Study Specialist II - Global Study Operations
CTM3072024_1719910441
Posted: 07/02/2024
- £340 - £380 PER DAY
- City of London, London
- Contract
Job Title: Study Specialist II - Global Study Operations
Work location: Holborn, Central London
Contract duration: Initial 6-months (Inside IR35)
Work schedule: Monday - Friday. Minimum of 2 days in the central London office (Wednesday + 1 other), with up to 3 days from home.
Pay rate: £340 - £380/day
About the Role:
Are you passionate about advancing therapies for rare and life-threatening genetic diseases? We are seeking a dedicated Study Specialist II to join a leading bio-pharmaceuticals Global Study Operations team, contributing to this mission of delivering meaningful therapeutic advances to patients worldwide.
As a Study Specialist II - Global Study Operations you will play a vital role in overseeing site monitoring, site management, and vendor management. You will support various study-related activities impacting time-lines, quality, and budget. Your expertise will contribute to the successful execution of clinical studies, ensuring high-quality data to support regulatory approvals.
Key Responsibilities for the Study Specialist II - Global Study Operations may include:
- Develop and review study-specific documentation.
- Manage country and site feasibility assessments.
- Support regulatory document collection and tracking.
- Oversee essential document management.
- Develop training materials for sites and investigators.
- Manage investigator payments and site setups.
- Provide administrative support for internal and external meetings.
- Identify and mitigate risks.
- Support vendor management.
- Maintain essential documents in the Trial Master File (TMF).
Qualifications & Experience:
- BS or higher in nursing, life sciences, or health sciences preferred. Relevant industry experience may be considered.
- Experience overseeing external vendors (e.g., CROs, central labs).
- Experience in Phase 1-3 trials is essential.
- Experience in rare diseases and/or gene therapy is highly desired.
Join our client and contribute to groundbreaking work that makes a real difference in patients' lives. Apply today to be part of an innovative and dynamic environment!
Please note: You must be able to work in the UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: +44 (0)20 7551 0727 (UK) / +31 208 089 982 (NL)
Jada Kirlew
Senior Candidate Consultant I
