Junior clinical operations manager
Il y a 1 semaine
Brussels, BRU, Belgique
EORTC
Temps plein
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EORTC is looking for a Junior Clinical Operations Manager (JrCOM) to reinforce its team.
The junior Clinical Operations Manager works under the hierarchical supervision of Head of the Clinical Operations Department.
Objective
The objective of the Junior Clinical Operations Manager at EORTC is to support the planning, coordination, and execution of clinical studies in compliance with regulatory and organizational standards. This role aims to ensure operational excellence by assisting in study set-up, monitoring timelines, and maintaining quality across all study activities.. Additionally, the Junior Clinical Operations Manager contributes to continuous process improvement and adherence to best practices in clinical research. Ultimately, the role supports the successful execution of clinical research projects aligned with EORTC’s mission to advance cancer treatment.
Main responsibilities / Major Activities
Non-project related responsibilities
Contribute to improvement/development of clinical operations processes and tools according to individual competences and interest
Project related responsibilities as of study set-up:
Manages the operational aspects during start and conduct of the project, at any time, such as but not limited to:
Ensures adequate logistical and operational support to the study sites during the conduct of the study at any time
Supports site monitoring and control
Develops of study-specific guidelines and training for sites (e.g. pharmacy manual, lab manual)
Manages drug supply (e.g. follow-up on necessary supplies to sites
Manages human biological material (e.g. follow-up on sample kit supplies to sites and sample shipment from sites to central laboratories)
Follows up with collaborating intergroups regarding operational activities delegated to them
Communicates adequately with the various stakeholders and third parties on operational and logistical activities
Follows up on change management and escalates to Clinical Operations Manager, Project Manager and/or line manager, as appropriate
Maintains Trial Master File, Clinical Trial Management System and other tracking tools applicable to the study
Supports redaction of the study newsletters
Supports preparation of internal/external audits
Profile
Master’s degree in life sciences (biomedical sciences, pharmaceutical sciences…) with two years of experience in similar function
Team player who can work independently
Excellent communication skills
Able to prioritize adequately
Excellent knowledge of MS office tools
GCP certification is mandatory
Strong interest in EORTC mission
Excellent written and spoken English
Benefits
Permanent contract
Homeworking allowance
Reimbursement of public transport
Pension plan
Hospitalisation insurance and ambulatory care
Meal vouchers
Free parking
Wage according to our Non-Profit organisation status
30 days holidays (full time)
Hybrid working environment (from Belgium only)