Research and development Work, Jobs in Port Talbot, Wls (with Salaries)

Clinical Trials Assistant
Cyden Ltd —Swansea
- £27,000 a year
- Full-time
- Patient monitoring
- Quality control
Quick apply
Project Coordinator
SANS Institute —Swansea
- Full-time
- Hybrid work
- Management
- Writing skills
- Research
Quick apply
10d
Legal Assistant - Residential New Build Property
HCB Widdows Mason —Swansea
- Microsoft Word
- Organisational skills
- Communication skills
Quick apply
In-house SEO Content Writer
PHSGroup —Caerphilly
- Monday to Friday
- Hybrid work
- In-person
- Free parking
- Annual leave
In-house SEO Content Writer
PHS Group —Caerphilly
- Full-time
- Hybrid work
- In-person
- Free parking
- Annual leave
Adviser (trainee roles considered)
Citizens Advice Caerphilly Blaenau Gwent —Bargoed
- £25,597 - £27,034 a year
- Hybrid work
- Communication skills
- Annual leave
- Employee assistance programme
12d
PBS practitioner
ivolve Care and Support —Bridgend
- £26,812.50 - £29,152.50 a year
- Full-time
- Research
- Travel
- Training & development
- Annual leave
- Referral programme
Service Delivery Lead - Wales - Our Future Health Programme
Xyla Services —Neath
- £31 - £40 an hour
- Part-time
- Customer service
- BLS Certification
- Continuous improvement
Quick apply
Associate Director of Public Health (NWJCC)
Cwm Taf Morgannwg University Health Board —Pontypridd
- £114,475 - £131,732 a year
- Full-time
- Leadership
- Annual leave
12d
Antenatal Clerical Officer/Receptionist
Aneurin Bevan University Health Board —Ystrad Mynach
- £26,300 a year
- Part-time
- Data entry
- Front desk
- Communication skills
10d
Research and Development Specialist
RAM Innovations —Pentre
- Full-time
- Analysis skills
- Continuous improvement
- In-person
- Annual leave
Communications Apprentice
Hafod —Cardiff
- £12.71 an hour
- Full-time
- Travel
Contract Manager - National Energy Projects
Knights Brown —Bridgend
- Business development
- Continuous improvement
- Team management
4037 - Director of Data & Assurance for the Disused Tips Authority
Welsh Government —Merthyr Tydfil
- £82,089 - £99,500 a year
- Full-time
- Presentation skills
- Leadership
- Communication skills
Service Delivery Lead
SANS Institute —Swansea
- Full-time
- Hybrid work
- Management
- Computer literacy
- Writing skills
Quick apply
10d
Data Compliance and Systems Audit Officer
South Wales Police —Bridgend
- £27,204 - £32,613 a year
- Full-time
- Analysis skills
- Annual leave
3d
Cash Desk Volunteer
British Heart Foundation —Port Talbot
- Cash handling
- Employee discount
Stockroom Volunteer
British Heart Foundation —Port Talbot
- Employee discount
Product Developer
Sigma 3 Kitchens —Pontyclun
- £28,000 - £31,000 a year
- Full-time
- Data analysis skills
- Analysis skills
- Bachelor's degree
- Employee assistance programme
- Employee discount
Quick apply
10d
Associate Director, Workforce Transformation Psychological Professions
Health Education and Improvement Wales —Cardiff
- £80,698 - £92,984 a year
- Part-time
- Research
- Training & development
9d

I want to receive the latest job alerts for research and development in port talbot, wls

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

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 and development jobs in port talbot, wls

Clinical Trials Assistant

Project Coordinator

Legal Assistant - Residential New Build Property

In-house SEO Content Writer

In-house SEO Content Writer

Adviser (trainee roles considered)

PBS practitioner

Service Delivery Lead - Wales - Our Future Health Programme

Associate Director of Public Health (NWJCC)

Antenatal Clerical Officer/Receptionist

Research and Development Specialist

Communications Apprentice

Contract Manager - National Energy Projects

4037 - Director of Data & Assurance for the Disused Tips Authority

Service Delivery Lead

Data Compliance and Systems Audit Officer

Cash Desk Volunteer

Stockroom Volunteer

Product Developer

Associate Director, Workforce Transformation Psychological Professions

I want to receive the latest job alerts for research and development in port talbot, wls

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected