Clinical trial manager Work, Jobs in Lower Earley, Brk (with Salaries)

Global Clinical Study Team Associate
ICON Plc —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Employee assistance programme
16h
Clinical Trials Assistant II
IQVIA —Reading
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Project Manager I
Perspectum —Oxford
- £33,000 - £45,000 a year
- Full-time
- Project management
- Communication skills
Quick apply
Dedicated Line Manager - Clinical Project Management
IQVIA —Reading
- Full-time
- Remote
- Management
- Customer service
- Microsoft Office
RWE Associate Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
4d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Clinical Data Management Lead, home-based
IQVIA —Reading
- Full-time
- Remote
- Anatomy knowledge
- Customer service
- Project management
Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
6d
Clinical Trials Manager
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Travel
- Organisational skills
- Communication skills
Project Manager, Remote Research Clinicians
IQVIA —Reading
- Full-time
- English
- Project management
- Bachelor's degree
Post-Trial Access Manager, Continued Access - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- No degree
- Employee assistance programme
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
7d
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
Project Manager
Theolytics —Oxford
- Organisational skills
- IT
- Communication skills
- Flexible schedule
Senior Product Manager (Pharma Clinical Trials)
Perspectum —Oxford
- £65,000 - £75,000 a year
- Full-time
- Marketing
- Presentation skills
- Bachelor's degree
Quick apply
Territory Manager - North West
BD —Winnersh
- £43,300 - £66,025 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Director Clinical Operations, Clinical Project Managers
IQVIA —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
14d
Project Manager - IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme

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clinical trial manager jobs near lower earley, brk

Global Clinical Study Team Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
16 hours ago

Benefits

Company pension
Employee assistance programme

Qualifications

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

Full job description

Global CTA

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Job title - Clinical Study Team Assistant

Location - Can be based in any of the following locations: UK, Spain, Italy, France, Germany and Poland

Fully sponsor dedicated

We are looking for a highly organized and proactive Clinical Study Team Assistant to join our global clinical operations team. This role plays a vital part in supporting the delivery of clinical trials, ensuring activities are executed efficiently, on time, and in line with Good Clinical Practice (GCP) and internal standards.

What You’ll Be Doing

Study Operations & Coordination

Support the Clinical Study Team Lead with day-to-day operational delivery of assigned studies
Partner with Study Managers to help coordinate site management, monitoring, and vendor activities
Manage and maintain shared study team platforms and collaboration tools

Documentation & Compliance

Oversee Trial Master File (TMF) activities, ensuring accuracy, completeness, and inspection readiness
Monitor and analyse study performance metrics, proactively following up on any gaps
Conduct quality checks on key study documentation, including regulatory and reporting materials

Systems & Data Management

Ensure study information is accurately tracked across systems and registries
Coordinate completion of study-level documentation and data entry across clinical systems
Support system setup, maintenance, and process compliance across study teams

Cross-Functional Collaboration

Work closely with global stakeholders across multiple functions and seniority levels
Provide regular updates and actively contribute to study team meetings
Support communications to study sites where required

What We’re Looking For

Qualifications & Experience

Bachelor’s degree (or equivalent) with up to 3 years’ experience, or postgraduate degree with up to 1 year’s experience
Exposure to clinical research, clinical trials, or drug development (through work or study)
Strong proficiency in Microsoft Office (Outlook, Excel, Word, PowerPoint, Teams)

Key Skills & Attributes

Excellent organization skills with the ability to manage multiple priorities simultaneously
Strong attention to detail and commitment to high-quality output
Effective communication skills—both written and verbal
Ability to work independently while contributing to a collaborative team environment
Proactive, self-motivated, and solution-oriented mindset

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

Refine Your Search

clinical trial manager jobs in lower earley, brk

Global Clinical Study Team Associate

Clinical Trials Assistant II

Clinical Project Manager I

Dedicated Line Manager - Clinical Project Management

RWE Associate Clinical Project Manager – Oncology (FSP)

Sr. Clinical Project Manager (Europe)

Clinical Data Management Lead, home-based

Regulatory and Start Up Specialist - UK

Clinical Trials Manager

Project Manager, Remote Research Clinicians

Post-Trial Access Manager, Continued Access - Sponsor Dedicated

Manager, Clinical Study Lead

Senior Quality Assurance Manager (Clinical)

Senior Clinical Trial Administrator

Senior Clinical Technology Specialist

Project Manager

Senior Product Manager (Pharma Clinical Trials)

Territory Manager - North West

Director Clinical Operations, Clinical Project Managers

Project Manager - IDEA