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

Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
5d
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
7d
Clinical Trial Assistant
IWT PHU Single Corporate Service —Portsmouth
- £25,760 - £27,476 a year
- Weekend availability
- Vital signs
- Computer literacy
- Microsoft Office
Quick apply
8d
Clinical Trial Program Lead
Eli Lilly —Bracknell
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Nurse
University Hospital Southampton NHS Foundation Trust —Southampton
- £32,073 - £39,043 a year
- Full-time
- IT
- Communication skills
- Time management
11d
Data Quality Coordinator/Personal Assistant
University Hospital Southampton NHS Foundation Trust —Southampton
- £28,392 - £31,157 a year
- Full-time
- Administrative experience
- Organisational skills
- IT
5d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- No degree
- Travel
7h
RWE Senior/ Clinical Project Manager (FSP)
IQVIA —Reading
- Project management
- Bachelor's degree
- Continuous improvement
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
CRA 2 - Single Sponsor Dedicated
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
7d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
11d
Sr. CRA 1 - Site Management
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
4d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Specialist Research Nurse
IWT PHU Single Corporate Service —Portsmouth
- £39,959 - £48,117 a year
- Full-time
- No experience needed
- Supervising experience
- Project management
Quick apply
11d
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
1d
Local Study Associate Director
IQVIA —Reading
- Patient monitoring
- English
- Project management
6d

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clinical research associates & coordinators jobs near dummer, ham

Study Start Up Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
5 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Bachelor's degree
Organisational skills
Communication skills

Full job description

Study Start Up - Trial Maintenance

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.

As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
Maintaining accurate and up-to-date records of regulatory submissions and approvals.
Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
Participating in study start-up meetings and providing input on regulatory requirements and timelines.

Your Profile:

You will bring relevant site start-up and activation experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in life sciences or a related field.
Previous experience in clinical research or regulatory affairs preferred, but Nt required.
Strong attention to detail and organizational skills.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
Willingness to travel as required (approximately 5%)

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 associates & coordinators jobs in dummer, ham

Study Start Up Associate

Clinical Trial Associate

Clinical Research Scientist

Clinical Trial Assistant

Clinical Trial Program Lead

Research Nurse

Data Quality Coordinator/Personal Assistant

Clinical Research Associate - IQVIA Biotech

RWE Senior/ Clinical Project Manager (FSP)

Sr. Clinical Project Manager (Europe)

CRA 2 - Single Sponsor Dedicated

Senior Study Start Up Associate

CRA

Sr. CRA 1 - Site Management

Clinical Trial Manager - Project Lead

Senior Clinical Programmer I

Sr. CRA 1 - Single Sponsor Dedicated

Specialist Research Nurse

Clinical Supplies Project Manager

Local Study Associate Director

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