Research assistant Work, Jobs in Bletchley, Bkm (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
6d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills

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Clinical Trial Administrator
University of Oxford —Oxford
The successful candidate will support a wide range of trial activities, including organising meetings, taking minutes, managing trial documentation, responding…
£32,108 a year
2d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
Support internal audits and regulatory inspections as needed including providing requested regulatory documents and all other inspection activities as required.

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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
6 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

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