Clinical documentation specialist Work, Jobs in Wls (with Salaries)

Clinical Documentation Specialist
Cyden Ltd —Swansea
- £38,000 - £42,000 a year
- Full-time
- Bachelor's degree
- Communication skills
Quick apply
Multi-Disciplinary Team (MDT) Co-ordinator - Cancer Services
Hywel Dda University Health Board —Carmarthen
- £28,819 - £31,626 a year
- Full-time
- Organisational skills
1d
Site Specialist II
ICON Plc —Swansea
- Full-time
- Bachelor's degree
- Mentoring
- Business
- Employee assistance programme
Waste, Medical Devices & Health and Safety Compliance Lead
Spire Healthcare —Wrexham
- £26,122 a year
- Full-time
- Microsoft Word
- Hospital
- Communication skills
- Free parking
- Annual leave
11d
Community Heart Failure Clinical Nurse Specialist
Hywel Dda University Health Board —Milford Haven
- £40,559 - £48,841 a year
- Part-time
- Organisational skills
- Communication skills
- Nursing
9d
Inquest Team Manager
Cwm Taf Morgannwg University Health Board —Abercynon
- £50,129 - £57,365 a year
- Full-time
- Analysis skills
- Organisational skills
- Training & development
Business Development Manager (Northwest and North Wales)
Hydrafacial —Bangor
- £42,000 - £48,500 a year
- Marketing
- Salesforce
- Business development
Quick apply
Principal Scientist - Immunoassay & Clinical Biomarkers
Simbec-Orion —Merthyr Tydfil
- Full-time
- Management
- Doctoral degree
- Master's degree
Mental Capacity Act and Consent Practitioner
Cwm Taf Morgannwg University Health Board —Abercynon
- £50,129 - £57,365 a year
- Full-time
- Communication skills
2d
Clinical Research Specialist Nurse - Immunology
Cardiff and Vale University Health Board —Cardiff
- £40,559 - £48,841 a year
- Full-time
7d
Bank Highly Specialist Cardiac Physiologist (Echocardiology)
Powys Teaching Health Board —Brecon
- £46,840 - £53,602 a year
- Part-time
- Inventory control
- Research
- Patient care
Clinical Research Nurse
Cardiff and Vale University Health Board —Cardiff
- £32,557 - £39,631 a year
- Part-time
7d
Engineer
Spire Healthcare —Wrexham
- £30,900 a year
- Full-time
- In-person
- Free parking
- Annual leave
Principal Scientist - Small Molecule LC-MS/MS
Simbec-Orion —Merthyr Tydfil
- Full-time
- Doctoral degree
- Master's degree
- Team management
6d
Outpatient Nurse (Pain Management)
SJK Healthcare Limited —Haverfordwest
- £24 - £25 an hour
- Part-time
- Communication skills
- Nursing
Quick apply
Outpatient Nurse (Respiratory)
SJK Healthcare Limited —Aberystwyth
- £24 - £25 an hour
- Part-time
- Acute care experience
- Communication skills
Quick apply
Costs Lawyer/Draftsman - Personal Injury
Redkite Solicitors —Cardiff
- Full-time
- Travel
- Communication skills
- Annual leave
Senior Specialist Speech & Language Therapist
Brainkind —Pontyates
- £49,387 a year
- Part-time
- Discharge planning
- Free parking
- Employee assistance programme
Quick apply
Consultant in Oral Medicine
Cardiff and Vale University Health Board —Cardiff
- £114,099 - £166,585 a year
- Full-time
- Teaching
Consultant in Oral & Maxillofacial Surgery
Cardiff and Vale University Health Board —Cardiff
- £114,099 - £166,585 a year
- Full-time
- Management
- Surgery
- Mentoring

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Clinical Documentation Specialist

Cyden Ltd -
Swansea

Quick apply

Job details

Full-time
£38,000 - £42,000 a year

Qualifications

Document control
Clinical research
Stakeholder collaboration
Compliance audits
Bachelor's degree
Clinical audit participation
Clinical compliance monitoring
Technical writing
Document control software
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Proofreading
Document management
Document management systems
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
FDA regulations

Full job description

FIXED TERM OPPORTUNITY- 5 MONTHS

Overall job purpose

Maintain and develop the clinical department documentation framework, defining templates, work instructions (WIs) and procedures at sponsor level and site level.
Update and create work instructions (WIs), standard operating procedures (SOPs), and templates for clinical operations in alignment with evolving regulations (FDA, ISO 14155, EU MDR, etc.).
Ensure version control, document history tracking, and archival procedures are correctly applied.
Act as document control delegate for all clinical documentation, ensuring timely release for use and accurate version tracking.
Collaborate with Medical Writers, Biostatistician, CRA, CTA manager and CTA's within the clinical team to ensure documentation reflects current best practice, ease of usability and compliance to both regulations and clinical investigation plans.
Manage and maintain Case Report Forms Templates (CRFs), create CRF completion guidelines and associated clinical documentation at a study level.
Monitor changes in regulations and standards that may impact clinical documentation requirements and ensure framework remains compliant.
Conduct document reviews, audits, and gap analyses to identify compliance risks.

