About us

BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeiGene, please visit www.beigene.com and follow us on LinkedIn and X (formerly known as Twitter).

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.

Job Description:

General Description:

The CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials by ICH guidelines and GCP, local regulations, and applicable SOPs. The CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Oncology and Pharma clinical trials within the assigned region(country).Accountable for the study start-up timelines and delivery.

Essential Functions of the job:

Conducts monitoring (pre-study, initiation, routine monitoring, and closeout visit), if requireConducts co-monitoring visits, if requiredAssists with investigator/site identificationAssists site to prepare Institutional Review Board/Ethics Committee (IRB/EC) submissionsFacilitates clinical trial site contract and budget negotiationManages site queries and communicationsAssists in managing clinical trials, if requiredEstablishes regular lines of communication with sites and CSMsProvides protocol and related study training to assigned sitesEvaluates the quality and integrity of site practices – escalating quality issues as appropriateManage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Performs QC of Trial Master Files; creates, maintains, and closes out TMFs; is key in set up, conduct, and close out of ancillary services for BeiGene studiesIndependently deliver clinical start-up component of assigned sites with accountability for time, cost and quality for assigned activities, which include, but not limited to,Investigator/Site identification, including conduct feasibility activity to identify investigators and conduct site visit to confirm qualification for the required study.Prepare, review, submit and QC submissions to Institution Review Board (IRB) to obtain clinical trial authorizations and approvalsPrepare, review, and approve site level critical documents for IP release.Develop and finalize Country and Site-Specific ICFs.Perform site contract/ budget negotiation during start-up and maintenance phase. (If required)Review and finalize subject compensation rule and insurance as per local regulations.Review and translate subject recruitment materials as per local regulations if required.Assist CSMs in managing clinical trial during startup phase.Assist in maintain and update company-level investigator database.Establish, maintain and enhance relationship with key opinion investigators and sites.Proactively identify potential issues and seek improvement. Take initiative for issue resolution. Coordinate the risk management process encompassing proactive risk identification, evaluation (probability and impact) and mitigation plans.Performs QC of Trial Master Files; creates, maintains, and closes out TMFs; is key in set up, conduct, and close out of ancillary services for BeiGene studies.Perform other duties as assigned by management

Description for focusing on Japan:

Supports to build Japan organization and required process such as Local SOP and WI.Supports rCSM to perform county activity for new studies if required.Conducts Site Motivation visits.Prepares and supports PMDA inspection.Other tasks, if needed.

Supervisory Responsibilities:  Not applicable

Qualification Required:

Education Required:

BS in a relevant scientific discipline and at least 3 years or more (CRA) monitoring experience in the pharmaceutical or CRO industryExperience in oncology global trials preferred

Computer Skills: Efficient in Microsoft Word, Excel, Outlook and other common software.
 

Other Qualifications:    

Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelinesAt least 3 years or more (CRAII) monitoring experience in the Pharmaceutical or CRO industryExcellent communication and interpersonal skillsExcellent organizational skills and ability to prioritize and multi-taskFluent in English (writing and speaking)
 

Travel:  up to 40-70% time, as required

What We Offer To Our Valued Employees

Market competitive compensation package including performance-based annual bonus schemeCompany shares (generous welcome grant and performance-based annual equity plan!)In-house and external learning and development opportunitiesFantastic benefits program and keep improving!Plus you get to work with a dynamic team of collaborative, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.Join us and Make momentum in your career!

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

BeiGene is committed to respect and protect personal information rights of job applicants and will process job applicants’ personal information in accordance with applicable laws and regulations.

Due to BeiGene’s global operation, job applicants’ data will be stored overseas with adequate protection. Besides, job applicants’ data will be stored for no longer than is necessary to facilitate potential application for other suitable positions in BeiGene. For further details, please refer to BeiGene’s Job Applicant Privacy Policy (https://www.beigene.com/privacy-policy).

If you voluntarily provide your personal information to us, it is deemed as you have acknowledged and consented to (if required by the applicable laws) BeiGene’s Job Applicant Privacy Policy as well as the relevant privacy terms. If you voluntarily provide the personal information of other job applicants to us, it is deemed as you have ensured that the relevant individuals have acknowledged and consented to (if required by the applicable laws) BeiGene’s Job Applicant Privacy Policy as well as the relevant privacy terms.

If you have any concern, please DO NOT provide any resume or other personal information to us.