Clinical research associate Work, Jobs in Mortimer Common, Ham (with Salaries)

Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Employee assistance programme
12h
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
12d
Clinical Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
8d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
12d
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d
Study Start Up Associate II
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Travel
- Employee assistance programme
7d
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
14d
Manager - Patient Experience Data
IQVIA —Reading
- Full-time
- Remote
- Project management
- IT
- Time management
2d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Payment Specialist
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Contracts
- In-person
- Annual leave
- Employee assistance programme
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
2d
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £250,000 - £280,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
2d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Sr CRA - Oncology experienced required
ICON Plc —Reading
- Full-time
- Programmable logic controllers
- Travel
- Communication skills
- Employee assistance programme
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- Negotiation
Director Biostatistics
CSL Behring —Maidenhead
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Travel
2d

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Clinical Research Associate
ICON Plc —Reading
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.

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clinical research associate jobs near mortimer common, ham

Clinical Research Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Driving Licence
Clinical research
Bachelor's degree
Organisational skills
Communication skills

Full job description

Clinical Research Associate - Single Sponsor - 3/4 SIV's per month

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.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

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 research associate jobs in mortimer common, ham

Clinical Research Associate

Clinical Research Associate II

Clinical Trial Associate

Clinical Research Associate - 12 months' monitoring experience required

Clinical Contracts Associate

Senior Clinical Research Associate

Research Facilitator

Senior Clinical Trial Associate

Study Start Up Associate II

Patient Recruitment Associate II

Manager - Patient Experience Data

CRA

Payment Specialist

Senior CRA

Director, Portfolio Development Process & Standards Lead

Specialist, R&D Contracts & Business Operations

Sr CRA - Oncology experienced required

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Director Biostatistics

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