Key Responsibilities:

CRF & Data Collection Documentation

Collaborate with Medical Writer, Clinical Biostatistician and CRA to design CRFs, eCRFs and logs that align with study protocols and regulatory requirements.

Work closely with CTA's to create and amend documentation templates and SOPs that minimize data entry errors and reflect best practice.

Draft and maintain CRF Completion Guidelines (CCGs) for investigator sites.

Ensure CRF updates are tracked, version-controlled, and integrated into EDC platforms.

Collaborate clinical trials software engineer and with Support user acceptance testing (UAT) of EDC CRFs and system configuration.

o Translate CRF into EDC format

o Develop UAT scripts for system testing

o Participate in and document UAT activities

o Validated EDC system

o Signed UAT logs

o Audit trail documentation

Clinical Documentation Standards

Ensure documentation aligns with ISO 14155 for medical device clinical investigations and applicable ICH-GCP guidelines.

Support in ethical approval processes by ensuring all applicable templates and documentation meet ethical standards and comply with any ethical committee requirements.

Develop and maintain standardized clinical document templates (protocols, monitoring plans, ICFs, etc.) that are appliable for use across multiple study applications.

Develop and maintain work instructions, SOPs and procedures for use across the clinical department.

Complete annual gap analysis of the existing documentation at both a sponsor and site level, where gaps are identified create clear processes, timelines and supporting WIs/templates for implementation.

Review and update existing clinical SOPs, WIs, and procedural documentation annually in alignment with:

o ICH-GCP E6 (R3)

o ISO 14155:2020 (Clinical Investigation of Medical Devices)

o FDA 21 CFR Part 812, Part 11

o EU MDR documentation standards

Document Control & Quality Oversight

Ensure controlled documents are appropriately authored, reviewed, approved, and archived per company document management SOPs.

Maintain traceability logs, version control logs, change histories, and audit trails for all documentation.

Act as document control delegate for all clinical documentation, ensuring timely release for use and accurate version tracking.

Assist in preparation for audits, inspections, and internal quality reviews.

Cross-Functional Collaboration & Support

Act as a subject matter expert (SME) on clinical documentation practices for internal teams.

Support training and onboarding of new clinical staff regarding document standards and CRF completion guidelines.

Work closely with Medical Writers to identify and create any documentation required to execute clinical investigation plans on an individual study basis.

Provide study specific training sessions to CTAs and other site level staff to outline all documentation required, provide overview of any new study specific templates and data collection timepoints.

Work closely with CRA and CTA Manager to resolve documentation discrepancies and ensure compliance and consistency at investigational sites.

Experience/ Skills:

Essential

3+ years of experience in clinical research, with direct involvement in CRF design, WI/SOP writing and clinical documentation control.

Experience working on medical device trials, especially pre-market (feasibility, pivotal) studies.

Ability to interpret regulatory guidance into SOPs/WIs.

Strong technical writing, proofreading, and document formatting skills.

Meticulous attention to detail.

Detail-oriented with excellent organizational and version control capabilities.

Proficient in document management systems (eTMF systems) and Microsoft Office Suite.

Familiarity with EDC platforms.

Knowledge of clinical operations processes.

Cross-functional communication skills.

Desirable

Experience supporting aesthetic, dermatologic, or medical device studies at both sponsor and site level.

Understanding of data collection best practices, coding systems (MedDRA,) and risk-based monitoring.

Ability to work independently while managing multiple projects in a fast-paced environment.

Collaborative mindset with a commitment to cross-functional excellence and process improvement.

Education/ Qualifications/ Training:

Essential

Bachelor's degree in Life Sciences, Health Sciences, Biomedical Engineering, or a related field.

Proven deep knowledge of clinical documentation and applying regulatory frameworks (FDA, ISO, GCP, MDR)

Deep knowledge of GCP (ICH E6 R3), ISO 14155 (device trials), 21 CFR Part 11 (electronic records), 21 CFR Part 812 (device IDE studies) and the ability to translate this regulations to practical documents.

FDA & EMA guidance on clinical documentation

Familiarity of good documentation practices (GDP)

Quick apply

Refine Your Search

clinical documentation specialist jobs in wls

Clinical Documentation Specialist

Multi-Disciplinary Team (MDT) Co-ordinator - Cancer Services

Site Specialist II

Waste, Medical Devices & Health and Safety Compliance Lead

Community Heart Failure Clinical Nurse Specialist

Inquest Team Manager

Business Development Manager (Northwest and North Wales)

Principal Scientist - Immunoassay & Clinical Biomarkers

Mental Capacity Act and Consent Practitioner

Clinical Research Specialist Nurse - Immunology

Bank Highly Specialist Cardiac Physiologist (Echocardiology)

Clinical Research Nurse

Engineer

Principal Scientist - Small Molecule LC-MS/MS

Outpatient Nurse (Pain Management)

Outpatient Nurse (Respiratory)

Costs Lawyer/Draftsman - Personal Injury

Senior Specialist Speech & Language Therapist

Consultant in Oral Medicine

Consultant in Oral & Maxillofacial Surgery

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