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- Tasks: Support clinical studies from start-up to close-out, ensuring compliance and efficiency.
- Company: Join TFS HealthScience, a leading global Contract Research Organization.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for personal and professional growth.
- Why this job: Make a real difference in patients' lives while working with a dedicated team.
- Qualifications: Bachelor's degree preferred with 3+ years of relevant experience as a CTA.
- Other info: Hybrid role with a collaborative culture focused on innovation and excellence.
The predicted salary is between 36000 - 60000 £ per year.
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service (FSP) solutions.
As a Clinical Trial Associate you will play a key role in supporting clinical studies from start-up to close-out. You will ensure compliance, accuracy and efficiency in study documentation and coordination. Working closely with the Project Manager, Lead CRA and Study Team you will help drive operational excellence across all phases of the clinical trial. As part of our SRS/FSP team you will be dedicated to one sponsor, a Big Pharma company. Please keep in mind that this is a hybrid role with 3 days per week working from an office in Luton.
Key Responsibilities- Organize, maintain and archive the Study Master File (SMF) in accordance with GCP SOPs and regulatory requirements.
- Support study setup and maintenance in the Clinical Trial Management System (CTMS).
- Prepare and manage Investigators Files and coordinate study supplies.
- Prepare and distribute trial-related documents, tools and templates.
- Arrange and document internal and external meetings including taking meeting minutes.
- Assist with audits and regulatory inspections.
- Assist with site contracts, investigator payments and translation processes.
- Act as Lead CTA or mentor to junior team members when assigned.
- Bachelor's degree preferred.
- 3-5 years of relevant experience including at least 3 years as a CTA.
- Strong knowledge of GCP/ICH guidelines.
- Excellent written and verbal communication skills.
- Highly organized with strong attention to detail and the ability to manage multiple priorities.
- Proficient in Microsoft Office and relevant clinical systems.
We provide a competitive compensation package, comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation and making a difference in the lives of patients.
A Bit More About UsOur journey began over 27 years ago in Sweden in the city of Lund. As a full-service global Contract Research Organization (CRO) we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.
Our core values of Trust, Quality, Passion, Flexibility and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
Senior Clinical Trial Associate employer: TFS HealthScience
Contact Detail:
TFS HealthScience Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Trial Associate
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with yours. We want you to show up not just as a candidate, but as someone who genuinely fits into their team and mission.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We believe that being well-prepared can make all the difference when it comes to impressing your interviewers.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in leaving a positive impression. We recommend reiterating your interest in the role and mentioning something specific from your conversation to keep you fresh in their minds.
We think you need these skills to ace Senior Clinical Trial Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Trial Associate role. Highlight your relevant experience, especially in clinical trials and GCP/ICH guidelines. We want to see how your skills align with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your background makes you a perfect fit. Don’t forget to mention your organisational skills and attention to detail, as these are key for us.
Showcase Your Communication Skills: Since excellent written and verbal communication is crucial for this position, make sure your application reflects that. Keep your language clear and professional, and don’t hesitate to demonstrate your ability to manage multiple priorities.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at TFS HealthScience!
How to prepare for a job interview at TFS HealthScience
✨Know Your GCPs
Make sure you brush up on Good Clinical Practice (GCP) and ICH guidelines before your interview. Being able to discuss these in detail will show that you’re not just familiar with the basics, but that you truly understand their importance in clinical trials.
✨Showcase Your Organisational Skills
As a Senior Clinical Trial Associate, organisation is key. Prepare examples of how you've successfully managed multiple priorities in past roles. This could be through managing study documentation or coordinating meetings—anything that highlights your attention to detail and ability to juggle tasks.
✨Familiarise Yourself with CTMS
Since you'll be supporting study setup in the Clinical Trial Management System, it’s crucial to know your way around it. If you have experience with specific systems, be ready to discuss how you’ve used them effectively in previous roles.
✨Prepare for Team Dynamics
You’ll be working closely with Project Managers and CRAs, so think about how you can demonstrate your teamwork skills. Be prepared to share instances where you’ve acted as a mentor or led a project, showcasing your leadership abilities and collaborative spirit.
