CrawlJobs Logo

Clinical Compliance Manager

United Kingdom, Leicester Employment contract 69080.00 - 73585.00 GBP / Year · Job Posted June 15, 2026
Apply Position
Job Link Share

Job Description

At Prime Life, we are committed to delivering outstanding, person-centred care across our nursing homes. We are now looking for an experienced and passionate Clinical Compliance Manager to join our team and play a pivotal role in ensuring our services meet and exceed regulatory standards. This is a dynamic, multi-site role where you will work closely with Home Managers, clinical teams, and senior leadership to drive compliance, improve quality, and support the delivery of safe, effective, and high-quality care.

Job Responsibility

  • Support services to meet and maintain CQC Fundamental Standards and relevant legislation
  • Drive improvements to achieve Good and Outstanding CQC ratings
  • Interpret and implement regulatory updates across all homes
  • Provide expert compliance guidance to managers and clinical teams
  • Embed strong clinical governance frameworks across services
  • Oversee standards in medication management, infection control, safeguarding, and care planning
  • Monitor key clinical indicators including falls, pressure ulcers, and incidents
  • Promote consistently high standards of person-centred care
  • Lead and support a robust programme of clinical audits and quality checks
  • Carry out regular site visits to assess performance and compliance
  • Support homes through CQC inspections
  • Analyse audit outcomes and implement improvement plans
  • Identify and manage clinical and compliance risks
  • Support investigations into incidents, complaints, and safeguarding concerns
  • Lead or contribute to root cause analysis (RCA) and corrective action plans
  • Maintain and escalate risks through appropriate governance channels
  • Coach and support Home Managers and nursing teams on compliance standards
  • Ensure clinical staff meet training and competency requirements
  • Provide on-call clinical support when required
  • Promote a culture of continuous learning and professional development
  • Produce compliance reports and track KPIs and quality metrics
  • Ensure clinical documentation meets regulatory standards
  • Work collaboratively with internal teams and support external inspections
  • Share best practice and drive continuous improvement across services

Requirements

  • Registered Nurse (RGN/RMN) with active NMC registration
  • Significant experience within a nursing home or clinical care setting
  • Strong understanding of CQC standards and inspection processes
  • Experience in clinical governance, compliance, or quality roles
  • Proven experience conducting audits and implementing improvement plans

Nice to have

  • Leadership or management qualification
  • Experience supporting services through CQC inspections
  • Background in multi-site care environments

What we offer

  • Competitive salary
  • Company car contribution, fuel card, phone, and laptop
  • A rewarding role with real impact on care quality
  • Opportunity to work across a diverse portfolio of homes
  • Supportive leadership and collaborative culture
  • Ongoing professional development

Looking for more opportunities?

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

Similar Jobs for

Clinical Compliance Manager

8 matching positions

Clinical Compliance Manager

Clinical Compliance Manager for nursing care homes within the Brighton area. A c...
Location
Location
United Kingdom , Brighton and Hove
Salary
Salary:
60000.00 GBP / Year
compass-associates.com Logo
Compass Associates
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Qualified RGN or RMA
  • Proven experience in clinical compliance, audit, governance or senior clinical lead roles within care homes
  • Strong knowledge of CQC criteria, KLOEs and related legislation
  • Excellent attention to detail and ability to drive continuous improvement
Job Responsibility
Job Responsibility
  • Maintaining the highest standards of clinical compliance
  • Supporting CQC readiness
  • Leading audits
  • Policy development
  • Risk management
  • Ensuring regulatory excellence across the home
  • Fulltime
Read More
Arrow Right

