Scientific goods in Work, Jobs in Rainham, Gtl (with Salaries)

Clinical Research Assistant
Velocity Clinical Research, Inc. —London
- Temporary
- Data entry
- Medical terminology
- Communication skills
2d
Support Technician Agilent Measurement Suite
Imperial College London —White City
- £42,505 - £47,213 a year
- Full-time
- Computer literacy
- Annual leave
Assistant Healthcare Scientist
UK Health Security Agency —Colindale
- £29,613 - £30,266 a year
- Part-time
- Computer literacy
- Laboratory experience
- Presentation skills
9d
QA Executive
Crescent Pharma —Park Royal
- £30,000 - £35,000 a year
- Full-time
- Microsoft Office
- Continuous improvement
- Quality control
- Free parking
- Life insurance
Quick apply
8d
Production Chemist
Siemens Healthineers —London
- Weekend availability
- Communication skills
Freelance Medical Content Writer
Doctify —London
- Remote
- English
- Research
- Data entry
Sterile Services Technician I
Steris —London
- £25,272 a year
- Overtime
- Computer literacy
- No experience needed
- Assembly
- Annual leave
10d
Internship Opportunities with Quantinuum 2026 - UK/Germany
Quantinuum —London
- Master's degree
- Internship
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Master's degree
- Business development
- Psychology
- Annual leave
- Gym membership
Associate QC Analyst
Sekisui Diagnostics —Maidstone
- Analysis skills
- Quality control
Quick apply
Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)
Imperial College London —White City
- £59,808 - £71,793 a year
- Full-time
- Bachelor's degree
- Training & development
- Annual leave
11d
Computer Support Officer (Help Desk)
Imperial College London —South Kensington
- £42,505 - £47,213 a year
- Full-time
- Communication skills
- Annual leave
2d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
Research Associate
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Research
- Organisational skills
Clinical Safety Coordinator
Medpace, Inc. —London
- Full-time
- Microsoft Office
- Bachelor's degree
- In-person
- Annual leave
- Work from home
Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation
Pharmaron —Hoddesdon
- Master's degree
- Bachelor's degree
- Mentoring
Senior Scientist, R&D
Basecamp Research —London
- Full-time
- Mentoring
- Life insurance
Quick apply
7d
Quality Lab Manager
Tropic Skincare —Croydon
- £45,000 - £50,000 a year
- Monday to Friday
- Hybrid work
- Engineering
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
Lab Engineer
Diffractive Labs —London
- Full-time
- Laboratory experience
- Maintenance
- Scripting
Quality Test Engineer III
Elsevier —London
- Full-time
- Java
- Employee assistance programme
- Employee discount

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Clinical Research Assistant

Velocity Clinical Research, Inc. -
London

Apply Now

Job details

Temporary
2 days ago

Qualifications

Clinical research
Phlebotomy
UK GDPR
Microsoft Office Suite
General Data Protection Regulation (GDPR)
Data entry
Laboratory consumables stocking
Venepuncture
NVQ
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Stock replenishment
Medical terminology
BTEC
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
A Level
Research participant recruitment coordination
Time management

Full job description

Overview:

Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.

As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.

Summary:

The Clinical Research Assistant supports the Clinical Operations Team in the conduct of clinical research studies by performing clinical, laboratory, administrative, and data management activities. The role assists with the collection, documentation, and maintenance of clinical trial data while ensuring compliance with study protocols, UK Good Clinical Practice (GCP), Medicines and Healthcare products Regulatory Agency (MHRA) requirements, and Company Standard Operating Procedures (SOPs).

Responsibilities:

Duties/Responsibilities:

Assist in the conduct of clinical trials in accordance with study protocols, UK GCP, ICH-GCP guidelines, MHRA requirements, and Company SOPs.
Perform venepuncture, capillary blood collection, and other protocol-required specimen collection procedures within the scope of training, competency, and applicable requirements.
Support clinical assessments, including vital signs, electrocardiograms (ECGs), phlebotomy, and other protocol-specific procedures under appropriate supervision.
Process, package, and ship laboratory specimens in accordance with protocol requirements, IATA regulations, and applicable UK requirements.
Maintain laboratory, study, and clinical supplies, including inventory tracking and replenishment.
Enter source data into sponsor and/or vendor electronic systems and assist in resolving basic data queries under the guidance of the Clinical Research Coordinator.
Ensure accurate, complete, and timely documentation in accordance with Good Documentation Practice standards.
Communicate effectively with participants, colleagues, investigators, sponsors, Contract Research Organisations (CROs), and vendors.
Support informed consent discussions and processes, ensuring participant understanding and ongoing consent in accordance with GCP requirements.
Assist with the preparation, maintenance, and filing of essential study documentation and regulatory records.
Support participant recruitment and retention activities, including pre-screening potential participants by telephone or in person.
Maintain strict confidentiality of participant, sponsor, and Company information in accordance with UK GDPR and the Data Protection Act 2018.
Escalate participant safety concerns, adverse events (AEs), serious adverse events (SAEs), and other protocol-defined safety issues promptly to the Clinical Research Team.
Maintain clean, organised, and compliant clinical and laboratory environments.
Prepare source documentation and file study-related documents and medical records as required.
Provide administrative support, including answering telephone calls, scheduling participant visits, issuing reminders, and maintaining participant tracking systems.
Perform other duties as assigned.

Qualifications:

Education/Experience:

Essential
- GCSEs (or equivalent) in English and Mathematics.
- Previous experience in healthcare, clinical research, laboratory sciences, or a related life sciences environment.
Desirable
- Level 3 qualification, such as A-Level, BTEC, NVQ, or equivalent, in a life sciences, healthcare, or scientific discipline.
- Previous experience within a clinical research setting.
- Knowledge of GCP principles.

Required Skills:

Basic knowledge of medical terminology.
Strong verbal and written communication skills.
Good organisational and time-management abilities.
Ability to work effectively within a multidisciplinary team.
Ability to follow written procedures and regulatory requirements.
Proficiency in Microsoft Office applications and standard office technology.
Strong attention to detail and commitment to data accuracy.
Ability to manage multiple priorities in a fast-paced environment.
Flexibility and adaptability to changing study and site requirements.
Commitment to participant safety, confidentiality, and quality standards.

NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.

Apply Now

Refine Your Search

scientific goods in jobs in rainham, gtl

Clinical Research Assistant

Support Technician Agilent Measurement Suite

Assistant Healthcare Scientist

QA Executive

Production Chemist

Freelance Medical Content Writer

Sterile Services Technician I

Internship Opportunities with Quantinuum 2026 - UK/Germany

Associate (Clinical Outcome Assessments - COA)

Associate QC Analyst

Portfolio Manager, Imperial Clinical Trials Unit (Maternity Cover)

Computer Support Officer (Help Desk)

Research Regulatory Facilitator

Research Associate

Clinical Safety Coordinator

Scientist / Associate Principal Scientist – Discovery Bioanalysis & Biotransformation

Senior Scientist, R&D

Quality Lab Manager

Lab Engineer

Quality Test Engineer III

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