Clinical specialist Work, Jobs in Llandow, Vgl (with Salaries)

Clinical Documentation Specialist
Cyden Ltd —Swansea
- £38,000 - £42,000 a year
- Full-time
- Bachelor's degree
- Communication skills
Quick apply
5h
Rehabilitation Specialist
Nuffield Health —Vale of Glamorgan
- Up to £27,985 a year
- Full-time
- English
- Bachelor's degree
- Rehabilitation centre
- Employee discount
- Gym membership
Trainee Clinical Scientist- Genomics (route 2)
Cardiff and Vale University Health Board —Whitchurch
- £40,559 - £48,841 a year
- Full-time
- English
- Bachelor's degree
3d
Skin Cancer Screening Nurse
The MOLE Clinic Ltd —Cardiff
- Up to £42,000 a year
- Full-time
- No experience needed
- In-person
- Nursing
- Annual leave
- Employee discount
Quick apply
13d
Cardiff Metropolitan University MH Mentors and ASC & SpLD Study Skills Tutors
Amano Technologies Ltd —Cardiff
- £34.02 an hour
- Hybrid work
- Master's degree
- University
- Mentoring
Quick apply
Clinical Assessor
Capita Health Assessment Advisory Service —Cardiff
- £39,500 a year
- Full-time
- Hybrid work
- Microsoft Office
- Analysis skills
- IT
- Paid training
- Employee discount
Quick apply
Clinical Support Nurse
South Wales Police —Coychurch
- £33,603 - £39,276 a year
- Weekend availability
- Nursing
- Annual leave
- Employee assistance programme
7d
Head of People
Cwm Taf Morgannwg University Health Board —Abercynon
- £67,583 - £78,530 a year
- Full-time
- Hybrid work
- Recruiting
- Leadership
- Analytics
10d
Site Specialist II
ICON Plc —Swansea
- Full-time
- Bachelor's degree
- Mentoring
- Business
- Employee assistance programme
6d
NHS Wales - Trainee Clinical Scientist - Radiotherapy Physics
Swansea Bay University Health Board —Swansea
- £40,559 - £48,841 a year
- Full-time
- English
3d
Functional Specialist - Clinic Based - Cardiff
Capita Health Assessment Advisory Service —Cardiff
- £39,500 a year
- Full-time
- Microsoft Office
- IT
- Communication skills
- Employee discount
- Referral programme
Quick apply
Specialist Podiatrist
Swansea Bay University Health Board —Bridgend
- £40,559 - £48,841 a year
- Full-time
- Hospital
- English
3d
Technician Demonstrator (Sports Rehabilitation and Massage)
Cardiff Metropolitan University —Cardiff
- £39,906 - £44,746 a year
- Part-time
- Administrative experience
- Rehabilitation centre
- IT
- Annual leave
Specialist Addictions Nurse
Aneurin Bevan University Health Board —Caerphilly
- £40,559 - £48,841 a year
- Part-time
- Case management
- Negotiation
- Nursing
- Paid training
9d
Research and Insight Manager
Moondance Cancer Initiative —Cardiff
- £42,000 a year
- Full-time
- Hybrid work
- Analysis skills
- No degree
- Communication skills
- Annual leave
Quick apply
6d
Pharmaceutical Production Operator
Cardiff and Vale University Health Board —Cardiff
- £26,813 - £27,890 a year
- Full-time
- Inventory control
- Quality control
- Organisational skills
1h
Mental Health & Learning Disabilities Care Group Medical Director
Cwm Taf Morgannwg University Health Board —Bridgend
- £114,099 - £166,585 a year
- Part-time
- English
- Leadership
Head of Workforce Productivity, Value & Effectiveness
Cwm Taf Morgannwg University Health Board —Abercynon
- £80,698 - £92,984 a year
- Full-time
- Hybrid work
2d
Clinical Nurse Specialist
Velindre Cancer Centre —Cardiff
- £40,559 - £48,841 a year
- Part-time
- Patient care
- Communication skills
12d
Consultant Ophthalmologist - Medical Retina (Regional)
Swansea Bay University Health Board —Swansea
- £114,099 - £166,585 a year
- Full-time
- English
4d

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Clinical Documentation Specialist

Cyden Ltd -
Swansea

Quick apply

Job details

Full-time
£38,000 - £42,000 a year
5 hours ago

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 specialist jobs in llandow, vgl

Clinical Documentation Specialist

Rehabilitation Specialist

Trainee Clinical Scientist- Genomics (route 2)

Skin Cancer Screening Nurse

Cardiff Metropolitan University MH Mentors and ASC & SpLD Study Skills Tutors

Clinical Assessor

Clinical Support Nurse

Head of People

Site Specialist II

NHS Wales - Trainee Clinical Scientist - Radiotherapy Physics

Functional Specialist - Clinic Based - Cardiff

Specialist Podiatrist

Technician Demonstrator (Sports Rehabilitation and Massage)

Specialist Addictions Nurse

Research and Insight Manager

Pharmaceutical Production Operator

Mental Health & Learning Disabilities Care Group Medical Director

Head of Workforce Productivity, Value & Effectiveness

Clinical Nurse Specialist

Consultant Ophthalmologist - Medical Retina (Regional)

I want to receive the latest job alerts for clinical specialist in llandow, vgl

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