Clinical trial administrator Work, Jobs in Stanton Harcourt, Oxf (with Salaries)

Study Administrative Assistant/ Data Coordinator
University of Oxford —Oxford
- £32,108 a year
- Full-time
- Microsoft Office
- Administrative experience
- Data entry
9d
Clinical Research Trials Assistant
University of Oxford —Oxford
- £32,108 - £37,338 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Doctoral degree
- Annual leave
6d
Clinical Research Administator
University of Oxford —Oxford
- £32,108 - £40,514 a year
- Full-time
- Oracle
- Administrative experience
- Organisational skills
Clinical Trials Administrator with Play
University of Oxford —Oxford
- £28,437 - £34,732 a year
- Full-time
- Administrative experience
- In-person
- Communication skills
5d
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- Project management
- Annual leave
9d
Senior Trial Administrator- Haematology Trials Unit
Oxford University Hospitals NHS Foundation Trust —Oxford
- £39,959 - £48,117 a year
- Full-time
20h

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Clinical Research Trials Assistant
University of Oxford —Oxford
This post is full-time and fixed term for 2 years. Membership to a variety of social and sports clubs. As a member of the research team your role will involve a…
£32,108 - £37,338 a year
6d
Research Assistant
University of Oxford —Oxford
You will hold an undergraduate degree in Biological Science, together with relevant laboratory experience, including handling human blood samples and performing…
£35,681 - £41,636 a year

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Study Administrative Assistant/ Data Coordinator

University of Oxford -
Oxford

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Job details

Full-time | Fixed term contract
£32,108 a year
9 days ago

Qualifications

Relational databases
Microsoft Office
Administrative experience
Data management
Data entry
Organisational skills
IT

Full job description

The Nuffield Department of Women's & Reproductive Health (NDWRH) is seeking a Study Administrative Assistant/ Data Coordinator to jointhe global maternal health research team supporting the E-MASTER research programme.

E-MASTER is an international programme of research aiming to improve the early detection and treatment of postpartum haemorrhage during caesarean birth, with the ultimate goal of improving maternal outcomes worldwide.

Working closely with the Chief Investigator, International Coordinator, Programme Manager, Programme Officer and Clinical Study Administrators, the postholder will play a key role in ensuring the smooth day-to-day running of this multi-country clinical study. They will provide high-quality administrative and data management support, helping to maintain robust study systems, ensuring data integrity and contributing to the efficient delivery of this important global health research programme.

The role offers a varied range of responsibilities including organising meetings, preparing agendas and taking minutes, responding to participant and site enquiries, maintaining study documentation, supporting participant follow-up, managing study supplies and assisting with study promotion and recruitment activities. The postholder will also be responsible for supporting data collection, data cleaning, validation and reconciliation, implementing quality control procedures, resolving data queries and ensuring study documentation is maintained and archived in accordance with study procedures.

The post will involve working closely with colleagues across the study team and with recruiting sites to develop effective working relationships that support high-quality study delivery. The post also offers opportunities to contribute to the continuous improvement of administrative and data management processes and to support study reporting and oversight activities.

Applicants should have experience of managing administrative processes together with experience of data entry and working with large databases. Strong organisational skills, excellent attention to detail, and the ability to prioritise competing workloads while meeting deadlines are essential. Candidates should also possess excellent IT skills, including experience using Microsoft Office applications and relational databases or similar systems, together with an understanding of confidentiality, GDPR and good data management principles.

Experience of working within clinical trials, healthcare research or using REDCap is desirable but not essential.

The post is offered on a full-time basis (part-time considered) and is fixed term until 30 June 2027 in the first instance. Applications for flexible working arrangements are welcomed and will be considered in line with business needs.

You will be required to upload a CV and Supporting Statement as part of your online application. Click here for information and advice on writing an effective Supporting Statement.

The closing date for applications is 12.00 noon on Monday 3rd August. Interviews for this post are expected to take place mid-late August.

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clinical trial administrator jobs in stanton harcourt, oxf

Study Administrative Assistant/ Data Coordinator

Clinical Research Trials Assistant

Clinical Research Administator

Clinical Trials Administrator with Play

Trial Manager

Senior Trial Administrator- Haematology Trials Unit

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