Clinical Trial Expert

Clinical Trial Expert

Temporary 60000 - 75000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical trials, ensuring quality and collaboration with stakeholders.
  • Company: Join a top biopharmaceutical company improving lives with innovative medicines.
  • Benefits: Enjoy a competitive salary, flexible remote work, and a dynamic team environment.
  • Why this job: Be part of impactful research in a fast-paced, collaborative setting.
  • Qualifications: Degree in life sciences or equivalent experience; drug development knowledge required.
  • Other info: Must be eligible to work in the UK and may require a DBS check.

The predicted salary is between 60000 - 75000 £ per year.

CK Group are recruiting for a Clinical Trial Expert to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 12 months.

Salary: Daily £400.00 - £450.00 Umbrella / £301.57 - £339.27 PAYE (this role is inside IR35).

Role: With a strong background in trial execution contribute to specific study strategies. Establishes and maintains optimal relationships with key internal partners, stakeholder groups, and external partners. Clinical Trial Experts support the quality of CTs by participating in audits and inspection readiness through the study lifecycle while contributing to CAPAs as required. Leadership role in the implementation of systems maintenance, tools and reports required across the clinical trial life cycle (eCOA, IxRS etc). Coordinating imaging and rater components of study startup, including input into requests for proposal, authoring of documents and potentially site personnel training. Contribute to the development and maintenance of relevant study oversight documentations/charters (i.e. trial risk management plan, communication plan, monitoring plan, data cleaning plan, etc.). Track clinical study progress and address issues that may come up in close collaboration with study teams, affiliates, sites, and CROs as appropriate. Collaborate with stakeholders in generating relevant reports and KPIs to monitor trial progress.

Your Background: Have a growth mindset and are excited about learning through experience. Feel comfortable thinking on your feet and thrive in fast paced, ambiguous and highly collaborative environments. Have experience in pharmaceutical and/or healthcare industry and drug development experience (therapeutic area experience a plus). Hold a university degree or equivalent years of experience, preferred focus in life sciences. Possess strong working knowledge of drug development process and respective regulations. Feel comfortable traveling internationally based on specific program needs. Experience of healthy volunteer studies, and doing study close outs is a must.

Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Location: This role is based at our client's site in Welwyn Garden City, for 2-3 days per week, and remote for the remainder of the week.

Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 123 837 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Clinical Trial Expert employer: CK Group

CK Group is an exceptional employer, offering a dynamic work environment in the heart of Welwyn Garden City, where innovation meets collaboration. With a strong focus on employee growth and development, our company provides opportunities to engage in meaningful projects that directly impact global health. Enjoy a competitive salary, flexible working arrangements, and the chance to be part of a leading biopharmaceutical company dedicated to improving lives worldwide.
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Contact Detail:

CK Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trial Expert

✨Tip Number 1

Network with professionals in the pharmaceutical industry, especially those who have experience in clinical trials. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in clinical trial execution.

✨Tip Number 2

Familiarise yourself with the specific tools and systems mentioned in the job description, such as eCOA and IxRS. Having hands-on experience or knowledge of these systems can set you apart from other candidates.

✨Tip Number 3

Demonstrate your leadership skills by discussing past experiences where you successfully coordinated teams or projects. Highlight your ability to maintain relationships with stakeholders and how you’ve contributed to study oversight documentation.

✨Tip Number 4

Stay updated on regulations and best practices in drug development. Showing that you are proactive about your professional development can impress hiring managers and demonstrate your commitment to the role.

We think you need these skills to ace Clinical Trial Expert

Clinical Trial Management
Regulatory Knowledge
Stakeholder Engagement
Audit and Inspection Readiness
Risk Management
Data Analysis
Project Coordination
Communication Skills
Problem-Solving Skills
Knowledge of eCOA and IxRS Systems
Experience with Healthy Volunteer Studies
Training and Development
Collaboration Skills
Adaptability in Fast-Paced Environments

Some tips for your application 🫡

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Clinical Trial Expert position. Tailor your application to highlight relevant experiences that align with these expectations.

Highlight Relevant Experience: Emphasise your background in the pharmaceutical or healthcare industry, particularly any experience with clinical trials, drug development, and study close-outs. Use specific examples to demonstrate your expertise.

Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the role and the company. Mention your growth mindset and ability to thrive in fast-paced environments, as these traits are valued by the employer.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the clinical trial field.

How to prepare for a job interview at CK Group

✨Showcase Your Experience

Be prepared to discuss your previous experience in clinical trials, particularly any roles that involved trial execution and stakeholder management. Highlight specific examples where you contributed to study strategies or maintained relationships with key partners.

✨Demonstrate Your Knowledge

Familiarise yourself with the drug development process and relevant regulations. During the interview, confidently discuss how your knowledge aligns with the requirements of the role, especially regarding audits, inspections, and CAPAs.

✨Emphasise Your Growth Mindset

The company values a growth mindset, so be ready to share instances where you've learned from challenges or adapted to fast-paced environments. This will show your potential to thrive in their collaborative setting.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your problem-solving skills and ability to think on your feet. Practice articulating how you would handle specific challenges related to clinical trial progress and stakeholder collaboration.

Clinical Trial Expert
CK Group
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  • Clinical Trial Expert

    Temporary
    60000 - 75000 £ / year (est.)

    Application deadline: 2027-03-23

  • C

    CK Group

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