Clinical associate Work, Jobs in Hermitage, Brk (with Salaries)

CRA2 - Multi-Sponsor Department
IQVIA —Reading
- Full-time
- Remote
- No degree
- Work from home
Clinical Research Associate I
PSI CRO —Oxford
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
Quick apply
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
12d
Executive Assistant with Business Development Support
PsychWorks Associates Ltd —Reading
- Up to £30,000 a year
- Part-time
- Microsoft Excel
- Sales
- Social media management
- Annual leave
Quick apply
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Experienced CRA - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- No degree
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Data analysis skills
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Doctoral degree
- Data analysis skills
- Annual leave
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d
Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
3d
Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Medical Writer - 6 Month Fixed Term Contract
BD —Winnersh
- £43,300 - £66,025 a year
- English
- Master's degree
- Presentation skills
Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Communication skills
- Annual leave
Nursing Associate
Dr Howells & Partners —Hungerford
- Up to £29,095 a year
- Full-time
- Driving
- Computer skills
- In-person
- Free parking
- Employee discount
Quick apply
Senior Research Associate, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Annual leave
Associate Case Manager
Active Care Group —Oxford
- £50 - £60 an hour
- Case management
- Travel
- Organisational skills
Quick apply
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
11d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
10d

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CRA2 - Multi-Sponsor Department

IQVIA -
Reading

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Project implementation

Full job description

Reading, United Kingdom | Full time | Home-based | R1530767

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate

Requirements

Experience of independent on-site monitoring
You have successfully managed multiple clinical trial protocols across diverse investigative sites.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites

Please note - this role 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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical associate jobs in hermitage, brk

CRA2 - Multi-Sponsor Department

Clinical Research Associate I

Clinical Trial Associate

Executive Assistant with Business Development Support

Clinical Research Associate II

Experienced CRA - Single Sponsor Dedicated

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

CRA 2 - Single Sponsor Dedicated

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

Sr. CRA 1 - Single Sponsor Dedicated

Study Start Up Associate

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

Medical Writer - 6 Month Fixed Term Contract

Senior Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

Nursing Associate

Senior Research Associate, Bioanalytical & Molecular Assays

Associate Case Manager

Associate Director Global CMC QU – Clinical GMP/GDP

Local Study Associate Director

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