Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks
Support system compliance and system data entry, as applicable
File required task-related documentation in the Electronic Trial Master File (eTMF)
Review initial/amended Country/Site ICFs in compliance with Sponsor requirements, local regulatory requirements and Good Clinical Practice (GCP) guidelines.
Liaising and follow-up with local teams, Start-up Project Managers, and Sponsors to assure timely approval of Informed Consent Forms in order to meet submission deadlines.
To follow all applicable departmental Standard Operating Procedures and Work Instructions:
To complete required trainings according to required timelines.
To complete day-to-day tasks ensuring quality and productivity.
To manage project and technical documentation in an appropriate manner.
To provide administrative and technical support to internal departments and teams as needed.
To perform checks to ensure quality of work completed.
To ensure timely escalation and issue resolution as needed.
To participate in process improvement opportunities and assist with the implementation of revised processes and procedures.
All other duties as needed or assigned.
Qualifications (Minimum Required):
University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)
Fortrea may consider relevant and equivalent experience in lieu of educational requirements
Experience (Minimum Required):
Working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines.
3-5 years' work experience in clinical research
Previous interaction with operational project teams preferred.
Preferred Qualifications Include:
Computer proficiency in MS Office (Word, Excel, PowerPoint, Access, Outlook e-mail and internet services)
Good written and oral communication skills
Well-developed organizational skills
Excellent proof-reading skills
Physical Demands/Work Environment:
General Office Environment.
Learn more about our EEO & Accommodations request here.
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Frequently Asked Questions
Everything you need to know about finding your next role
How does Global Work AI apply to jobs without spamming?
Global Work AI only applies to roles that closely match your experience, seniority, and career goals. Each application is personalized and submitted intentionally-one role at a time-so it looks human, relevant, and never spammy.
Is Global Work AI safe for my professional reputation?
Yes. Protecting your professional reputation is built into the product. We avoid mass applications, irrelevant roles, and generic language. Every application is tailored to the role and designed to reflect how a strong candidate would apply manually.
Do I need a “perfect” resume to use Global Work AI?
No. You don’t need a perfect resume to get started. Global Work AI uses your existing resume to build a Candidate Profile, then adapts your resume for each role-highlighting what matters most.
What will my resume and cover letter look like before they’re submitted?
You stay fully in control. Before anything is submitted, you can review how your resume and cover letter are tailored for the role-clear, focused, and aligned with the job description.
Will recruiters be able to tell that I used AI to apply?
No. Applications are designed to look natural and intentional. Because each one is role-specific and personalized, they don’t resemble the generic or automated submissions that recruiters are accustomed to filtering out.
What if I’m not satisfied with Global Work AI?
We want you to feel confident trying Global Work AI. If you’re not satisfied, you can rely on our Money-Back Guarantee. Contact our support team at contact@globalwork.ai , and we’ll assist you.