R&D Clinical - Quality Compliance Senior Manager

We are hiring a R&D Clinical Quality Compliance Senior Manager, who will operate...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s Degree in appropriate discipline e.g. Life Sciences, Medical
  • 15-18 years’ experience working in Biotech, Pharmaceutical or CRO company
  • In-depth knowledge of ICH GCP
  • Extensive experience in Quality Management, Quality Assurance, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality and quality by design are core responsibilities
  • Experience using electronic QMS such as Veeva Vault and eTMF
  • Experience and understanding of Clinical R&D activities and Global Regulations
  • In-depth knowledge of the Regulatory Submission and Inspection readiness, preparation and management procedures
  • Extensive experience in Quality Oversight of Clinical Trials, including clinical trial protocol development and execution
  • Strong verbal and written communication skills, including strong business writing abilities and active listening
  • Strong analytical, critical-thinking, and decision-making abilities
Job Responsibility
Job Responsibility
  • Key advisor to the study team throughout the clinical trial life cycle, providing independent and objective quality input in the areas of GCP and compliance with Amgen SOPs and processes
  • Review and provide input into the development of the initial clinical study protocol and subsequent amendments, with focus on quality by design, confirming it’s fit for purpose, clear, concise and consistent
  • Actively provide input into study risk assessment activities
  • Review and provide input into other key study documents and plans
  • Direct study teams through the management of complex quality issues
  • Participate in key activities related to Risk Based Quality Management
  • Using available tools, analyze quality data metrics
  • Monthly meetings with study team lead/associate director, to review the following: on-going quality issues, quality trends, program filing timelines, inspection readiness, potential inspections and audit scheduling and planning and any other topics deemed relevant
  • Support the clinical study team with inspection readiness activities
  • Support continuous improvement initiatives within TA Quality
What we offer
What we offer
  • Varied opportunities to learn, develop, and move up and across our global organization
  • Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
  • Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
  • Flexible work arrangements
  • Fulltime
Read More
Arrow Right

Clinical Compliance and Improvement Manager

You will drive clinical compliance and continuous improvement for assigned Devel...
Location
Location
United States , Philadelphia, Pennsylvania
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in life sciences, clinical research, medicine, pharmacy, or equivalent experience
  • 3 plus years of clinical operations experience supporting study delivery
  • Experience with ICH Good Clinical Practice (GCP) and applicable regulatory requirements
  • Experience in Global Monitoring and Site Engagement
  • Experience with compliance monitoring, audits, or inspection preparation in clinical settings
  • Experience leading investigations and drive corrective and preventive actions to closure
Job Responsibility
Job Responsibility
  • Lead/contribute to risk proportionate compliance monitoring activities and local monitoring deliverables to identify quality gaps and operational risks
  • Drive investigations and analysis, lead and support root cause analysis, and help define corrective and preventive actions
  • Partner with R&D Quality and Risk colleagues on inspection readiness and regulatory expectations
  • Track trends and metrics, translate findings into clear action plans, and measure outcomes
  • Coach clinical teams to embed sustainable quality practices and improve ways of working
  • Lead and contribute to continuous improvement activities and cross-functional projects that simplify processes and raise operational standards
  • Build strong working relationships with assigned Development Operations teams and stakeholders
  • Drive compliance with GCP, regulatory/legal requirements and GSK written standards
  • Ensure that issues and operational challenges are appropriately identified, managed, addressed and communicated in the assigned Development Operations team(s)
  • Collaborate closely with the R&D Quality & Risk Management organization to share information on potential risk areas and obtain insights into risks that require mitigation by Development Operations
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Fulltime
Read More
Arrow Right

Global Trade Compliance Manager - Sanctions Screening and Clinical Valuation Lead

