Clinical research Work, Jobs in Frimley, Sry (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
9d
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
4d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
7d
Head of Virology (ID4520)
Animal and Plant Health Agency —New Haw
- £73,165 - £81,535 a year
- Overtime
- Doctoral degree
- Presentation skills
- Leadership
- Annual leave
- Employee discount
8d
Senior Pharmacovigilance Officer
Milpharm Ltd —Uxbridge
- £28,000 - £35,000 a year
- Full-time
- Nursing
- English
- Bachelor's degree
- Life insurance
- Sick pay
Quick apply
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
5d
Cardiovascular Clinical Research Fellow
Buckinghamshire Healthcare NHS Trust —High Wycombe
- £67,325 - £76,582 a year
- Full-time
- Annual leave
22h
Director, Statistical Programming
CSL Behring —Maidenhead
- £239,000 - £308,000 a year
- Full-time
- Computer Science
- Maintenance
- English
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
5d
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
- Project management
- Bachelor's degree
- Continuous improvement
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- No degree
- Travel
1d
Assoc Director, Clinical Operations
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Master's degree
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Patient-Centered Outcomes Research (PCOR) Lead (UK)
UCB —Slough
- Doctoral degree
- Master's degree
- Leadership
2d
Director, Global Clinical Physician, Late Hematology, Oncology, and Cell Therapy (HOCT)
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Patient monitoring
- Travel
- In-person
Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)
ICR —London
- £66,092 - £86,908 a year
- Doctoral degree
- Master's degree
Medical Advisor, Neuropsychiatry
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Project management
- Travel
- In-person
Health Economic Expert (UK posting)
UCB —Slough
- Doctoral degree
- Master's degree
- Analysis skills

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clinical research jobs near frimley, sry

Clinical Trial Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
9 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Bachelor's degree
Organisational skills

Full job description

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 - CTA (relevant experience required)

Location - Must be within a commutable distance to London (2 days office presence required)

Fully sponsor dedicated

As a Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do:

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key responsibilities include:

Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile:

You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
Willingness to travel as required (approximately 10%)

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 .

Are you a current ICON Employee?

Apply Now

Refine Your Search

clinical research jobs in frimley, sry

Clinical Trial Associate

Clinical Research Coordinator

Clinical Research Scientist

Head of Virology (ID4520)

Senior Pharmacovigilance Officer

Study Start Up Associate

Cardiovascular Clinical Research Fellow

Director, Statistical Programming

Research Facilitator

Manager, Clinical Study Lead

Sr. Clinical Project Manager (Europe)

RWE Senior/ Clinical Project Manager (FSP)

Clinical Research Associate - IQVIA Biotech

Assoc Director, Clinical Operations

Senior Clinical Programmer I

Patient-Centered Outcomes Research (PCOR) Lead (UK)

Director, Global Clinical Physician, Late Hematology, Oncology, and Cell Therapy (HOCT)

Research Group Leader, ICR Clinical Trials and Statistics Unit (ICR-CTSU)

Medical Advisor, Neuropsychiatry

Health Economic Expert (UK posting)

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