Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust
Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust

Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust

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

  • Tasks: Coordinate clinical trials, manage documentation, and liaise with research teams.
  • Company: Join The Christie NHS Foundation Trust, Europe's largest cancer treatment centre and a leader in cancer research.
  • Benefits: Enjoy a supportive work environment, professional development opportunities, and the chance to make a real impact.
  • Why this job: Be part of groundbreaking cancer research and help improve patient outcomes in a dynamic team.
  • Qualifications: Experience in clinical trials administration and strong organisational skills are essential.
  • Other info: This role offers a unique opportunity to contribute to innovative cancer treatments.

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

This is an exciting opportunity to join the Experimental Cancer Medicine Team (ECMT) at The Christie NHS Foundation Trust; an international leader in cancer research and development and the largest cancer treatment centre of its kind in Europe.

The post holder will have experience in clinical trials administration, particularly in trials set up, and will work alongside the clinical team on a portfolio of early phase trials.

We are seeking an enthusiastic, motivated and experienced individual who will be responsible for various aspects of clinical trial coordination including liaising with trial sponsors, monitors and the wider research community, maintaining essential documentation, managing the set-up of new studies and overseeing the day to day running of open studies.

The successful candidate will need to demonstrate knowledge of the clinical trials process, and be IT literate with previous experience of administrative work. We are looking for a candidate with good organisation and communication skills; who can work well both in a team and using their own initiative.

Senior Clinical Trials Coordinator – For Main duties of the job – See Detailed Job Description and Person Specification – Attached

The Christie is one of Europe’s leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country.

We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years.

We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.

DUTIES AND RESPONSIBILITIES

Team Support

· Responsible for supporting and supervising workload allocation/ monitoring across administrative team members, escalating issues as appropriate to senior managers.

· Provide support to senior managers with general Human Resource activities, including but not limited to recruitment and selection and line management of administrative team members as required. This will be in accordance with Trust policies.

· Provide induction support and training to new and existing clinical trials staff through one-to-one and group learning activities.

· Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff.

· Assist with data collection for divisional metrics reports of key performance indicators.

CLINICAL TRIALS CO-ORDINATION/ DATA MANAGEMENT:

The specific responsibilities will depend on the requirements of each team, but may include:

· Act as a key point of contact with the core Research and Development team, study sponsors, clinical research organisations and specific research teams.

· Support feasibility activities for new studies under direction from senior managers and Principal Investigators.

· Manage the set up and initiation of allocated clinical trials within assigned Clinical Research Teams. Provide support for study set up and initiation that has been delegated to Clinical Trials Coordinators, escalating any delays as appropriate.

· Support with negotiations of study set-up costs and income recovery for assigned clinical trials in conjunction with the Research Division’s Business Planning and Finance teams with oversight from senior managers.

· Oversee maintenance of investigator site files and essential documentation in accordance with ICH-GCP and Trust Standard Operating Procedures (SOPs) to ensure they are kept inspection ready at all times.

· Oversee and process trial amendment submissions in accordance with ICH-GCP and Trust SOPs and timelines, escalating any delays with the core Research and Development office as appropriate.

· To have the appropriate administrative processes in place to ensure, with the Clinical Research Team, that adverse event incidents and forms are completed, reported and followed up to resolution as the study protocol and regulations require.

· Implement and coordinate reporting mechanisms to ensure that research staff complete and return proformas containing up-dated information on patients included in the study.

· Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements.

· Liaise with internal staff and external collaborators to resolve queries.

· Provide information for senior managers including (but not limited to) case report form completion timeliness, data locks, data backlogs, work allocations and patient recruitment.

· Ensure that data is available and up to date for any meetings related to the trial/ study, producing minutes as required.

· Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.

· Attend disease-specific research team meetings to maintain an overview of team activity.

· Assist with preparation for audit and inspections within assigned teams and implementation of action plans.

· Ensure that all documents are archived in the appropriate way by following the Trust’s archiving guidelines.

· Undertake general administrative tasks as delegated by managerial representatives from the Research Division to contribute to the smooth running of the patient recruitment teams.

