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Senior Clinical Research Data Manager in Salford

Job in Manchester, Greater Manchester, M9, England, UK
Listing for: Energy Jobline CVL
Full Time position
Listed on 2026-09-11
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 49387 - 56515 GBP Yearly GBP 49387.00 56515.00 YEAR
Job Description & How to Apply Below
Position: Senior Clinical Research Data Manager in Salford, Greater

Job Title:

Senior Clinical Research Data Manager

Location:

Salford Quays

Salary: £49,387- £56,515 per annum - Band 7

Contract:

Full time, Permanent

About the Role

The Haemophilia Database (NHD) is the UK's registry for people with inherited and acquired bleeding disorders, collecting clinical and treatment data from NHS haemophilia centres across the UK.

We are seeking an experienced Senior Clinical Research Data Manager to provide specialist data management and coordination for post-marketing studies, investigator-initiated studies and other approved research delivered through the NHD.

Working with clinicians, NHS haemophilia centres, researchers and external study partners, you will translate study protocols and research questions into practical data-collection requirements. This will include developing study-specific Case Report Forms (CRFs), database modules, worksheets, data management plans and completion guidance.

You will also be a key operational contact for participating centres, helping sites meet study requirements and ensuring research data are complete, accurate, timely and suitable for analysis and reporting.

The role covers three main areas
  • Clinical research data management - developing study data-collection tools and processes and coordinating data review, cleaning, validation and query resolution.
  • Site coordination and training - supporting participating NHS centres and providing practical guidance and training on study requirements and data submission.
  • Research governance and quality - ensuring study data management meets applicable research governance, data protection, consent and quality‑assurance requirements.

You will join the established UKHCDO/NHD multidisciplinary team, working alongside data managers, data scientists, statisticians and clinicians, and with external partners including pharmaceutical companies and Clinical Research Organisations (CROs).

Key Responsibilities Clinical Research Data Management

You will:

  • Lead the design, review, piloting and implementation of paper and electronic CRFs, worksheets and study‑specific data‑collection tools.
  • Translate study protocols, endpoints and research questions into proportionate, clinically meaningful data fields and collection processes.
  • Develop and maintain data management plans, data dictionaries, CRF completion guidance and associated documentation.
  • Coordinate the collection, entry and verification of clinical research data from participating sites.
  • Review data for completeness, consistency and accuracy, managing data cleaning and query resolution.
  • Monitor data quality, completeness, timeliness and site performance.
  • Support the development and maintenance of NHD databases and study‑specific modules, recommending improvements to systems and processes.
Site Coordination and Training

You will act as a principal operational contact for participating centres, building effective relationships with Haemophilia Centre Medical Directors, Research Nurses, Data Managers and other clinical and research staff.

You will establish practical data‑collection arrangements, provide training and guidance on study requirements and CRF completion, respond to operational and system queries, and work collaboratively with sites to overcome barriers to high‑quality and timely data collection.

You will also liaise with external study partners and CROs, attend relevant study meetings and coordinate agreed actions.

Research Governance and Quality

You will apply a sound working knowledge of UK research governance, HRA and Research Ethics Committee requirements, Good Clinical Practice (GCP) and sponsor responsibilities.

You will ensure appropriate compliance with UK GDPR, the Data Protection Act 2018 and NHS information‑governance requirements, maintaining…

Position Requirements
10+ Years work experience
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