Clinical Study Coordinator

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* 4,000 professionals, 0 days wasted, 1 incredible purpose. Together, we are beating cancer.
*** Clinical Study Coordinator**   £30,000 - £34,000 plus
*
* Reports to:

** Clinical Operations Manager   
** Directorate:
** Research & Innovation   
*
* Contract:

** 2 year Fixed Term Contract   
*
* Hours:

** Full time 35 hours per week   
*
* Location:

** Stratford, London Office-based with high flexibility (1-2 days per week in the office)   
** Closing date:
** 1st March 23:55pm
** 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.
** Recruitment process:
** Competency based interview via Microsoft Teams + Task
** At Cancer Research UK, we exist to beat cancer.
** Cancer Research UK are looking for a Clinical Study Coordinator to join our Centre for Drug Development (CDD).CDD is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. 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.

The Clinical Study Coordinator will aid in the development of new cancer therapies by supporting the exploratory, pre-clinical, set-up, monitoring and archiving aspects of clinical trials in accordance with Cancer Research UK Standard Operating Procedures (SOPs) and policies, ICH GCP guidelines (International Conference on Harmonisation-Good Clinical Practice), European Union Directives, UK legislations and other regulatory requirements.

This is a great opportunity for a proactive, diligent and organised individual to gain experience in a clinical trial facility. You may be a clinical trial administrator looking for your next step or already be working at coordinator level but looking to move into an environment with patience benefit at it’s heart. Whatever your background as long as you can demonstrate experience within a busy administrative role, which includes data handling and tracking as well as basic knowledge of ICH/GCP we would love to hear from you.

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.
* Support project teams by coordinating internal and external meetings, including preparation of presentations, Quality Control checking eTMF documents and taking minutes as required.
* Support clinical trial set up activities by creating/maintaining clinical trial files, including Trial Master Files (TMFs), Investigator Trial Files (ITFs), Pharmacy Files (PF), Laboratory Files, and in-house electronic files, and preparing start up documents in conjunction with the Clinical Study Manager (CSM) and Clinical Research Associate (CRA).
* Ensure Trial Master Files (TMFs) are audit ready by performing regular filing and coordinating TMF reviews so that discrepancies are quickly and appropriately addressed.

Order and distribute essential documents such as protocols, investigator brochures, and clinical study reports to investigational sites, maintaining recipient logs/trackers to ensure availability of current documentation.

Experience of providing administrative support in a fast-paced, deadline driven environment.

Some knowledge of Good Clinical Practice, EU clinical trial legislation and the UK clinical research environment.

Experience of collecting, handling and tracking data.

Experience in eTMF (trial master files) would be extremely beneficial.

Working knowledge of ICH/GCP.  with the ability to take initiative Organised with the ability to multi-task, prioritise and work collaboratively within a team. If you’reexperience we’d still love to hear from you. interested in applying and excited about working with us but are unsure if you have the right skills and 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
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