Clinical research Work, Jobs in Frimley, Sry (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
5d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
8d
Head of Virology (ID4520)
Animal and Plant Health Agency —New Haw
- £73,165 - £81,535 a year
- Overtime
- Doctoral degree
- Presentation skills
- Leadership
- Annual leave
- Employee discount
8d
Senior Pharmacovigilance Officer
Milpharm Ltd —Uxbridge
- £28,000 - £35,000 a year
- Full-time
- Nursing
- English
- Bachelor's degree
- Life insurance
- Sick pay
Quick apply
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
5d
Cardiovascular Clinical Research Fellow
Buckinghamshire Healthcare NHS Trust —High Wycombe
- £67,325 - £76,582 a year
- Full-time
- Annual leave
1d
Director, Statistical Programming
CSL Behring —Maidenhead
- £239,000 - £308,000 a year
- Full-time
- Computer Science
- Maintenance
- English
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
9d
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
6d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- No degree
- Travel
1d
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
- Project management
- Bachelor's degree
- Continuous improvement
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Patient-Centered Outcomes Research (PCOR) Lead (UK)
UCB —Slough
- Doctoral degree
- Master's degree
- Leadership
2d
Director, Global Clinical Physician, Late Hematology, Oncology, and Cell Therapy (HOCT)
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Patient monitoring
- Travel
- In-person
Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)
ICR —London
- £66,092 - £86,908 a year
- Doctoral degree
- Master's degree
Medical Advisor, Neuropsychiatry
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Project management
- Travel
- In-person
Health Economic Expert (UK posting)
UCB —Slough
- Doctoral degree
- Master's degree
- Analysis skills
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
12d

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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
5 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 research jobs in frimley, sry

Clinical Research Coordinator

Clinical Research Scientist

Head of Virology (ID4520)

Senior Pharmacovigilance Officer

Study Start Up Associate

Cardiovascular Clinical Research Fellow

Director, Statistical Programming

Clinical Trial Associate

Research Facilitator

Clinical Research Associate - IQVIA Biotech

Manager, Clinical Study Lead

Sr. Clinical Project Manager (Europe)

RWE Senior/ Clinical Project Manager (FSP)

Senior Clinical Programmer I

Patient-Centered Outcomes Research (PCOR) Lead (UK)

Director, Global Clinical Physician, Late Hematology, Oncology, and Cell Therapy (HOCT)

Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)

Medical Advisor, Neuropsychiatry

Health Economic Expert (UK posting)

CRA

I want to receive the latest job alerts for clinical research in frimley, sry

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