· Demonstrates the agreed set of values and accountable for own attitude and behaviour

WORKING PRACTICE

· Work closely with the Senior Research Management Team to implement new SOPs and working procedures within designated teams.

· Be pro-active in providing feedback on working practices within the research team and suggest new ways of working.

· The post holder is expected to use initiative and be able to work independently without close supervision. They are also expected to plan and organise their own time and workload activity with prioritisation, referring to senior managers as necessary.

· The post holder is guided by relevant protocols and SOPs, and expected to exercise judgement outside these areas.

PERSONAL AND PEOPLE DEVELOPMENT

· Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework.

· Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.

PHYSICAL, MENTAL AND EMOTIONAL EFFORT

· Long periods of time spent using keyboard to input information and use of VDU for electronic communication.

· Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets).

· Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.

This advert closes on Wednesday 30 Jul 2025 #J-18808-Ljbffr

Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust employer: The Christie NHS Foundation Trust

The Christie NHS Foundation Trust is an exceptional employer, renowned for its commitment to cancer research and patient care. Located in Manchester, it offers a collaborative work culture that fosters professional growth through continuous training and development opportunities, while also providing the chance to be part of groundbreaking clinical trials that make a real difference in patients' lives. Employees benefit from working in one of Europe's largest cancer treatment centres, with access to state-of-the-art facilities and a supportive team environment that values innovation and excellence.
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Contact Detail:

The Christie NHS Foundation Trust Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust

✨Tip Number 1

Familiarise yourself with the latest trends and regulations in clinical trials. Understanding ICH-GCP guidelines and the specific protocols used at The Christie NHS Foundation Trust will give you an edge during interviews.

✨Tip Number 2

Network with professionals in the field of clinical trials, especially those who have experience at The Christie or similar institutions. Attend relevant conferences or seminars to make connections that could lead to valuable insights or referrals.

✨Tip Number 3

Prepare to discuss your previous experiences in clinical trials coordination in detail. Be ready to share specific examples of how you've managed trial set-ups, liaised with sponsors, or handled documentation to demonstrate your expertise.

✨Tip Number 4

Showcase your organisational and communication skills during any interactions with the team. Being proactive and demonstrating your ability to work independently while also being a team player will resonate well with the hiring managers.

We think you need these skills to ace Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust

Clinical Trials Administration
Knowledge of ICH-GCP Guidelines
Data Management Skills
Strong Communication Skills
Organisational Skills
Team Leadership and Supervision
Problem-Solving Skills
Attention to Detail
Ability to Work Independently
Experience with Trial Set-Up and Coordination
Familiarity with Regulatory Compliance
Proficiency in Microsoft Office Suite
Time Management Skills
Training and Induction Skills
Ability to Handle Sensitive Information

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials administration. Focus on your previous roles, particularly those involving trial set-up and coordination, and emphasise your organisational and communication skills.

Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities outlined in the job description. Mention your enthusiasm for cancer research and how your background aligns with the needs of The Christie NHS Foundation Trust.

Highlight Relevant Skills: In your application, clearly demonstrate your knowledge of the clinical trials process and IT literacy. Provide examples of how you've successfully managed documentation and liaised with various stakeholders in past roles.

Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for the role of Senior Clinical Trials Coordinator.

How to prepare for a job interview at The Christie NHS Foundation Trust

✨Know Your Clinical Trials Inside Out

Make sure you have a solid understanding of the clinical trials process, especially early phase trials. Be prepared to discuss your previous experiences in trial administration and how they relate to the role at The Christie NHS Foundation Trust.

✨Showcase Your Organisational Skills

As a Senior Clinical Trials Coordinator, you'll need to manage multiple tasks simultaneously. Prepare examples of how you've successfully organised and prioritised workloads in past roles, demonstrating your ability to keep everything running smoothly.

✨Communicate Effectively

Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely, and be ready to explain how you've liaised with various stakeholders in previous positions, such as sponsors and research teams.

✨Demonstrate Initiative and Problem-Solving

The role requires someone who can work independently and proactively address challenges. Think of instances where you've identified issues and implemented solutions without waiting for direction, and be ready to share these examples during your interview.

Senior Clinical Trials Coordinator | The Christie NHS Foundation Trust
The Christie NHS Foundation Trust
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