Global Clinical Trial Operation - Emerging Talent Rotation Associate - Remote

Job Posting

Under the oversight of the line-manager, mentor, or rotational assignment manager, this position involves a 24-36 month committed experience rotating throughout Research and Development Division / Global Clinical Trial Operations in various clinical trial functions in preparation for movement into next roles. This role will collaborate throughout Global Clinical Trial Operations local, country, and HQ levels, with trial management, data management, country operations, and other areas. This role will rotate through various organizations, teams, and functions within Research and Development Division and Global Clinical Trial Operations to gain broad clinical research exposure and experience in support of clinical trial execution. The role assists in meeting Site Ready objectives, IRB / ERC and Health Authorities submissions, study execution objectives, data management responsibilities, clinical / non-clinical supply management, and ensures timely maintenance of tracking and reporting tools, as applicable, in support of clinical trial delivery.

Responsibilities may include, but are not limited to :

• Trial and site administration and management :
• Track essential documents and report issues as applicable
• Ensure collation and distribution of study tools and documents
• Update clinical trial databases (CTMS) and trackers
• Clinical supply & non-clinical supply management, in collaboration with other country roles
• Manage Labeling requirements and coordinate / sign translation change request, in collaboration with other country roles (if applicable)
• Document and data management :
• Prepare documents and correspondence
• Collate, distribute / ship, and archive clinical documents, e.g. eTMF
• Assist with eTMF reconciliation
• Execute eTMF Quality Control Plan
• Update manuals / documents
• Document proper destruction of clinical supplies
• Prepare Investigator trial file binders
• Obtain translations of documents
• Regulatory & Site Start-Up responsibilities : Collaborate with other country roles to :
• In a timely manner, provide and collect from investigators forms / lists for site evaluation / validation, site start-up, and submissions
• Obtain, track, and update study insurance certificates
• Support preparation of submission package for IRB / ERC and support regulatory agencies submissions
• Budgeting, Agreement and Payments : Collaborate with finance / budgeting representatives to :
• Maintain contracts (e.g. CTRAs)
• Track and report contract negotiations
• Update and maintain contract templates (in cooperation with Legal Department)
• Monitor and track adherence and disclosures
• Maintain tracking tools
• Obtain and process FCPA documentation in a timely manner
• Meeting Attendance & Planning :
• Organize meetings (create & track study memos / letters / protocols
• Support local investigator meetings where applicable

Skills :

Experience Requirements :

Clinical Research, relevant healthcare or transferrable experience / skills preferred.

Educational Requirements :

High School Diploma or equivalent with completed job training (office management, administration, finance, life sciences, engineering, project management, healthcare, education preferred) required. Bachelor's Degree preferred.

Relocation : No

VISA Sponsorship : No

Travel Requirements : 10%

Flexible Work Arrangements : Remote

Shift : 1st - Day

Valid Driving License : No

Hazardous Material(s) : No

Job Posting End Date : 11 / 14 / 2025

Requisition ID : R372548