentric is an exceptional employer that fosters a collaborative and inclusive work environment, particularly for the Clinical Trial Assistant role. With a strong emphasis on trust, respect, and accountability, employees are encouraged to grow through mentorship and constructive feedback while contributing to meaningful clinical research. The remote nature of this position allows for flexibility, enabling team members to balance their professional and personal lives effectively.
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Contact Detail:

CellCentric Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trial Assistant, (UK) Remote

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend virtual events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.

✨Tip Number 2

Prepare for interviews by researching the company and understanding their values. Be ready to discuss how your skills align with their core working behaviours like Trust and Respect, and Accountability. Show them you’re not just a fit for the role, but for the team culture too!

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or use online platforms to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s time to shine in front of the real interviewers.

✨Tip Number 4

Don’t forget to follow up after interviews! A simple thank-you email can go a long way in showing your appreciation and keeping you top of mind. Plus, it’s a great chance to reiterate your enthusiasm for the role and the company.

We think you need these skills to ace Clinical Trial Assistant, (UK) Remote

GCP Compliance
Trial Master File Management
Document Management
Study Approval Tracking
Meeting Coordination
Communication with Clinical Trial Sites
Data Entry and Query Resolution
Budget Tracking
SOP Development
Minute-Taking
Interpersonal Skills
Analytical Mindset
Team Collaboration
Problem-Solving
Time Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Assistant role. Highlight any relevant experience in clinical research or administrative support, and don’t forget to showcase your strong communication skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your values align with our core behaviours like Trust and Respect. Keep it concise but impactful!

Showcase Your Skills: In your application, be sure to highlight your organisational skills and attention to detail. Mention any experience with maintaining documentation or managing timelines, as these are key for the CTA role.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!

How to prepare for a job interview at CellCentric Limited

✨Know Your GCP and SOPs

Familiarise yourself with Good Clinical Practice (GCP) guidelines and the specific Standard Operating Procedures (SOPs) of the company. This knowledge will not only help you answer questions confidently but also demonstrate your commitment to compliance and quality in clinical trials.

✨Showcase Your Communication Skills

Since the role involves maintaining communication with clinical trial sites, be prepared to discuss how you've effectively communicated in past roles. Use examples that highlight your ability to adapt your communication style to different audiences, ensuring clarity and engagement.

✨Demonstrate Team Spirit

Emphasise your experience working collaboratively within a team. Share specific instances where you supported colleagues or contributed to team goals, showcasing your understanding of the importance of trust, respect, and accountability in a high-performing environment.

✨Prepare for Problem-Solving Questions

Expect questions that assess your analytical mindset and decision-making skills. Prepare examples where you used data to guide your decisions or resolved conflicts within a team. This will illustrate your objectivity and ability to contribute to effective problem-solving processes.

Clinical Trial Assistant, (UK) Remote
CellCentric Limited
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