Clinical trial Work, Jobs in Brighton, Esx (with Salaries)

Clinical Research Associate
IQVIA —Brighton
- Full-time
- No degree
- Travel
- Recruiting
Clinical Site Manager (Study Start Up for NPC)
Roche —Burgess Hill
- No degree
- Communication skills
10d
QA Validation Specialist
Thermo Fisher Scientific —Horsham
- Full-time
- Travel
- Communication skills
Medical Secretary / Practice PA (Private Clinic, Hurstpierpoint)
Spine and Brain LTD —Hassocks
- £25,000 - £33,000 a year
- Weekend availability
- Computer literacy
- GP surgery experience
- Administrative experience
Quick apply
3d
Client Services Associate Project Manager Packaging
Thermo Fisher Scientific —Horsham
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Computer literacy
3d
Bookkeeper / accounts and medical administrator (Private Clinic, Hurstpierpoint)
Spine and Brain LTD —Hassocks
- £25,000 - £33,000 a year
- Weekend availability
- Social media management
- Computer literacy
- GP surgery experience
Quick apply
3d
Senior Quality Compliance Specialist
Thermo Fisher Scientific —Horsham
- Full-time
- Continuous improvement
- In-person
- Communication skills
Senior Biostatistician
Theradex Oncology —Crawley
- Full-time
- Master's degree
- Communication skills
- Time management
- Employee assistance programme
- Sick pay
Client Services Project Manager Packaging
Thermo Fisher Scientific —Horsham
- Full-time
- Computer literacy
- Travel
- Organisational skills
Associate Medical Director, Cardiovascular and Renal Medical Affairs
Novo Nordisk —Gatwick Airport
- Doctoral degree
- English
- Master's degree
13d
Logistics Coordinator (12 month FTC)
Thermo Fisher Scientific —Horsham
- Full-time
- Microsoft Word
- Mentoring
- Training & development
9d
Area Business Manager - Southwest England & Wales
BD —Crawley
- £43,300 - £66,025 a year
- Weekend availability
- In-person
COA Product and Insights Manager
Wiley —Bognor Regis
- £53,000.00 - £75,866.66 a year
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
2d
Senior Manager, Operational Excellence (PPI)
Thermo Fisher Scientific —Horsham
- Full-time
- Engineering
- Bachelor's degree
- Continuous improvement
Finance Business Partner
Thermo Fisher Scientific —Horsham
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Training & development
5d

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Project Assistant - Clinical Safety
Medpace, Inc. —London
Assist with case processing activities as delegated. Contribute to an interactive team environment that empowers decision making, creative thinking, and…
4d
Assistant Psychologist/Rater - London
Re:Cognition Health —London
Perform data entry in accord with sponsor or trial requirements and systems and ensure data queries are resolved promptly. Mini-Mental State Exam (MMSE).
£31,000 - £33,000 a year
Quick apply
13d

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clinical trial jobs near brighton, esx

Clinical Research Associate

IQVIA -
Brighton

Apply Now

Job details

Full-time

Qualifications

Healthcare research operations
Clinical research
Stakeholder liaison
Filing
Recruiting
Clinical compliance monitoring
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines
Research participant recruitment coordination
Project progress tracking

Full job description

Brighton, United Kingdom | Full time | Field-based | R1514135

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK

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 Good Clinical Practice.
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 of Oncology therapeutic area for unblinded studies.
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 as required

*Please note - this role is not eligible for 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

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

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 trial jobs in brighton, esx

Clinical Research Associate

Clinical Site Manager (Study Start Up for NPC)

QA Validation Specialist

Medical Secretary / Practice PA (Private Clinic, Hurstpierpoint)

Client Services Associate Project Manager Packaging

Bookkeeper / accounts and medical administrator (Private Clinic, Hurstpierpoint)

Senior Quality Compliance Specialist

Senior Biostatistician

Client Services Project Manager Packaging

Associate Medical Director, Cardiovascular and Renal Medical Affairs

Logistics Coordinator (12 month FTC)

Area Business Manager - Southwest England & Wales

COA Product and Insights Manager

Senior Manager, Operational Excellence (PPI)

Finance Business Partner

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