In this role, you will serve as the global screening lead responsible for execut...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree and 4 years of experience in compliance or screening operations, risk management, regulatory affairs, audit, law, or a related field
  • OR Associate's degree and 8 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field
  • OR High school diploma / GED and 10 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field
Job Responsibility
Job Responsibility
  • Serve as subject matter expert on OFAC 50% Ownership aggregation principles and BIS 50% Entity List alignment requirements
  • Conduct enhanced due diligence on counterparties to determine ultimate beneficial ownership (UBO)
  • Aggregate ownership interests across direct and indirect shareholders to assess sanctions exposure
  • Screen vendors, customers, banks, and other counterparties against OFAC SDN List, BIS Entity List / Military End User Lists, and other applicable restricted party lists
  • Review, analyze, and adjudicate screening alerts
  • determine true matches vs. false positives
  • Identify hidden or indirect sanctioned ownership exposure
  • Gather and interpret information from public records, corporate registries, databases, and commercial screening tools
  • Develop comprehensive case files documenting findings, risk assessments, and recommended actions
  • Prepare clear, well-supported investigative reports for leadership and Legal review
  • Fulltime
Read More
Arrow Right

Senior Manager, Clinical Operations/ Senior Global Trial Manager - FSP

Parexel are currently recruiting for an experienced Global Study Operations Mana...
Location
Location
Italy; United Kingdom , Remote; Remote
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7 years of relevant clinical trial management experience
  • Global trial management experience is essential
  • Experience managing CRO outsourced studies is essential
  • Excellent leadership, communication, and organizational skills
  • Able to multi-task under limited direction and on own initiative
  • M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential
  • Prior and demonstrable experience working at a senior level within Study start up preferred
Job Responsibility
Job Responsibility
  • Accountable for the end-to-end clinical trial delivery
  • Providing operational leadership and oversight of cross-functional deliverables
  • Leading a cross functional trial team to build and deliver the trial operational plan
  • Responsible for leading the Cross functional trial team to influence and execute delivery of the operational plan and for end-to-end trial execution
  • Accountable for overall trial delivery, budget, timelines, quality, and milestones
  • Oversight of all aspects of CRO/vendor identification, set up, statement of work creation, budget oversight and performance (KPI’s and metrics)
  • Proactively ensure that trial deliverables and milestones are met according to corporate and study-level goals
  • Identify risks and ensure mitigations and contingencies are being initiated and followed through
  • Ensure trial Is operationalized in compliance with global health authority regulations and guidelines and internal operating procedures and processes
  • Participate in preparation for, and conduct of, Health Authority Inspections and internal QA audits
Read More
Arrow Right
New

Registered Home Manager (Clinical)

Registered Care Home Manager - Nurse Required. Barrington Lodge - Bishop Aucklan...
Location
Location
United Kingdom , Bishop Auckland
Salary
Salary:
55000.00 GBP / Year
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of three years experience as a Home Manager
  • Qualified Home Manager who has managed a minimum of a 70 bedded home specializing in the care of Dementia and General Nursing
  • Experience in leading and managing teams within a Person-centered Care environment
  • Strong Operational background
  • Able to evidence CQC Compliance published rated good in the last 3 years
  • Level 5 in Leadership Management
  • Experienced in caring for older people
  • Capable and confident leader with the drive and interest to grow and shape a team
  • Experienced in managing a successful home or services in healthcare
  • Confident in your knowledge of CQC regulations
Job Responsibility
Job Responsibility
  • Develop and sustain the Home
  • actively leading and supporting your team to deliver the highest standards of care for our residents
  • Build effective relationships with your team, residents, their relatives, and the local community
What we offer
What we offer
  • Discounts on Shopping, Fashion, Days out, Travel, Entertainment and lots more
  • FREE face-to-face counselling, for you and your family
  • Staff recognition award ceremonies
  • £30 voucher available every month for the nominated ‘Employee of the month’
  • Opportunities for training and career progression
  • Salary Sacrifice Pension scheme
  • Blue Light Card – up to 50% discount across 100’s of retailers
  • Access to a FREE eye test and discounted glasses
  • Cashback card – save up to £500 annually, can be used at over 80 big brands
  • Wellbeing portal: FREE meditation series, FREE wellbeing podcasts & live virtual events, FREE mental health support programmes, FREE workout plans, FREE Live digital gym classes, FREE mindset and wellbeing series
  • Fulltime
Read More
Arrow Right
New

