Biomedical Science jobs in Scotland
- ICON PlcLivingston
- Employee assistance programme
- Company pension
- Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Life assurance and disability coverage.
- View all ICON Plc jobs - Livingston jobs - Clinical Data Coordinator jobs in Livingston
- Salary Search: Clinical Data Coordinator II salaries in Livingston
- See popular questions & answers about ICON Plc
- University of StrathclydeGlasgow
- Ocan and Marine Engineering (NAOME) is recognised nationally and internationally for its excellence in teaching and.
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- University of StrathclydeGlasgow
- FTE: 1 (35 hours/week).
- By collaborating with internal teams, external partners, and patients, the CDMA chapter provides crucial medical insights, designs and executes clinical studies…
- By collaborating with internal teams, external partners, and patients, the CDMA chapter provides crucial medical insights, designs and executes clinical studies…
- Heriot Watt UniversityEdinburgh
- Annual leave
- Role: Research Associate in Bioengineering - Design, material sourcing, fabrication and implementation of a Microelectrode array scanning system for cardiac…
- University of DundeeDundee
- There will be opportunities to gain experience in areas such as project management, data science and analytics and information governance.
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- University of DundeeDundee
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- University of AberdeenAberdeen AB24
- A talented and creative researcher is sought to take part in a highly interdisciplinary project funded by the European Research Council (ERC).
- University of AberdeenAberdeen AB24
- It’s mission is to support better long-term decision-making in health and social care (see REAL Supply).
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- University of AberdeenAberdeen AB24
- It’s mission is to support better long-term decision-making in health and social care (see REAL Supply).
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- AliveDxPenicuik EH26 0BF
- Annual leave
- Additional leave
- Cycle to work scheme
- The role is a full-time permanent position working 37.5 hours per week.
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- Terumo AorticInchinnan PA4
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- Ferring Pharmaceuticals, Inc.East Kilbride
- As Global QA Senior Manager, Medical Devices & Drug/Device Combined Products, you will lead Major Global QA Medical Device projects, and you will support the…
- RoukenBioMotherwell ML1 3ST
- Referral programme
- Company pension
- On-site parking
- As Senior Study Manager you will be a specialist in the management of projects within a specific scientific subject area.
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Job Post Details
Clinical Data Coordinator II - job post
Job details
Job type
- Full-time
Location
Benefits
Pulled from the full job description
- Employee assistance programme
- Company pension
Full job description
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’re looking for a Clinical Data Coordinator II to join our growing team in Livingston, UK. This is a fantastic opportunity for recent graduates and early-career professionals who want to build hands-on experience in clinical research while working alongside experienced specialists in a collaborative, office-based environment.
At ICON plc, you’ll help support the design and analysis of clinical trials, work with real-world medical data, and develop valuable skills that contribute to the development of innovative new treatments. With strong mentorship and learning opportunities, this role offers an excellent starting point for building a career in the clinical research industry.
What you will be doing
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Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
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Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
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Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
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Address data related questions and recommend potential solutions.
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Identify root cause to systematically resolve data issues.
Your profile
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Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
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Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
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Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
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Strong attention to detail and the ability to work effectively in a fast-paced environment.
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Excellent communication skills and the ability to collaborate with cross-functional teams.
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Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
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.