Medical Research Administrator jobs in Edinburgh
- ICON PlcLivingston
- Employee assistance programme
- Company pension
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- ICON is a global healthcare intelligence and clinical research…
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- Public Library of ScienceEdinburgh
- Company pension
- Paid volunteer time
- Private medical insurance
- Experience in a research or clinical environment, publishing, or other relevant setting; experience in medical publishing strongly preferred.
- RoslinCT EUEdinburgh EH16 4UX
- Annual leave
- Employee discount
- Company pension
- Private medical insurance
- Cycle to work scheme
- Due to the nature and training requirements of this role, applicants must have the legal right to work in the UK with sufficient permission to meet the needs of…
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- University of EdinburghEdinburgh
- Annual leave
- Employee discount
- Company pension
- The postholder will coordinate and deliver clinical research activities at the Glasgow site for the Scotland-wide multiple sclerosis (MS) research study,…
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- University of EdinburghEdinburgh
- Annual leave
- Employee discount
- Company pension
- School of Neurological and Cardiovascular Sciences / Centre for Clinical Brain Sciences.
- Full-time: 35 hours per week.
- View all University of Edinburgh jobs - Edinburgh jobs
- Salary Search: Postdoctoral Research Fellow salaries in Edinburgh
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- University of EdinburghEdinburgh
- Annual leave
- Employee discount
- Company pension
- School of Neurological and Cardiovascular Sciences / Centre for Clinical Brain Sciences.
- Full-time: 35 hours per week.
- View all University of Edinburgh jobs - Edinburgh jobs
- Salary Search: Postdoctoral Research Fellow salaries in Edinburgh
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- University of EdinburghEdinburgh
- Annual leave
- Employee discount
- Company pension
- Full-time: 35 hours per week.
- We are also open to considering requests for hybrid working (on a non-contractual basis) that combines a mix of remote and regular…
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- NHS ScotlandEdinburgh EH16 4SA
- You will play a key role in shaping research governance practices, supporting inspection readiness, and driving quality improvement across a dynamic research…
- NHS ScotlandEdinburgh EH4 2XU
- To provide effective, efficient support and administration service to the Colorectal Cancer Coordinating Team and to support service delivery on an ongoing…
- IQVIALivingston
- Work from home
- Minimum of 3 years’ experience managing data in support of clinical research.
- Experience working in highly diverse teams within clinical research; cross-…
Job Post Details
CRA 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.
As a CRA II 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 clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- 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:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
- 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.
- Willingness to travel as required (approximately 60%)
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?