Clinical Auditor Job at Blackrock Health Hermitage Clinic

GCP Quality Auditor

In this vital role within R&D Quality you will be planning and participating in ...

Location

United Kingdom , Uxbridge; London; Edinburgh; Cambridge; Aberdeen

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Degree educated
Proven and extensive international auditing experience in GCP
Experience of data mining, manipulation and data analytics would be advantageous
Excellent written and verbal communication skills

Job Responsibility

Plan, conduct and report routine and directed GCP compliance audits internationally
Serve as a lead auditor for complex GCP audits
Identify and communicate compliance risks to R&D Quality management
Host and/or play a role in regulatory authority inspections
Contribute to or lead R&D Quality process improvement initiatives
Author and contribute to the development of R&D Quality cross functional controlled documents

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Inpatient DRG Nursing Auditor

Join our team in Manila as Inpatient DRG Nursing Auditor. If you’re a registered...

Location

Philippines , Taguig City

Salary:

Not provided

Access Healthcare LLC

Expiration Date

Until further notice

Requirements

Good Comprehension skills
Strong attention to detail and communication skills
Curious and willing to ask relevant questions
Ability to understand client guidelines related to insurance advantage claims
Must be Philippine Registered Nurse with Active license
Must have an experience in clinical and audit in IP DRG

Job Responsibility

Conduct initial audit reviews to validate billed diagnoses and DRG code are supported by medical records
Record audit results and document finding notes based on policies using professional clinical resources
Perform provider appeals reviews and render decision to either uphold or overturn original finding
Review questionable encoder results, complex cases, and appeal reviews to facilitate referrals to clinical department as needed
Propose new audit concepts supported by your research and analysis
Define new audit concept criteria and test and validate new concepts developed by analytics team
Escalate facility issues per client guidance

New

Quality Coordinator

The key purpose this role is to lead and conduct clinical audits, with the aim o...

Location

Ireland

Salary:

Not provided

Blackrock Health Hermitage Clinic

Expiration Date

Until further notice

Requirements

Clinical background is essential
Qualification in auditing is desirable
Experience with IT / administration systems
Experience in a Quality/ Healthcare environment desirable
Experience working on own initiative and with multidisciplinary stakeholders
It is essential that you have valid work permission for the Republic of Ireland to take up employment for this position, or in the case of critical skills, you must be eligible for a work permit.

Job Responsibility

To conduct clinical audits including but not limited to reviewing charts, other documentation, and observation of practice
Liaise with the Quality and Risk Manager to set up audit schedules and review current audit frameworks
To facilitate clinical audit work across the organisation
Provide advice guidance and support to staff undertaking clinical audit projects
Ensuring that audits comply with the principles of good practice
To work closely with hospital departments in conjunction with the Quality team to provide reports and feedback on audits conducted
Develop an audit and monitor compliance
Validate auditors in line with hospital policy and JCI /HIQA requirements
Review patient records or other data sources and accurately and completely record information in accordance with the audit design and protocols
Maintain strict confidentiality in relation to patient identifiable information

What we offer

Competitive salary
Pension
Discounted café
Sports and Social club
Employee Assistance Programme
Discounted onsite pharmacy

Fulltime

New

Contract Analyst I

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Poland , Warsaw

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in appropriate scientific or business disciplines
Excellent communication skills (both oral and written)
5 years’ experience as contract negotiator in pharmaceutical or CRO side including leading activities and oversight of other negotiators

Job Responsibility

Overseeing a Clinical Research Organization responsible for contract negotiations and prepare, negotiate and finalize agreements and budgets related to clinical trials
Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts
Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator‐initiated studies via oversite of a Clinical Research Organization responsible for contract negotiations
Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required
Participate in discussions related to the development of site/investigator budgets aligned with fair market value
Manage the contract amendment lifecycle
Work with the global CCS team as necessary to review and analyze contractual terms to reach resolution
Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions
Escalate issues as appropriate
Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Director of Quality Assurance, Clinical

Responsible for leading in the development, implementation and maintenance of QA...

Location

United States , Berkeley

Salary:

220000.00 - 235000.00 USD / Year

Caribou Biosciences

Expiration Date

Until further notice

Requirements

Undergraduate or graduate degree(s) in Biological Sciences, Chemistry, or related Science discipline
At least 15 years of experience in clinical quality assurance (GCP, GLP and PV) in cell & gene therapy/biotechnology and/or pharmaceutical industry
Experience working in biologics is strongly preferred
Subject Matter Expert (SME) working knowledge on current interpretation/implementation of United States Code of Federal Regulations, ICH Guidelines and other local government regulatory requirements governing clinical research
Proven track record in developing and implementing quality systems and processes in a clinical setting
Expertise in creating and executing audit plans outlining all service providers (vendor) audits, clinical investigator site audits, CSV audits and process audits
Advanced knowledge of Quality Assurance principles, concepts, industry practices, and standards
Prior GLP experience with quality oversight and auditing studies/vendors (preferred)
Excellent verbal and written communication skills
Ability to lead cross-functional teams and independently prioritize work

Job Responsibility

Compliance Oversight: Ensure that all clinical trial activities comply with guidelines and international regulations (e.g., ICH-GCP and ICH-PV), and applicable laws
Documentation Review: Conduct thorough reviews of study-related documentation, including protocols, investigator brochures, informed consent forms, and CSRs, to verify compliance with GCP requirements
Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams
Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline
Plan and oversee activities in support of regulatory submissions and inspections
Lead GCP Inspection Readiness efforts, ensure implementation and prepare internal and external teams for Pre-Approval Inspections (PAI)
Implement, monitor, and promote best practices of all Quality Assurance Systems to ensure compliance with relevant FDA, EU and ROW regulations/directives/requirements and ICH guidelines
Quality Management System (QMS): Maintain and enhance Caribou’s QMS by implementing processes and procedures that ensure consistent adherence to GCP, GLP and PV standards throughout the clinical trial lifecycle
Develop and implement the appropriate suite of Standard Operating Procedures (SOPs), quality manuals, policies, and other related quality documents
Ensure that these systems are effectively communicated, understood, and followed by relevant stakeholders

What we offer

Comprehensive compensation package, which includes competitive salary, bonus, and equity for all employees
Generous paid vacation time, in addition to company-observed holidays
Excellent medical, dental, and vision insurance
401(k) retirement savings plan, which includes matching employer contributions
Employee stock purchase plan (ESPP)
Tuition reimbursement program

Fulltime

Medical Director of Revenue Integrity

The Physician Advisor is a key member of the healthcare organization’s leadershi...

