Clinical assistant Work, Jobs in Llanelli, Cmn (with Salaries)

Clinical Trials Assistant
Cyden Ltd —Swansea
- £27,000 a year
- Full-time
Quick apply
Tritech & Innovation Research Assistant
Hywel Dda University Health Board —Llanelli
- £28,819 - £31,626 a year
- Full-time
- English
- Microsoft Office
- Organisational skills
10d
Retail Assistant (Opticians)
Boots —Carmarthenshire
- Weekend availability
- Employee assistance programme
- Employee discount
Healthcare Assistant
Circle Health Group —Carmarthen
- £24,947 a year
- Part-time
- Hospital
- IT
- Communication skills
- Employee discount
- Life insurance
13d
Trainee or Qualified Pharmacy Assistant
Well Pharmacy —Swansea
- £12.71 an hour
- Employee discount
Rapid Response Care Assistant
Advantage Healthcare Limited —Swansea
- Up to £19 an hour
- Day shift
- Travel
- Annual leave
- Referral programme
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
8d
Trainee Pharmacy Assistant
Well Pharmacy —Neath
- £12.24 an hour
- Employee discount
7d
Care Assistant
Advantage Healthcare Limited —Swansea
- £15 an hour
- Weekend availability
- No experience needed
- Travel
- Paid training
- Employee discount
7d
Dental Nurse / Trainee dental NUrse
gupta dental durgeons —Port Talbot
- £12.71 - £14.50 an hour
- Part-time
- CAD
- Bachelor's degree
- Computer skills
- Free parking
- Employee discount
Quick apply
Pharmacist
Well Pharmacy —Llandeilo
- £26 an hour
- Management
- Employee discount
Support Worker
Active Care Group —Carmarthen
- £12.75 - £14.00 an hour
- 12 hour shift
- Travel
- Annual leave
- Referral programme
Quick apply
12d

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Tritech & Innovation Research Assistant
Hywel Dda University Health Board —Llanelli
Key responsibilities include coordinating meetings, workshops and project activities; maintaining study documentation and filing systems; arranging clinic…
£28,819 - £31,626 a year
10d

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clinical assistant jobs near llanelli, cmn

Clinical Trials Assistant

Cyden Ltd -
Swansea

Quick apply

Job details

Permanent | Full-time
£27,000 a year

Qualifications

Clinical research

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

clinical assistant jobs in llanelli, cmn

Clinical Trials Assistant

Tritech & Innovation Research Assistant

Retail Assistant (Opticians)

Healthcare Assistant

Trainee or Qualified Pharmacy Assistant

Rapid Response Care Assistant

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

Trainee Pharmacy Assistant

Care Assistant

Dental Nurse / Trainee dental NUrse

Pharmacist

Support Worker

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