Study Specialist I (Global Study Operations)

JR United Kingdom; London; Hybrid; GBP 30,000 - 45,000; Full time

Job summary

A leading company in clinical operations is seeking a Study Specialist I in London. The successful candidate will provide essential administrative support to clinical study teams, managing documentation and coordinating activities within a dynamic research environment. Ideal for candidates with strong organizational skills and a proactive attitude, this role requires expertise in Microsoft Office and an interest in global clinical study operations.

Qualifications

• Experience in clinical research or healthcare preferred.
• Strong attention to detail and organizational skills required.
• Proficiency in Microsoft Office Suite (Excel, Word, Outlook) needed.

Responsibilities

• Support document management tasks related to eTMF, SharePoint, and Teams.
• Track clinical trial insurance processes and monitor expiration dates.
• Assist with internal and external meetings and teleconferences.

Skills

Attention to Detail

Organizational Skills

Collaborative Attitude

Proactive Approach

Education

Administrative or Operations Experience

Tools

Microsoft Office Suite

Zoom

Microsoft Teams

SharePoint

Job description

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Study Specialist I (Global Study Operations), london

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Client:

i-Pharm Consulting

Location:

london, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

24.06.2025

Expiry Date:

08.08.2025

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Job Description:

Job Title: Study Specialist I (Global Study Operations)

Period - 12 Month Contract (Extension Possible)

Location - United Kingdom, London (Hybrid - 2 Days On Site)

Desirable: Experience With Rare Diseases

The Study Specialist I supports clinical study operations by providing administrative and logistical support to study teams and department members. This role is not assigned to a specific study or program but instead contributes flexibly across projects as needed. The individual will assist with document management, departmental coordination, compliance tracking, and cross-functional communications, ensuring operational efficiency within the clinical development environment.

This role is ideal for candidates with strong administrative experience, attention to detail, and an interest in contributing to global clinical study operations.

Key Responsibilities:

• Maintain and update program rosters and departmental compliance metrics (e.g., BOARD Quarterly MVR).
• Manage and maintain departmental websites and document repositories (Teams, SharePoint).
• Serve as Knowledge Manager, overseeing reconciliation and filing between internal platforms.
• Support document management tasks related to eTMF, SharePoint, and Teams (uploading, correcting, reviewing, reporting).
• Assist in coordinating internal and external meetings and teleconferences.
• Process documents requiring DocuSign signatures, including IP package reviews and informed consent forms.
• Track and support clinical trial insurance processes, including monitoring expiration dates, renewals, certificate distribution, and archiving.
• Facilitate mass communications and department-wide email/mail distributions.
• Provide ad-hoc or short-term support to study teams when requested and approved.

Requirements:

• Administrative or operations experience in a professional setting, preferably within clinical research or healthcare.
• Strong attention to detail and organizational skills.
• Collaborative, proactive attitude with the ability to prioritize and manage multiple tasks.
• Proficiency in Microsoft Office Suite (Excel, Word, Outlook), Zoom, and Microsoft Teams.
• Experience with document management platforms such as SharePoint is a plus.
• Familiarity with clinical study documentation and terminology is helpful but not required.

If you are interested in finding out more about this role or others, please contact Sharleney Chandraratna at [emailprotected] or call: [phone]