Location

United States , Cheyenne

Salary:

Not provided

Cheyenne Regional Medical Center

Expiration Date

Until further notice

Requirements

Hold and maintain or able to obtain an unrestricted medical license in the state of Wyoming
Possess or acquires a solid foundation, knowledge, and/or experience in the areas of utilization management, quality improvement, and patient safety
Familiarity with InterQual and MCG is preferred
Strong understanding of Medicare Two Midnight Rules
Member of the American College of Physician Advisors (ACPA)
Board Certification by the American Board of Quality Assurance and Utilization Review Physicians, Inc. (ABQAURP) or ACPA is required within 6 months of hire
Ability to build rapport with medical staff and hospital leadership to obtain the buy-in and collaboration necessary to achieve desired outcomes
Prefer Internal Medicine specialist with a background in Hospital Medicine
Maintain active medical practice in their specialty (Can accommodate clinical time up to 0.15 FTE in the specialty (depending on availability))
Demonstrates behavior that supports the organization’s mission

Job Responsibility

Provide functional leadership for the revenue integrity team Including CDI, Coding and Utilization Review
Responsible for oversight revenue integrity optimization
Lead value-based care initiatives for the organization
Chairs the Utilization Management Team
Review medical records of patients identified by case managers or as requested by the healthcare team including physicians to perform quality and utilization oversight
Perform medical necessity reviews including initial level of care, secondary reviews, and continued stay reviews
Conduct Peer to Peer discussion with Payor Medical Directors when requested
Provide regular feedback to physicians and all other stake holders regarding level of care, length of stay, and potential quality issues
Provide necessary clinical education to UR Case Managers regarding clinical criteria and appropriate use of screening tools
Educates individual hospital staff physicians about ICD-10 and DRG coding guidelines (e.g., co-morbid conditions, outpatient vs. inpatient) and clinical terminology to improve their understanding of severity, acuity, risk of mortality, and DRG assignments on their individual patient records

What we offer

403(b) with 4% employer match
ANCC Magnet Hospital
$10,000 relocation bonus
$3,500 in CMEs
216 hours of PTO
Robust Benefits Package

Director, GxP Quality Assurance

We are establishing a dedicated GxP Quality Assurance function to support our ex...

Location

Denmark , Hørsholm

Salary:

Not provided

Life Science Talent

Expiration Date

January 12, 2026

Requirements

10+ years of GxP QA experience in biotech or pharmaceutical industry
BS or higher degree in life sciences
In-depth knowledge of global GCP regulations with a minimum of 5 years of experience in GCP QA leadership
Strong working knowledge of GMP and GLP
Experience scaling a QMS in a growing biotech is highly desired
Experience with audits and QA oversight of third-party vendors, clinical sites and internal systems and processes, either hands-on or through collaboration with external auditors or consultants
Strong understanding of computerized system validation (CSV) and data integrity principles

Job Responsibility

Lead the development and scaling of a GxP Quality Management System
Building a fit-for-purpose GxP Quality Management System: Develop and maintain a scalable QMS, govern GxP policies and SOPs, act as system owner for electronic quality systems, and drive quality metrics, management reviews and continuous improvement
Providing integrated GxP QA oversight across drug development: Lead GCP QA as Gubra enters clinical development, ensure coherent GxP governance across clinical, CMC and non-clinical programs, and drive inspection readiness in alignment with ICH E6(R3)
Managing vendors and audit programs: Oversee risk-based auditing of CROs, clinical sites, and CMC partners
Strengthen quality systems, training and culture: Improve and oversee deviation, CAPA and change control processes with robust root-cause analysis, ensuring cross-functional alignment and reporting key quality metrics

Fulltime

!

New

Director, Internal Audit

Baptist Health is hiring a Director, Internal Audit to join the Audit Services T...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Healthcare Internal Audit, Accounting, Finance or Business Degree required, Masters Degree preferred
CPA or CIA required, CFE, and CISA preferred
Strong internal control and testing experience and over five years audit leadership in the healthcare or related industry

Job Responsibility

Leading the annual and ongoing risk assessment process, developing, and managing the audit plan
Preparing and delivering regular reports to the Audit and Compliance Committee of the Board, members of the Executive Leadership and Clinical and Operational leaders
Serving as an expert resource for effective controls, best practices, and compliance
Coordinating internal audit assistance to the external auditors for the interim and annual financial audit
Leading, overseeing, and developing the internal audit team with emphasis on teamwork, innovation, efficiency, and continuous learning
Foster strong relationships with operational and clinical leaders to identify and mitigate risks and recommend opportunities to improve controls and increase efficiency

Fulltime

Clinical Auditor

Blackrock Health Hermitage Clinic

Location:
Ireland

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 03, 2026

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Clinical Auditor

Blackrock Health Hermitage Clinic

Location:Ireland

Category:Health and Beauty

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 03, 2026

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Job Posted:
January 03, 2026