Junior research associate Work, Jobs in Basingstoke, Ham (with Salaries)

Clinical Research Associate
ICON Plc —Reading
- Full-time
- Nursing
- Travel
- Communication skills
- Employee assistance programme
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
14d
Associate Director - Ecology
AECOM —Basingstoke
- Full-time
- Hybrid work
IT Engineer
QinetiQ —Farnborough
- Full-time
- Engineering
- Windows
- No degree
- Employee discount
Consultant Family & Systemic Psychotherapist
Surrey and Borders Partnership NHS Foundation Trust —Frimley
- £81,774 - £93,879 a year
- Part-time
- Free parking
7d
Senior Associate - Employment
Blake Morgan —Reading
- Business development
- Analysis skills
- Communication skills
Solicitor - Special Educational Needs
Boyes Turner —Reading
- 8 hour shift
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Organisational skills
Senior Technical Actuary (GMP Equalisation)
XPS Pensions Group —Reading
- Full-time
- Hybrid work
- Microsoft Excel
- Employee discount
- Referral programme
Senior Network Engineer
QinetiQ —Farnborough
- Full-time
- Computer networking
- Employee discount

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Patient Recruitment Associate II
ICON Plc —Reading
Ability to manage multiple studies or initiatives in a fast-paced environment, with a commitment to quality and patient-centricity.
14d
Clinical Research Associate II
IQVIA —Reading
Requires at least 2 years on-site monitoring experience of interventional studies. Ensure copies/originals (as required) site documents are available for filing…

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Clinical Research Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Nursing
Clinical research
Communication skills
Nursing

Full job description

CRA II Late Phase

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.

CRA II (will consider Senior CRA) Late Phase

Home based in the UK

We are seeking a Clinical Research Associate to join ICON Commercialisation & Outcomes (ICO) — our Late Phase business. This is an exciting opportunity to work on post-marketing, real-world, and late phase studies, supporting evidence generation that demonstrates value, safety, and effectiveness in broader patient populations.

As a CRA in our Late Phase team, you will play a critical role in ensuring high-quality delivery across a mix of interventional (IP), observational and medical device studies, in various therapeutic indications, contributing to successful outcomes that shape clinical and commercial strategy.

Key Responsibilities

Site Monitoring & Oversight
Conduct on-site and remote monitoring visits across late phase studies, ensuring compliance with protocols, ICH-GCP, regulatory requirements, and applicable device regulations.
Late Phase Study Delivery
Support execution of post-authorisation, observational, and interventional studies, ensuring high-quality data collection and real-world evidence generation.
Site Performance & Issue Resolution
Evaluate site performance, identify risks, and implement solutions to ensure studies are delivered on time and to quality standards.
Cross-Functional Collaboration
Partner with project teams, medical, data management, and commercial stakeholders to ensure efficient study delivery and reporting.
Training & Mentorship
Provide guidance and support to site personnel and junior CRAs, maintaining consistency and best practice, where applicable.
Stakeholder Engagement
Build strong relationships with investigators and site staff to drive engagement and successful study execution.

Your Profile

Advanced degree in Life Sciences, Nursing, Pharmacy, or Medicine
Significant experience as a Clinical Research Associate, ideally within late phase / Phase IV / real-world studies
Experience across both investigational product (IP) and medical device trials is highly desirable
Strong understanding of ICH-GCP, regulatory requirements, and post-marketing study environments
Proven ability to manage multiple sites and competing priorities
Expertise in site monitoring, data integrity, and risk-based monitoring approaches
Proficiency in clinical systems (e.g., CTMS, EDC)
Willingness to travel across the UK to perform on-site visits
Excellent communication, stakeholder management, and influencing skills

#LI-SB2

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

junior research associate jobs in basingstoke, ham

Clinical Research Associate

Patient Recruitment Associate II

Associate Director - Ecology

IT Engineer

Consultant Family & Systemic Psychotherapist

Senior Associate - Employment

Solicitor - Special Educational Needs

Senior Technical Actuary (GMP Equalisation)

Senior Network Engineer

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