Clinical data coordinator Work, Jobs in Wooburn, Bkm (with Salaries)

Clinical Research Assistant
Velocity Clinical Research, Inc. —High Wycombe
- Temporary
- Data entry
- Medical terminology
- Communication skills
2d
Patient Care Coordinator in Luxury Private Hospital
Berkshire Grove Hospital —Maidenhead
- £14 - £16 an hour
- Full-time
- Administrative experience
- Data entry
- Organisational skills
- Free parking
Quick apply
Clinical Trials Coordinator - London
Re:Cognition Health —London
- £34,000 - £38,000 a year
- Microsoft Powerpoint
- Microsoft Word
- Business development
- Annual leave
- Employee assistance programme
Quick apply
7d
Research Coordinator - Patient Services
Anthony Nolan —London
- £34,000 a year
- Hybrid work
- No degree
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
7d
Senior Clinical Data Coordinator - FSP (Homebased - UK)
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
13d
Clinical Research Coordinator I
Velocity Clinical Research, Inc. —London
- Temporary
- Computer literacy
- Writing skills
- English
1d
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Clinical Discharge Coordinator
Buckinghamshire Healthcare NHS Trust —Aylesbury
- £39,959 - £48,117 a year
- Part-time
- Discharge planning
- Organisational skills
- Communication skills
- Annual leave
2d
Clinical Data Manager - FSP (Homebased - UK)
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
13d
Cancer MDT Coordinator
Chelsea and Westminster Hospital NHS Foundation Trust —London
- £36,943 - £44,900 a year
- Part-time
- Data entry
- Organisational skills
- Communication skills
8d
Sustainability Coordinator
Medik8 —Aylesbury
- £30,000 - £32,000 a year
- Monday to Friday
- Hybrid work
- Training & development
- Leadership
- Employee discount
Quick apply
2h
Beneficiary Services Project Co-ordinator
Police Care UK —Woking
- £29,120 a year
- Full-time
- CRM software
- Organisational skills
- Annual leave
1d
UKDTN Community Engagement Coordinator
University College London —London
- £36,433 - £42,891 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- Organisational skills
- Annual leave
- Employee assistance programme
11d
Patient Services Co-ordinator (GP Receptionist/Administraton) Self-Employed Contractor
St John's Way Medical Centre —London
- £525 a week
- Temporary
- Computer literacy
- GP surgery experience
- Administrative experience
Quick apply
2d
Operational Support Services & Systems Receptionist
Kingston and Richmond NHS Foundation Trust —Teddington
- £29,651 - £31,312 a year
- Part-time
- Remote
- Microsoft Word
- Microsoft Outlook
- Writing skills
- Annual leave
- Employee assistance programme
3d
CRC Associate
ICON Plc —North London
- Full-time
- Vital signs
- Organisational skills
- Communication skills
- Employee assistance programme
Elective Care Telephonist - Part Time
Harrow Health CIC —Rickmansworth
- £12.71 an hour
- Part-time
- Administrative experience
- In-person
- Office experience
Quick apply
MDT / Patient Pathway Coordinator
Royal National Orthopaedic Hospital NHS Trust —Stanmore
- £33,262 - £36,027 a year
- Full-time
- Communication skills
1d
Patient Coordinator - London
Re:Cognition Health —London
- £32,000 - £35,000 a year
- Bilingual
- Annual leave
- Employee assistance programme
Quick apply
2d
Medical Director - Oncology , Sponsor Dedicated (Home-Based)
IQVIA —Reading
- Full-time
- Remote
- Management
- Sales
- Business development
- Work from home
14d

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Clinical Research Assistant

Velocity Clinical Research, Inc. -
High Wycombe

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:

Required Skills and Abilities
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 duties and responsibilities described above are intended to describe the general nature and level of work performed in this position. They are not an exhaustive list of all duties, responsibilities, or qualifications required. Duties may change based on business and operational requirements.

Apply Now

Refine Your Search

clinical data coordinator jobs in wooburn, bkm

Clinical Research Assistant

Patient Care Coordinator in Luxury Private Hospital

Clinical Trials Coordinator - London

Research Coordinator - Patient Services

Senior Clinical Data Coordinator - FSP (Homebased - UK)

Clinical Research Coordinator I

Senior Clinical Data Manager - sponsor dedicated - oncology

Clinical Discharge Coordinator

Clinical Data Manager - FSP (Homebased - UK)

Cancer MDT Coordinator

Sustainability Coordinator

Beneficiary Services Project Co-ordinator

UKDTN Community Engagement Coordinator

Patient Services Co-ordinator (GP Receptionist/Administraton) Self-Employed Contractor

Operational Support Services & Systems Receptionist

CRC Associate

Elective Care Telephonist - Part Time

MDT / Patient Pathway Coordinator

Patient Coordinator - London

Medical Director - Oncology , Sponsor Dedicated (Home-Based)

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