Clinical Data Manager

Clinical Data Manager
£39,000 – £44,000 plus benefits

Reports to: Data Management Operations Manager
Directorate:  Research & Innovation
Contract:  24-month Fixed Term Contract
Hours: Full time, 35 hours per week or a 4 day week of 28 hours.
Location: Stratford, London (high flex 1-2 days per week) or home based, UK (at request).  
Closing date: Sunday 30th August 23:55pm
Interview date: Approximately w/c 14th September
Recruitment process: Competency based interview via Microsoft Teams + Data Management Task

Visa sponsorship: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship. 

At Cancer Research UK, we exist to beat cancer.

Cancer Research UK (CRUK) are looking for a Clinical Data Manager to join our team within our Centre for Drug Development (CDD) on a 24 month fixed term contract.

CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in. It is an exciting time for CDD as we’re expanding our teams to move forward with an ambitious new strategy to maximise the impact of our research to benefit patients. Several teams are hiring new roles to make this new strategy a reality, expanding the size of our project portfolio and bringing in new skills as we work more internationally.

This is a great opportunity for an experienced Clinical Data Manager, with a keen interest in the field of Oncology, to join a small team made up of 8 Data Management professionals. This will allow you to work on DETERMINE, our multi-drug, precision medicine platform trial in rare cancers, recruiting both adults and children.

 
What will I be doing?

• Lead the data management of assigned arms of the DETERMINE trial.

• Review the clinical trial data ensuring that data cleaning is managed effectively and efficiently, highlighting any issues that may affect data quality.

• Manage the development or amendment of clinical trial databases, reviewing eCRFs, specifying edit checks and performing validation.

• Facilitate the reporting of the data by managing the specification and validation of data listings and tables, coding adverse event terms and reconciling serious adverse events.

• Monitor the status of data entry and data cleaning, locking data when appropriate to protect data integrity.

• Work to achieve key performance indicators and project goals.

What are we looking for?

• You will be a biomedical science graduate, hold a nursing qualification or have equivalent relevant experience.

• Proven knowledge and understanding of clinical data management and drug development, working to ICH/GCP and relevant legislation.

• Good knowledge and previous use of an electronic data capture (EDC) clinical trial database.

• Excellent written and verbal communication skills.

• Excellent attention to detail whilst retaining sight of the bigger picture.

• Good planning and organisational skills, able to prioritise and manage multiple competing tasks whilst working to challenging timelines.

• In addition, experience of working on oncology trials would be desirable.

Our organisation values are designed to guide all that we do.

Bold: Act with ambition, courage and determination  

Credible: Act with rigour and professionalism   

Human: Act to have a positive impact on people  

Together: Act inclusively and collaboratively

We’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.

If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience, we’d still love to hear from you.

What will I gain?

We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.

You can explore our benefits by visiting our careers web page.

How do I apply?

We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively.

For more information on this career opportunity please visit our website or contact us at [email protected].    

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