CrawlJobs Logo
Sheffield Children's NHS Foundation Trust Logo Sheffield Children's NHS Foundation Trust · Nursing

Clinical Research Facility Manager

United Kingdom, Sheffield Employment contract 49387.00 - 56515.00 GBP / Year · Job Posted May 04, 2026
Apply Position
Job Link Share

Job Description

We are looking for an experienced and motivated Clinical Research Facility (CRF) Manager to lead the Research Delivery team at Sheffield Children's. You will help deliver a range of clinical research studies--from first-in-human Phase 1 trials to observational registry studies--across multiple specialties. You'll ensure high-quality care for young participants and help shape the future of paediatric healthcare through the latest research.

Job Responsibility

  • Lead the daily operations of the Clinical Research Facility and Research Delivery team
  • Oversee the full lifecycle of clinical trials--from set-up to close-out
  • Collaborate with partners including Trial Sponsors and CROs
  • Ensure standards of care for children and young people participating in research
  • Support the professional development of the Research Delivery team

Requirements

  • Registered nurse on relevant part of the register (ideally RSCN/RN Child)
  • Masters Level Degree in healthcare subject or equivalent level of experience
  • Evidence of ongoing professional development
  • Research qualification (GCP)
  • Leadership and management experience or proven ability to provide leadership and management to a team
  • Experience of line management, clinical supervision or mentoring
  • Significant experience of clinical trials administration and/or management
  • Experience of dealing with colleagues from a wide range of backgrounds and at all levels
  • Logical and consistent work and career pattern
  • Experience of taking a lead role in the set up and running of complex interventional research in the NHS to include the coordination of site visits and liaising with Sponsors and monitors
  • Experience of preparing Standard Operating Procedures
  • Partnership working across NHS - academic organisations and experience of working with commercial Sponsors of research
  • Recent NHS experience
  • IT systems and packages
  • R&D policy and current NHS R&D priorities
  • Demonstrable in depth knowledge of the Research Governance Framework (RGF), the Clinical Trials Regulations and ICH GCP
  • Evidence of ability to help / support junior staff
  • Research activity and management in the NHS or academic sector
  • Clinical skills including ability to perform ECG and cannulate
  • Numerate
  • IT literate
  • Excellent attention to detail
  • Ability to motivate others
  • Excellent time management - able to plan and work to tight timescales and to multi-task effectively
  • Strategies for delivering studies to time and target
  • Awareness of the High Level Objectives of the NIHR and research KPIs
  • Excellent interpersonal skills, including written and verbal communication skills

Nice to have

  • Management/leadership qualification
  • Assessing and mentoring qualification
  • Training in recruitment and selection of staff
  • Experience of working in a clinical capacity with children
  • Budget management including the costing of commercial trials and non-commercial grants
  • Experience of writing SOP's
  • Advanced clinical skills
  • Project Management skills (Microsystems or similar)

What we offer

  • Generous annual leave and pension schemes
  • Health and wellbeing programmes
  • Exclusive discounts
Sheffield Children's NHS Foundation Trust - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Clinical Research Facility Manager

8 matching positions

New

Clinical Research Associate II

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
  • Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
  • Sound problem solving skills
  • Able to take initiative and work independently
  • Advance presentation skills
  • Client focused approach to work
  • Ability to interact professionally within a client organization
  • Flexible attitude with respect to work assignments and new learning
  • Ability to prioritize multiple tasks and achieve project timelines
  • Willingness to work in a matrix environment
Job Responsibility
Job Responsibility
  • Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites
  • Build relationships with investigators and site staff
  • Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements
  • Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up
  • Address and resolve issues at sites
  • Follow-up on and respond to appropriate site related questions
  • Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues
  • Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections
  • Collect, review, and approve updated/amended site documentation
  • Evaluate site recruitment plan in collaboration with the site staff
Read More
Arrow Right
New

