Clinical trial Work, Jobs in Slough, Brk (with Salaries)

Safety Scientist
ICON Plc —Reading
- Full-time
- Analysis skills
- Bachelor's degree
- Communication skills
- Employee assistance programme
Clinical Trial Assistant – Observational Studies
Oracle —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Life insurance
Clinical Research Physician
ICON Plc —Reading
- Full-time
- Hybrid work
- Travel
- Communication skills
- Employee assistance programme
9d
Clinical Trials Assistant
London School of Hygiene & Tropical Medicine —London
- £30,231 - £33,925 a year
- Full-time
- Bachelor's degree
- Annual leave
4d
Clinical Trials Assistant II
IQVIA —Reading
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Research Associate II
IQVIA —Reading
- No degree
Research Assistant - Bank
hVIVO Services Limited —London
- Weekend availability
- Laboratory experience
- Communication skills
Director, Business Development
ICON Plc —Reading
- Full-time
- Public speaking
- Business development
- Analysis skills
- Employee assistance programme
Research Assistant
University College London —London
- £39,148 - £41,833 a year
- Full-time
- Hybrid work
- Data analysis skills
- Bachelor's degree
- Organisational skills
- Annual leave
- Employee assistance programme
7d
Trial Manager
University College London —London
- £44,480 a year
- Part-time
- Hybrid work
- Doctoral degree
- University
- Annual leave
- Employee assistance programme
10d
Clinical Trial Manager
Precision for Medicine —London
- Remote
- Microsoft Powerpoint
- Management
- English
Quick apply
Medical Secretary/PA
Dementech Limited —London
- From £30,000 a year
- Full-time
- English
- Microsoft Office
- Administrative experience
Quick apply
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Clinical Trial Manager
Precision Medicine Group —London
- Remote
- Microsoft Powerpoint
- Management
- English
Medical Doctor (UK) - Freelance AI Trainer Project
Meridial —London
- £40 - £120 an hour
- Remote
- AI
- Annual leave
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
9d
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Microsoft Excel
- English
- Annual leave
9d
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
AI Clinical Product Researcher
Odin Vision —London
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- Travel

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Safety Scientist

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Analysis skills
Bachelor's degree
Communication skills

Full job description

Safety Scientist - Remote based in UK, Poland, Bulgaria, Ireland, or Spain

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 Safety Scientist at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

Conducting safety surveillance activities for assigned projects, including the review and interpretation of safety data.
Partnership with cross-functional teams to ensure the safety of study participants and compliance with regulatory requirements.
Contributing to the development and implementation of safety management plans and risk minimization strategies.
Participating in safety review meetings and providing expert input on safety-related matters.
Contributing to the preparation of safety-related documents for regulatory submissions and responses to regulatory queries.

Your Profile:

You will bring relevant scientific operations experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Minimum of 2 years of experience in pharmacovigilance or drug safety within the pharmaceutical or clinical research industry.
Strong understanding of pharmacovigilance principles, regulations, and guidelines.
Excellent analytical and critical thinking skills, with the ability to interpret complex medical data.
Effective communication skills, with the ability to cooperate effectively with cross-functional teams.
Detail-oriented and able to work effectively in a fast-paced environment with changing priorities.

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 jobs in slough, brk

Safety Scientist

Clinical Trial Assistant – Observational Studies

Clinical Research Physician

Clinical Trials Assistant

Clinical Trials Assistant II

Clinical Research Associate II

Research Assistant - Bank

Director, Business Development

Research Assistant

Trial Manager

Clinical Trial Manager

Medical Secretary/PA

Clinical Trial Associate Manager

Clinical Trial Manager

Medical Doctor (UK) - Freelance AI Trainer Project

eClinical Coordinator (London)

Clinical Research Associate

eClinical Coordinator (London, Entry Level)

Clinical Evaluation Specialist

AI Clinical Product Researcher

I want to receive the latest job alerts for clinical trial in slough, brk

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