Behavioral Health Responder- Clinical Manager

The Department of Campus Safety’s Manager of the Community Behavioral Health Res...
Location
Location
United States , Denver
Salary
Salary:
90000.00 - 95000.00 USD / Year
du.edu Logo
The University Of Denver
Expiration Date
July 09, 2026
Flip Icon
Requirements
Requirements
  • Independent clinical licensure in the state of Colorado (LCSW, LPC, LMFT, or Licensed Psychologist).
  • Master’s in counseling, psychology, social work or other related fields from accredited program
  • Experience supervising a team
  • Experience in crisis intervention and suicide prevention
  • Knowledge of HIPAA compliance, 42 CFR Part 2, relevant behavioral health statutes, and rules and regulations relative to confidentiality.
  • Must have a valid drivers license
  • Must be able to work long periods of time in variable inside and outside conditions.
  • Must be willing to work as needed, including nights, weekends or holidays.
  • Must be able to make impactful, independent decisions without direct supervisory oversight.
  • Must be able to complete and maintain P1 Aid, CPR, Narcan and tourniquet training and professional certifications in personal defense required of CAPS clinicians.
Job Responsibility
Job Responsibility
  • Develop standard operating procedures for behavioral health response program
  • Develop key relationships and partnerships across the University of Denver campus
  • Coordinate appropriate staffing for program operations
  • Regularly evaluate program operations and provide recommendations for strategic planning.
  • Provide direct supervision to all clinical staff and clinical student interns.
  • Maintaining accurate and timely confidential documentation.
  • Provide in-person and/or telehealth crisis outreach, crisis de-escalation, clinical risk assessment and level of care assessments when indicated to DU community, its affiliated and local community members.
  • Provide follow up outreach and resources to individuals who received contact from the Behavioral Health Response program.
  • Serve on the DU CARE team and provide consultation on individuals of concern.
  • Facilitate critical incident debriefs for Department of Campus Safety staff or other DU divisions upon request.
What we offer
What we offer
  • medical
  • dental
  • retirement
  • paid time off
  • tuition benefit
  • ECO pass
  • Fulltime
Read More
Arrow Right

Manager Clinical Services Home Health

At CHI Franciscan Health at Home, we strive to embody our mission of delivering ...
Location
Location
United States , University Place
Salary
Salary:
45.26 - 74.67 USD / Hour
americannursingcare.com Logo
American Nursing Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Current RN license (BSN preferred) or Therapist in good standing
  • CPR or BLS certification (current)
  • Two years of home care or hospice experience
  • one year in hospital nursing preferred
  • Strong clinical skills and understanding of home care regulations
  • Excellent written and verbal communication skills
  • Ability to work collaboratively within a multidisciplinary team
  • Demonstrated leadership and supervisory skills, with attention to detail and organizational abilities
Job Responsibility
Job Responsibility
  • Contribute to the delivery of high quality care by ensuring the coordination, continuity, and quality of clinical care follows a physician's approved plan of treatment
  • Facilitate the completion of documentation to comply with regulatory, operational and financial requirements
  • Act as a clinical resource to internal and external customers
  • Operate with limited supervision
  • Promote and support departmental and organizational decisions
  • Act as a Clinical Educator when needed
  • Utilize Homecare Homebase to accurately document patient interactions, assessments, and care plans
  • Train and mentor clinical staff in effective EMR documentation practices
  • Participate in case conferences and in-service training
  • Direct the delivery of accurate and timely client care in compliance with regulations
What we offer
What we offer
  • Generous annual bonus opportunity based on company performance
  • Excellent holiday and paid time off plans
  • Medical, dental, and vision plans
  • Tuition reimbursement for degree-seeking students
  • Employer contribution to your 401(k)
  • Health/dental/vision
  • FSA
  • Matching retirement plans
  • Paid time off
  • Tuition assistance
  • Fulltime
Read More
Arrow Right