BeiGene 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 budgetBuilds solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study ManagerSupports 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 guidelinesSupports 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 globallyAs 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 listsSets up the countries and sites in the region in the appropriate systems e.g. eTMF, CTMS, ..and makes sure information is kept up to dateSupports 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 regionMight support the local adaptation of global documents under supervision of the Regional Clinical Study ManagerMay 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 ManagerSupports the organization of study specific investigator meetings together with the Regional Clinical Study Manager and the Global Study Management AssociateSupports 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 planHelps resolving any regional/country specific issues related to clinical supplies in collaboration with relevant stakeholdersdSupports the data cleaning activities and contributes to the follow up of outstanding information for region/countryPrepares site newsletters and other correspondence related to clinical trial conduct (eg, best practices and lessons learned, frequently asked questions) in collaboration with the study teamMight assist in resolution of routine study questions from clinical trial sitesMight 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 leadershipLearns and shares best practices in clinical operations methodologies, systems and processes with the emphasis on quality and complianceMight support the preparation of sites for quality assurance audits and inspectionsSuggests improvements to enhance the efficiency and the quality of the work performed on assigned projectsMight support the development of local/regional tools, working instructions and SOPs

Budget

Supports set up of vendors for activities outsourced in region/countrySupports management of regional study budget incl PO set upSupports PO set up for regional vendors

Education Required:  Bachelor’s Degree in a scientific or healthcare discipline required*, Higher Degree preferred

*exceptions might be made for candidates with relevant clinical operations experience

Supervisory Responsibilities:  

N/A

Computer Skills:    

MS Office

Other Qualifications:  

Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processes1 or more years of experience in clinical research within biotech, pharma or CRO industry

Travel: Limited travel might be require

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with Clarity

We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.