Clinical research associates & coordinators Work, Jobs in Llanelli, Wls (with Salaries)

Clinical Trials Assistant
Cyden Ltd —Swansea
- £27,000 a year
- Full-time
Quick apply
Clinical Documentation Specialist
Cyden Ltd —Swansea
- £38,000 - £42,000 a year
- Full-time
- Bachelor's degree
- Communication skills
Quick apply
3d
Project Associate
ICON Plc —Swansea
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bachelor's degree
- Organisational skills
- Employee assistance programme
2d
Site Specialist II
ICON Plc —Swansea
- Full-time
- Bachelor's degree
- Mentoring
- Business
- Employee assistance programme
8d

Other jobs to consider

Find your next job by exploring related positions.

Project Associate
ICON Plc —Swansea
Supporting financial administration, including purchase orders, invoice processing and investigator payments. During your first 3-6 months, you'll be based full…
2d
Audiology Associate Practitioner
Swansea Bay University Health Board —Swansea
The course will provide experience in assessment and interventions with routine/non-complex hearing pathologies/disabilities for patients of all ages, but with…
£28,819 - £31,626 a year
5d

I want to receive the latest job alerts for clinical research associates & coordinators in llanelli, wls

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

clinical research associates & coordinators jobs near llanelli, wls

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 research associates & coordinators jobs in llanelli, wls

Clinical Trials Assistant

Clinical Documentation Specialist

Project Associate

Site Specialist II

Other jobs to consider

I want to receive the latest job alerts for clinical research associates & coordinators in llanelli, wls

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected