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United Kingdom (UK) 🛡️ UK Work Eligibility 💼 Company - Public
RDL Scientific - Research Tissue Bank Coordinator
RDL Scientific ✓ Verified Employer

Research Tissue Bank Coordinator

Verified Base Compensation
£28,000 - £28,000 / year
£2,333 - £2,333 / mo Apply Now →
Official Specifications

Role Overview & Mandate

Executive Summary

RDL Scientific are looking for an enthusiastic full-time Research Tissue Bank Coordinator to join our dedicated Recruitment Team, which focuses on...

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RDL Scientific are looking for an enthusiastic full-time Research Tissue Bank Coordinator to join our dedicated Recruitment Team, which focuses on the recruitment, retention, and delivery of participants into clinical trials and Experimental Medicine studies at a leading Clinical Trial Unit (CUC) based in Cambridge.

This exciting position offers the opportunity to both oversee the Research Tissue Bank participant cohort and deliver, as part of the team, the focused recall studies.

The Research Tissue Bank Coordinator will be accountable for maintaining, growing and utilising the RTB from initial identification and recruitment of suitable volunteers through to re-contacting consented participants to invite them back to the CUC for further characterisation, such as by venepuncture. They may also be involved in the recruitment and delivery of participants to other trials and studies within the CUC. They will be responsible for creating a welcoming environment for our participants, ensuring they are always treated with dignity, privacy, and safety as they are our number one priority.

Responsibilities

  • Facilitate all matters related to participant recruitment, screening, enrolment and consenting into the RTB.
  • Proactively liaise with all departments to identify and recruit participants into the RTB or other studies based on required selection criteria.
  • Increase the size of the RTB through specific Recruitment Drives, engaging with the Marketing Coordinator and providing input into recruitment campaigns and advertising.
  • Provide general administration support as required, e.g., arrangement of volunteer appointments, organizing transport as required etc
  • Ensure the local study procedures and operations follow HRA, ICH, GCP, GLP, ethical, regulatory, and legal guidelines, relevant SOPs, and company policies.
  • Be familiar with Informed Consent Forms (ICF) and know which ICF is suitable for each category of participant
  • Perform the efficient and safe collection of low interventional biological samples (which may include but are not limited to blood, saliva, urine) from participants including accurate labelling and management.
  • Perform low interventional procedures and clinical assessments including but not limited to, ECG’s, vitals, spirometry, venepuncture according to protocol requirements.
  • Collect and record clinical data accurately, consistent with company policy, legal and regulatory requirements.
  • Perform data management activities including maintenance of all related recruitment documentation and the high quality tissue inventory.
  • Collate metrics and focus on key performance indicators such as participant enrolment/retention figures.

The Ideal candidate will possess and demonstrate these qualities

  • Well-developed communication (written and oral) and numerical skills
  • Ability to work well independently and as part of a team
  • Ability to maintain and promote relationships
  • Adaptability and agility to handle diverse, time-sensitive workloads
  • Excellent organization skills, and ability to complete detailed work accurately and quickly
  • Ability to learn computer programs, databases, and scientific applications
  • Strong analytical skills and balanced judgment

Qualifications

  • Degree in Life Sciences or health-related field
  • Nursing or Healthcare Assistant qualification
  • Immediate Life Support/Basic Life Support certified
  • Possess an understanding of ethical, regulatory, and legal requirements such as ICH, HTA, HRA, GCP.
  • Experience working in a clinical research environment or in health screening
  • Experience in a healthcare environment. e.g., nurse, healthcare assistant, lab assistant/technician, phlebotomist
  • Phlebotomy skills

Job Types: Full-time, Permanent

Salary: From £28,000.00 per year

Benefits:

  • Company pension
  • Life insurance
  • Private medical insurance
  • Sick pay

Ability to commute/relocate:

  • Cambridge, Cambridgeshire: reliably commute or plan to relocate before starting work (required)

Experience:

  • Phlebotomy: 1 year (preferred)

Work authorisation:

  • United Kingdom (required)

Work Location: One location

Reference ID: RTBC

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Compensation Analytics

Estimated Take-Home Pay

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Projected statutory deductions based on standard single-filer baseline tax regulations in the United Kingdom corridor.

Gross Annual Package £28,000 - £28,000
Est. Income Tax Band 20% Basic Rate Band
Statutory Insurance / FICA 8% Class 1 National Insurance (NI)
Estimated Monthly Net £1,867 - £1,820 / mo
Regional Economics

Cost of Living (Cambridge, East of England, England)

Bureau Data
Est. Rent (1-Bed)
£1,100 - £1,750
Monthly Utilities
£140 - £210
Cost Index
112.5
Disposable Tier
Top 15% Rank
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Compliance Standards

Work Authorization Framework

Verified Status: UK Work Eligibility
Corridor: UK Employment Corridor
🛡️ Zero Fee: Direct corporate recruitment with zero placement charges.

Candidate Selection Pipeline

Direct Corridor Track
01
Direct Apply

Submit verified credentials & CV.

02
HR Screening

2-4 day credential verification.

03
Technical Panel

In-depth domain & team interview.

04
Official Offer

Corridor contract & relocation.

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