Clinical Trial Administrator

Royal Marsden

Carshalton

On-site

GBP 26,000 - 32,000

Full time

4 hours ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

The Royal Marsden NHS Foundation Trust in Sutton is seeking a Clinical Trial Administrator to join the Breast Research team. The role involves essential administrative and data management support across our clinical trial portfolio, including data entry, query resolution, source documentation, monitoring visits, and trial archiving.

You will be highly organized with excellent attention to detail and strong IT skills, especially Excel.

Qualifications

  • Educated to at least GCSE/A level.
  • Knowledge of Good Clinical Practice (GCP).
  • Previous experience working in a clinical trials unit.
  • Understanding of medical terminology.

Responsibilities

  • Provide timely data entry and query resolution into the trial database (eCRF).
  • Support trial governance and unit administration to ensure efficient trial delivery.
  • Liaise with sponsor organisations and R&D departments as required.
  • Ensure timely completion of source documentation and trial archiving.

Skills

Microsoft Excel
Data entry
Attention to detail
Communication skills

Education

GCSE / A level

Tools

eCRF systems
Microsoft Office

Job description

An exciting opportunity has arisen to join the Breast Research team at The Royal Marsden as a Clinical Trial Administrator, based at our Sutton site.

The Royal Marsden is internationally recognised for cancer research and is at the forefront of developing and delivering innovative treatments. This role is an excellent opportunity to begin or develop a career in clinical research within a busy, supportive and experienced team.

You will provide essential administrative and data management support across our clinical trial portfolio, including entering trial data, resolving queries, maintaining study records, preparing source documentation, supporting monitoring visits and audits, processing patient expenses and assisting with trial archiving.

We are looking for a highly organised, motivated individual with excellent attention to detail, strong communication skills, and the ability to manage competing priorities. Strong IT skills, particularly Microsoft Excel, are essential. Previous administrative, database, or clinical trial experience and knowledge of Good Clinical Practice would be advantageous.

Occasional cross‑site working may be required. If you are proactive, dependable, and enthusiastic about contributing to high‑quality cancer research, we would love to hear from you.

Main duties of the job
  • To provide timely and accurate data entry and query resolution into the appropriate trial database (eCRF).
  • To support the Breast Research Governance team with study administration in order to ensure the efficient and successful delivery of clinical trials and other studies according to Good Clinical Practice (GCP), standard operating procedures (SOPs), trust policies, and all applicable regulations
    and governance.
Working for our organisation

The Royal Marsden NHS Foundation Trust is a world‑leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital.

At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.

At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on‑going achievements.

Detailed job description and main responsibilities

For further information please refer to the job description and personal specification

Primary areas of responsibility
  • To ensure trial data is entered into the appropriate databases and systems, and to ensure all queries are resolved in a timely manner.
  • To support the Clinical Research Operations Manager (CROM) with unit administration.
Communication & Networking
  • Liaise with external agencies (e.g. Sponsor organisations & R&D Departments) on behalf of CROM, Trials Coordinators or Research Nurses where required.
  • Act as a point of contact for trial sponsors and communicate with them directly regarding data queries, monitoring visits and other enquiries relevant to the trial and research team.
Decision Making, Planning and Problem Solving
  • Follow all relevant protocols, SOPs and standard practice.
  • Plan and organise own time and workload activity with prioritisation.
Service Delivery
  • Support and maintain unit operating systems & records - for example, patient recruitment logs.
  • Ensure that office & clinic supplies are adequate, ordered and obtained for the smooth running of the trials.
General responsibilities
  • To communicate effectively with other members of the team and centre.
  • To work in a flexible manner and be organised, meeting objectives and deadlines with the occasional need to work across either site where additional support may be required.
Education/Qualifications
  • Educated to at least GCSE/A level
  • Knowledge of Good Clinical Practice (GCP)
  • Previous experience working in a clinical trials unit
  • Understanding of medical terminology
Experience
  • Excellent knowledge of Microsoft Office applications, in particular Microsoft Excel
  • Experience working with databases
  • Experience of working in an administrative role
  • Experience of working in a busy environment
Skills/Abilities/Knowledge
  • Ability to prioritise own workload
  • Be trusted to work unsupervised when appropriate
  • Ability to maintain excellent interpersonal & communication skills with a wide range of people (e.g., medical & nursing staff, managers and pharmaceutical industry representatives)
  • Ability to grasp new concepts quickly
Personal Qualities
  • Ability to remain calm whilst under pressure
  • Flexibility to meet the needs of the role

The Royal Marsden values diversity and is committed to the recruitment and retention of underrepresented minority groups. We particularly welcome applications from Black, Asian and minority ethnic candidates, LGBTQ+ candidates and candidates with disabilities.

As a Disability Confident Employer, we are working to create a workplace that enables all staff to reach their full potential. We are committed to this because we know that greater diversity and inclusion will lead to an even greater positive impact for the people we serve.

Due to the high volumes of applications we receive, we reserve the right to close any adverts before the published closing date once we have received a sufficient number of applications. We advise you to submit your application as early as possible to prevent disappointment. Please ensure your information is accurate to avoid errors with processing your application

All applicants will be contacted by email to the address supplied on your application. Applicants are advised to check their email accounts regularly and to ensure that email filters are set to allow our emails.

Flu Vaccination - What We Expect of our Staff

At The Royal Marsden we have an immune compromised patient population who we must protect as much as we can against the flu virus. Each year, seasonal flu affects thousands of people in the UK. Occurring mainly in winter, it is an infectious respiratory disease capable of producing symptoms ranging from those similar to a common cold, through to very severe or even fatal disease.

The wellbeing of our staff and patients is of the upmost importance to us, and it is the expectation of The Royal Marsden that all patient‑facing staff have an annual flu vaccination, provided free of charge by the Trust.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Trial Administrator
Senior Clinical Trial Administrator

Royal Marsden • Greater London, Sutton

Remote
GBP 38,000 - 47,000
Clinical Research Nurse
Clinical Research Nurse

Royal Marsden • Sutton

Hybrid
GBP 32,000 - 42,000
Clinical Research Doctor - Lerner Lung & Mesothelioma
Clinical Research Doctor - Lerner Lung & Mesothelioma

Royal Marsden • Sutton

Hybrid
GBP 67,000 - 69,000
Staff Nurse (Band 6) - Bud Flanagan East
Staff Nurse (Band 6) - Bud Flanagan East

Royal Marsden • Sutton

Hybrid
GBP 46,000 - 54,000
Staff Nurse (Band 6) - Bud Flanagan East
Staff Nurse (Band 6) - Bud Flanagan East

Transformation Unit • Sutton

Hybrid
GBP 46,000 - 54,000
Advanced Nurse Practitioner
Advanced Nurse Practitioner

Royal Marsden • Greater London

Hybrid
GBP 56,000 - 68,000
Development opportunities
Ongoing professional courses
Flexible working arrangements
+1
Clinical Research Administrative Assistant Apprentice
Clinical Research Administrative Assistant Apprentice

Royal Marsden • Greater London

Hybrid
GBP 27,000 - 33,000
Staff Nurse (Band 6) - Wiltshaw Ward
Staff Nurse (Band 6) - Wiltshaw Ward

Royal Marsden • Greater London

On-site
GBP 36,000 - 48,000
Clinical Practice Educator
Clinical Practice Educator

Royal Marsden • Greater London

On-site
GBP 32,000 - 42,000
Embassy Patients Coordinator
Embassy Patients Coordinator

Royal Marsden • Greater London

Remote
GBP 22,000 - 28,000