Research assistant Work, Jobs in Neath, Ntl (with Salaries)

Clinical Trials Assistant
Cyden Ltd —Swansea
- £27,000 a year
- Full-time
- Patient monitoring
- Quality control
Quick apply
Health Care Assistant/Support Worker - Wales - Our Future Health Programme
Xyla Services —Ammanford
- £19 - £26 an hour
- Part-time
- BLS Certification
- Travel
- Communication skills
Quick apply

More jobs to discover

Find similar jobs that you might be interested in.

Health Care Assistant/Support Worker - Wales - Our Future Health Programme
Xyla Services —Ammanford
Good understanding of quality standards, KPIs, risk assessment, incident reporting, and infection prevention and control. Travel: Required between local sites.
£19 - £26 an hour
Quick apply
Health Care Support Worker Clinical Skills Trainer
Cwm Taf Morgannwg University Health Board —Merthyr Tydfil
The post holder will utilise a range of teaching methods to deliver engaging, inclusive and effective education sessions, adapting their approach to meet the…
£28,819 - £31,626 a year
7d

I want to receive the latest job alerts for research assistant in neath, ntl

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

research assistant jobs near neath, ntl

Healthcare Assistant jobs in Ammanford

Clinical Assistant jobs in Sunderland

Clinical Trial Coordinator jobs in Manchester

Clinical Assistant jobs in Oxford

Rehabilitation Assistant jobs in London

Customer Assistant jobs in London

Teaching Assistant jobs in Brighton

Clinical Assistant jobs in Leeds

Clinical Assistant jobs in London

Healthcare Assistant jobs in Dartford

Healthcare Assistant jobs in Wolverhampton

Healthcare Assistant jobs in Guernsey Gy1

Uk Healthcare jobs in Remote

Healthcare Assistant jobs in Ely

Physiotherapy Assistant jobs in Birmingham

Executive Assistant jobs in Birmingham

Clinical Trials Assistant

Cyden Ltd -
Swansea

Quick apply

Job details

Permanent | Full-time
£27,000 a year

Qualifications

Healthcare research operations
Clinical research
Clinical record keeping
Patient monitoring
Patient appointment coordination
Data management
Quality control
Good Clinical Practice (GCP)
Stock replenishment
Document management
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination

Full job description

Permanent and Fixed Term positions available

Due to the nature of the role, which involves administering treatments to female participants on a one-to-one basis in a private clinical setting, and to protect participant privacy and dignity, this position is subject to a Genuine Occupational Requirement under Schedule 9 of the Equality Act 2010 for the postholder to be female.

Overall Job Purpose:

1.Support the planning, coordination, and administration of clinical trials to ensure they are conducted accurately, efficiently, and in compliance with regulatory and ethical standards. This role is essential for maintaining trial documentation, managing participant appointments, ensuring data accuracy, and upholding Good Clinical Practice (GCP) and study protocols.

2.Perform administrative and clinical tasks that facilitate the trial's progress, including data entry, documentation management, communication with participants, and coordination with clinical team members.

3.Provide valid, high-quality data that contributes to the safety and efficacy evaluations necessary for advancing products and treatments.

Key Responsibilities:

Trial Preparation: Prepare and review all study-related documents before study commencement.

Participant Recruitment: Recruit and maintain contact with trial participants throughout the study.

Scheduling: Maintain an accurate and up-to-date appointment schedule.

Informed Consent: Conduct the informed consent process with all participants.

Protocol Adherence: Execute clinical activities according to study protocols, including device treatments, photography, and skin measurements.

Data Management: Ensure complete and accurate Case Report Form (CRF) entries during trials and transcription of raw data.

Patient Monitoring: Monitor and report patient status, safety, adverse events, and device effects.

Inventory Management: Monitor clinical suite supplies and replenish as needed.

SOP Development: Assist in creating and updating Standard Operating Procedures.

Quality Control: Promptly address and report concerns arising during studies and maintain utmost confidentiality.

Key objectives/KPI's

Data accuracy and quality

Timeliness of document management

Adherence to study protocols

Patient recruitment and retention rates

Timeliness in management of participant appointments

Response time to participant queries

Monitoring and reporting Adverse Events

Inventory and supply management

Continuous improvement and training participation

Audit and inspection readiness

Skills, know-how & experience:

Ideal Experience

Experience: 1-3 years in clinical research or a related field; previous experience with clinical trial documentation or administration preferred.

Familiarity with GCP guidelines, ICH regulations, and regulatory submission processes.

Other attributes:

Problem-solving skills and the ability to anticipate needs and manage multiple priorities.

A team-oriented approach with a focus on quality, efficiency, and meeting deadlines.

Confidentiality and professionalism in handling sensitive trial information

Receptive to feedback and proactive

Self-motivated, with a can-do-attitude and the ability to work both independently and as part of a team

Quick apply

Refine Your Search

research assistant jobs in neath, ntl

Clinical Trials Assistant

Health Care Assistant/Support Worker - Wales - Our Future Health Programme

More jobs to discover

I want to receive the latest job alerts for research assistant in neath, ntl

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected