Regional Clinical Trial Management Associate

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description

Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical studies are executed per expected and specified quality standards, within timelines and budget

Builds solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager

Supports the alignment of regional deliverables with overall study goals under the direction of the Regional Clinical Study Manager

Essential Functions Of The Job
Regional Trial Support & Collaboration

Develops regional study management experience by supporting to oversee multiple aspects of clinical trial conduct including feasibility assessment, study start-up, document generation and review, tracking of samples and enrollment of study participants.

Acquires solid knowledge of clinical research operations, including interpretation and implementation of regulations/ICH guidelines

Supports the Regional Clinical Study Manager with set up and logistics of regional team meetings (agenda, minutes, ..)

Establishes good collaboration with Regional Clinical Study Manager, the Global Study Management Associate and other key stakeholders regionally and globally

As required, supports CRAs with various activities such as monitoring visit preparations, TMF filing, ..

Timelines, Planning and Execution

Creates and maintains regional/country level SharePoint folders for the study and regional study team distribution lists

Sets up the countries and sites in the region in the appropriate systems e.g. eTMF, CTMS, ..and makes sure information is kept up to date

Supports system access requests for the region/country and ensure these are managed appropriately across the study life cycle, supports user account management for users in region

Might support the local adaptation of global documents under supervision of the Regional Clinical Study Manager

May assist in the review of study-related documents as they relate to the supported clinical trials as delegated by the Regional Clinical Study Manager (e.g., Informed consent forms, regional Pharmacy Manual, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, CRF Completion Guidelines and other relevant regional study plans and charters)

Supports study start up in region/country in close collaboration with the regional study start up team and the Regional Clinical Study Manager

Supports the organization of study specific investigator meetings together with the Regional Clinical Study Manager and the Global Study Management Associate

Supports the TMF specialist with country/site level TMF creation and maintains the country/site level TMF including regular review and QC of TMF documents as per the study TMF QC plan

Helps resolving any regional/country specific issues related to clinical supplies in collaboration with relevant stakeholdersd

Supports the data cleaning activities and contributes to the follow up of outstanding information for region/country

Prepares site newsletters and other correspondence related to clinical trial conduct (eg, best practices and lessons learned, frequently asked questions) in collaboration with the study team

Might assist in resolution of routine study questions from clinical trial sites

Might support the maintenance of information for region/country in relevant public registries (e.g CT.gov)

Supports the Regional Clinical Study Manager with providing all relevant information from region/country to be included in the Clinical Study Report

Quality

Supports the identification of operational risks and works with the Regional Clinical Study Manager to recommend solutions for discussion with appropriate team leadership

Learns and shares best practices in clinical operations methodologies, systems and processes with the emphasis on quality and compliance

Might support the preparation of sites for quality assurance audits and inspections

Suggests improvements to enhance the efficiency and the quality of the work performed on assigned projects

Might support the development of local/regional tools, work