Clinical research associates & coordinators Work, Jobs in Hook, Ham (with Salaries)

Clinical Research Trainee
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
10h
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
4d
Senior Clinical Project Support Specialist - Sponsor dedicated (m/w/d)
IQVIA —Reading
- From £58,500 a year
- English
- Microsoft Office
- Bachelor's degree
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
7d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
6d
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
4d
Clinical Trial Program Lead
Eli Lilly —Bracknell
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Associate Clinical Project Manager (UK)
UCB —Slough
- English
- Bachelor's degree
6d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
10d
Sr. CRA 1 - Site Management
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Study Start Up Associate
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
6d
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
3d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Data Manager -B4
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Full-time
- Administrative experience
- IT
- Medical terminology
4d
Site Start-Up Specialist
Fortrea —Maidenhead
- Full-time
- Hybrid work
- Microsoft Office
- Communication skills
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Unblinded CRA I
Fortrea —Maidenhead
- Full-time
- Nursing
- English
- Travel
4d
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
17h

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clinical research associates & coordinators jobs near hook, ham

Clinical Research Trainee

IQVIA -
Reading

Apply Now

Job details

Temp to perm | Full-time | Fixed term contract | Internship
10 hours ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Clinical research
Bachelor's degree
Communication skills

Full job description

Kickstart Your Career in Clinical Research with IQVIA!

Are you passionate about clinical research and eager to start your journey?

As a clinical intern with our site management (multi-sponsor) team, you will assist clinical trials whilst receiving comprehensive training through our development program.

We are offering a full time and paid trainee role on a 9-month fixed term contract, with the potential to become permanent upon completion.

Job Overview

Assist with accurately updating and maintaining clinical documents and systems (e.g.,Trial Master File (TMF)) that track site compliance and performance within project timelines
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures
Assist with periodic review of study files for completeness
Assist the Country Site Activation team with preparation, handling and

distribution of Clinical Trial Supplies and maintenance of tracking information

Complete CSA training program and develop knowledge of clinical research, Good Clinical Practice (GCP) and appropriate therapeutic area and protocols
Accompany CSAs on site visits to assist with clinical monitoring duties upon completion of required training

What We’re Looking For

Bachelor’s degree in a scientific or healthcare discipline
Passion for clinical research and ambition to grow into a CRA role
Proficiency in Microsoft Word, Excel, and PowerPoint
Strong communication skills and ability to build effective relationships

*This position is not eligible for UK visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical research associates & coordinators jobs in hook, ham

Clinical Research Trainee

Study Start Up Associate

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

Clinical Trial Associate

Clinical Research Scientist

Research Facilitator

Clinical Trial Program Lead

Sr. Clinical Project Manager (Europe)

Associate Clinical Project Manager (UK)

CRA 2 - Single Sponsor Dedicated

CRA

Sr. CRA 1 - Site Management

Senior Study Start Up Associate

Clinical Trial Manager - Project Lead

Senior Clinical Programmer I

Data Manager -B4

Site Start-Up Specialist

Sr. CRA 1 - Single Sponsor Dedicated

Unblinded CRA I

Clinical Supplies Project Manager

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