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Clinical Study Administrator
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Healthcare Medical
💰 Salary Not shared
📊 Market 20,000 GBP–35,000 GBP/mo (240,000 GBP–420,000 GBP/yr)
About the Company
The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Provides solutions to a variety of issues relating to the conduct of a study of moderate scope and complexity. Typical Accountabilities: Assists in coordination and administration of clinical studies from the start-up to execution and close out. Collects, assists in preparation, reviews and tracks documents for the application process. Assists in timely submission of proper application/documents to EC/IRB and, where appropriate to Regulatory Authorities for the duration of the study. Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents. Serves as local administrative main contact and works closely with the CRAs and/or the LSAD for the duration of the study. Operational responsibility for the correct set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH-GCP and local requirements. Ensures essential documents under their responsibility are uploaded in a timely manner to maintain the eTMF "Inspection Readiness". Ensures that all study documents are ready for final archiving and completion of local par
Requirements
- ● Scientific degree that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
- ● Previous administrative experience preferably in the medical/ life science field.
- ● Proven organizational and administrative skills.
- ● Computer proficiency (Veeva Clinical Vault, SAP S/4HANA, Coupa)
- ● Good knowledge of spoken and written English.
- ● Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH-GCP guidelines.
- ● Ability to develop advanced computer skills to increase efficiency in daily tasks.
- ● Good verbal and written communication.
- ● Good interpersonal skills and ability to work in an international team environment.
- ● Willingness and ability to train others on study administration procedures.
- ● Excellent organization and time management skills, excellent attention to detail, and ability to multi-task in a high-volume environment with shifting priorities.
- ● Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
- ● Integrity and high ethical standards.
- ● Date Posted 28-sept-2026
- ● Closing Date 08-oct-2026
- ● AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Credential Requirements
for United Kingdom
🔴
Must have to work
PLAB 1 + PLAB 2
General Medical Council
Cost: GBP 1,000–2,000
Timeline: 6–18 months
🔴
Must have to work
NMC CBT + OSCE
Nursing and Midwifery Council
Cost: GBP 1,000–2,000
Timeline: 6–12 months
🔴
Must have to work
GPhC OSPAP
General Pharmaceutical Council
Cost: GBP 6,000–10,000
Timeline: 1 year
🔴
Must have to work
GDC ORE Part 1 + Part 2
General Dental Council
Cost: GBP 2,000–4,000
Timeline: 1–2 years
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