Clinical trial monitor Work, Jobs in Oxford (with Salaries)

Clinical Research Coordinator
Velocity Clinical Research, Inc. —High Wycombe
- £30,000 - £40,000 a year
- Full-time
- Nursing
- Microsoft Office
- Bachelor's degree
- Free parking
- Health & wellbeing programme
Quick apply
3d
Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
- From £58,500 a year
- English
- Microsoft Office
- Bachelor's degree
Clinical Trials Vendor Management Specialist
PSI CRO —Oxford
- Full-time
- Hybrid work
- Microsoft Office
- Business development
Quick apply
14d
Switchboard Operator
Oxford University Hospitals NHS Foundation Trust —Headington
- £25,760 - £27,476 a year
- Full-time
- University
11d
Specialist Biomedical Scientist (x2)
Deciphex —Oxford
- 8 hour shift
- Laboratory experience
- Mentoring
- Annual leave
Quick apply
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
3d
Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead
IQVIA —Reading
- English
- Microsoft Office
- Analysis skills
9h
Senior Product Manager (Pharma Clinical Trials)
Perspectum —Oxford
- £65,000 - £75,000 a year
- Full-time
- Marketing
- Presentation skills
- Bachelor's degree
Quick apply
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
15h
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —Reading
- Laboratory experience
- Project management
- Communication skills
6d
Lead Vascular Scientist
Oxford University Hospitals NHS Foundation Trust —Oxford
- £66,582 - £77,368 a year
- Full-time
- Leadership
- Communication skills
12d
Local Study Associate Director
IQVIA —Reading
- Patient monitoring
- English
- Project management
5d
Senior Biomedical Scientist
Deciphex —Oxford
- 8 hour shift
- Data analysis skills
- Laboratory experience
- English
- Flexible schedule
Quick apply
Project Manager I, IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme
5d
Senior Scientist 1
Abbott Laboratories —Witney
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
14d
Quality Engineer (Medical Devices)
Amber Therapeutics —Didcot
- Full-time
- Hybrid work
- Engineering
- Quality control
- Communication skills
Quick apply
11d
Principal Investigator
Velocity Clinical Research, Inc. —High Wycombe
- Full-time
- Travel
Quick apply
Data Standards Engineer (CDISC)
IQVIA —Reading
- Computer Science
- Java
- Bachelor's degree
6d

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Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
University degree qualified and/or comparable professional education. Act as a key point of contact for trial-related systems, documentation, and operational…
From £58,500 a year

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Clinical Research Coordinator

Velocity Clinical Research, Inc.
High Wycombe

Quick apply

Job details

Full-time
£30,000 - £40,000 a year
3 days ago

Benefits

Free parking
Health & wellbeing programme
Company pension
Employee discount
Enhanced maternity leave
Referral programme
Sick pay

Qualifications

Nursing
Clinical research
Microsoft Office
Bachelor's degree
Organisational skills
Communication skills

Full job description

Job Overview
We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulatory standards, and maintaining accurate documentation. This role offers an excellent opportunity for individuals passionate about advancing medical science and improving patient outcomes. The position is paid and suitable for candidates with a keen eye for detail, organisational skills, and a strong interest in clinical research.

Responsibilities

Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow-up.
Ensure adherence to study protocols, regulatory requirements, and ethical standards.
Collect, record, and maintain accurate trial data in accordance with Good Clinical Practice (GCP) guidelines.
Liaise with investigators, healthcare professionals, and study participants to facilitate smooth trial operations.
Monitor participant safety and report adverse events in compliance with regulatory procedures.
Prepare and submit necessary documentation to ethics committees and regulatory authorities.
Assist in training new staff or interns involved in the research projects.
Maintain organised records of all trial-related documentation for audit purposes.

Requirements

Bachelor's degree in health sciences, nursing, or a related field; relevant experience in clinical research is preferred.
Strong organisational skills with the ability to manage multiple tasks efficiently.
Excellent communication skills to liaise effectively with team members, participants, and external agencies.
Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
Ability to work independently as well as part of a multidisciplinary team.
Proficiency in data management software and Microsoft Office Suite.
Attention to detail and high level of accuracy in documentation.
Prior experience working within healthcare or research environments is advantageous but not essential. This role provides an engaging environment for professionals committed to advancing healthcare through meticulous research practices while contributing meaningfully to medical progress.

Job Type: Full-time

Pay: £30,000.00-£40,000.00 per year

Benefits:

Company pension
Employee discount
Enhanced maternity leave
Free parking
Health & wellbeing programme
Referral programme
Sick pay

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

clinical trial monitor jobs in oxford

Clinical Research Coordinator

Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)

Clinical Trials Vendor Management Specialist

Switchboard Operator

Specialist Biomedical Scientist (x2)

Clinical Trial Manager - Project Lead

Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead

Senior Product Manager (Pharma Clinical Trials)

Clinical Supplies Project Manager

Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

Lead Vascular Scientist

Local Study Associate Director

Senior Biomedical Scientist

Project Manager I, IDEA

Senior Scientist 1

Quality Engineer (Medical Devices)

Principal Investigator

Data Standards Engineer (CDISC)

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