Clinical Research Specimen Processing Co-ordinator
London: Sarah Cannon Research Institute
Full time 37.5 hours per week
Permanent
Salary: Competitive
We’re recruiting for a Clinical Research Specimen Processing Co-ordinator, to join our Sarah Cannon Research Institute UK team. The Sarah Cannon Research Institute (SCRI) is a world-leading clinical trials facility specialising in the development of new therapies such as targeted and precision medication for cancer patients, our clinical trial portfolio is expanding and we are currently an seeking an experienced highly motivated individual to provide support to our onsite laboratory.

As a Clinical Research Specimen Processing Co-ordinator, you will be an integral member of staff providing technical support to the wider clinical research team for effective service delivery. Main duties of the role will include:

• Handling, processing and shipping of blood/tissue samples in accordance with GCP, HTA, study protocol and local SOPs.
• Inventory management: ordering of lab supplies and destruction of expired kits
• Support the wider team with study set-up and study amendments, ensuring the smooth running of the trial.
• Liaise with clinical and research teams to coordinate sample collection and processing timelines
• Produce and maintain accurate trial documentation, ensuring timely filing, bookings, auditing and reporting
• Management of PK samples
• Temperature monitoring and tracking
• Supporting resolution of Sponsor queries relating to sample processing
• Mentor and support junior team members
• Ensure compliance with safety and quality assurance protocols

At HCA UK we care about what you care about. We care that you want to deliver the very best care. We care that you want a career you can be proud of. We care that you want working conditions that support your health and wellbeing. Let us care for you and your career, the same way you do for others.

• Handling, processing and shipping of blood/tissue samples in accordance with GCP, HTA, study protocol and local SOPs.
• Inventory management: ordering of lab supplies and destruction of expired kits
• Support the wider team with study set-up and study amendments, ensuring the smooth running of the trial.
• Liaise with clinical and research teams to coordinate sample collection and processing timelines
• Produce and maintain accurate trial documentation, ensuring timely filing, bookings, auditing and reporting
• Management of PK samples
• Temperature monitoring and tracking
• Supporting resolution of Sponsor queries relating to sample processing
• Mentor and support junior team members
• Ensure compliance with safety and quality assurance protocol