Clinical Research Coordinator II

Must be comfortable with 50% travel. Highly prefer someone who lives in the Nort...
Location
Location
United States
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
  • Critical care, nephrology and/ or cardiac experience desirable
  • Willing to pursue CCRC or CCRP certification when eligible
  • Current state licensure, if applicable
  • Good computer skills: Microsoft Office minimally
  • Excellent communication and organizational skills
  • Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role
Job Responsibility
Job Responsibility
  • Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
  • Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
  • Protect the rights and the well-being of subjects enrolled in studies
  • Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
  • Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
  • Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
  • Accurately documents study subject activities as outlined by the protocol
  • Maintains documents according to applicable HIPAA and regulatory requirements
  • Implements study-specific quality goals and practices
  • Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance
Read More
Arrow Right

Senior Clinical Research Associate (Oncology Experience Required)

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United Kingdom
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
  • Minimum of 5 years' experience in CRO or Pharma trials environments
  • Experience in oncology trials and RECIST criteria is essential
  • Fluency in English is required
  • Proficiency in local language is required
  • Networking and relationship building skills
  • Ability to communicate effectively and appropriately with internal and external stakeholders
  • Ability to adapt to changing technologies and processes
  • Excellent communication (verbal and written), presentation, and interpersonal skills
  • Identifies and builds effective relationships with investigator site staff and other stakeholders
Job Responsibility
Job Responsibility
  • Ensuring regulatory, ICH-GCP and protocol compliance
  • Verifying the process of obtaining informed consent
  • Assessing factors that might affect subject safety and clinical data integrity
  • Conducting monitoring activities using different methods (e.g., on site and remote)
  • Conducting source document review and verification
  • Managing reporting of protocol deviations
  • Applying query resolution techniques
  • Performing Investigational Product (IP) inventory, reconciliation and review
  • Verifying IP dispensation and administration
  • Managing reporting of identified issues
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
France , Paris Region
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in oncology trials and RECIST criteria is essential
  • Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
  • Networking and relationship building skills
  • Ability to communicate effectively and appropriately with internal and external stakeholders
  • Ability to adapt to changing technologies and processes
  • Excellent communication (verbal and written), presentation, and interpersonal skills
  • Identifies and builds effective relationships with investigator site staff and other stakeholders
  • Proficiency in local language is required
  • Advanced level or fluency in English is required
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensuring regulatory, ICH-GCP and protocol compliance
  • Verifies the process of obtaining informed consent
  • Demonstrates diligence in protecting the confidentiality of each subject
  • Per the Clinical Monitoring Plan (CMP) or SMP: Ability to conduct monitoring activities using different methods
  • Conducts source document review and verification
  • Manages reporting of protocol deviations and appropriate follow up
  • Applies query resolution techniques remotely and on site
  • May perform Investigational Product (IP) inventory, reconciliation and reviews storage and security
  • Verifies the IP has been dispensed and administered to subjects
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate (Oncology Experience Required) - UK (Remote) - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United Kingdom
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience in oncology trials and RECIST criteria is essential
  • Minimum of 4 years' experience in CRO or Pharma trials environments is also essential
  • Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience
  • Networking and relationship building skills
  • Ability to communicate effectively and appropriately with internal and external stakeholders
  • Ability to adapt to changing technologies and processes
  • Excellent communication (verbal and written), presentation, and interpersonal skills
  • Identifies and builds effective relationships with investigator site staff and other stakeholders
  • Proficiency in local language is required
  • Fluency in English is required
Job Responsibility
Job Responsibility
  • Oversight of Monitoring Responsibilities and Study Conduct
  • Ensuring regulatory, ICH-GCP and protocol compliance
  • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions
  • immediately communicates/escalates significant issues to the project team and develops action plans
  • Verifies the process of obtaining informed consent has been adequately performed and documented
  • Demonstrates diligence in protecting the confidentiality of each subject and assesses factors that might affect subject safety and clinical data integrity
  • Per the Clinical Monitoring Plan (CMP) or SMP: Ability to conduct monitoring activities using different methods (e.g., both on site and remote) where allowed by country regulations
  • Conducts source document review and verification of appropriate site source documents and medical records
  • Verifies required clinical data entered in the Case Report Form (CRF) is accurate and complete
  • Manages reporting of protocol deviations and appropriate follow up
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Advanced Technology
  • Diverse therapeutic areas and project exposure
  • Fulltime
Read More
Arrow Right

Clinical Research Associate II - Multi-Sponsor

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Italy , Milan
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
  • Close to at least 2 years independent monitoring experience in a similar setting
  • Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
  • Sound problem solving skills
  • Able to take initiative and work independently
  • Advance presentation skills
  • Client focused approach to work
  • Flexible attitude with respect to work assignments and new learning
  • Ability to prioritize multiple tasks and achieve project timelines
  • Willingness to work in a matrix environment
Job Responsibility
Job Responsibility
  • Act as PAREXEL's direct contact with assigned sites
  • Build relationships with investigators and site staff
  • Facilitate and support site with access to relevant study systems
  • Evaluate if on-site staff assignment is still accurate
  • Address and resolve issues at sites
  • Follow-up on and respond to appropriate site related questions
  • Apply working knowledge to identify and evaluate potential data quality and data integrity issues
  • Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required
  • Collect, review, and approve updated/amended site documentation
  • Evaluate site recruitment plan
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator I

Supports Frenova Renal Research by providing administrative and clinical support...
Location
Location
United States of America , Mishawaka
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Diploma required
  • Associate’s Degree or Certified Medical Assistant preferred
  • 2-4 years of experience of related experience preferred
  • Minimum 18 months experience in a medical setting and/or clinical research setting required
  • Willingness to obtain research specific training as needed
  • Ability to meet deadlines for multiple concurrent projects
  • Ability to understand and follow study specific protocol and direction
  • Ability to understand a patient medical record
  • Attention to detail required
  • Good computer skills including MS Excel
Job Responsibility
Job Responsibility
  • Utilizes experience and knowledge to act as a resource and provide on-going leadership and support to Clinical Research Assistant I
  • Conducts on the job training for Clinical Research Assistant I as requested
  • Researches and identifies research related issues and discrepancies
  • Obtains and prepares regulatory/essential documents throughout the duration of a study
  • Ensures documents and forms are compiled and submitted in a timely manner
  • Assists with maintaining constant communication with Institutional Review Boards, study sponsors, dialysis facility, practice and field staff
  • Assists with the contracting process, document preparation and execution
  • Interfaces with potential study subjects for the purpose of promoting participation in research studies
  • Assists with screening subjects for participation eligibility
  • Assists with and documents the obtaining of informed consent according to GCP
What we offer
What we offer
  • Healthcare
  • Continuing Education
  • Paid Time Off
  • Collaborative Environment
  • Additional Perks
  • 401(k) Retirement Saving
  • Fulltime
Read More
Arrow Right

Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
Argentina
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 1 year as a clinical monitor with demonstrated experience of monitoring (virtual & onsite)
  • Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
  • Proficiency in local language preferred
  • English is required
  • Sound problem solving skills
  • Able to take initiative and work independently
  • Advance presentation skills
  • Client focused approach
  • Ability to interact professionally within a client organization
  • Flexible attitude
Job Responsibility
Job Responsibility
  • Act as PAREXEL’s direct contact with assigned sites
  • Assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites
  • Perform problem-solving to address and resolve site issues
  • Build relationships with investigators and site staff
  • Facilitate and support site with access to relevant study systems
  • Ensure sites are compliant with project specific training requirements
  • Evaluate on-site staff assignment
  • Address and resolve issues at sites
  • Follow-up on and respond to appropriate site related questions
  • Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right