Offer summary

Qualifications:

Bachelor's degree in a relevant scientific discipline., Minimum of 2 years of clinical monitoring experience., Fluent in English and German, both written and spoken., Knowledge of ICH guidelines and GCP for clinical trials..

Key responsibilities:

Perform monitoring activities at clinical trial sites to ensure compliance and data quality.

Collaborate with the Clinical Operations Manager to meet study timelines and standards.

Support site selection, initiation, and training processes.

Ensure inspection readiness and facilitate audits and inspections.

Job description

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:The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.
Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncologyhematology clinical trials within the assigned region.
The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.
Identify gaps and areas for improvement and propose CAPA.
Supports startup and provides local expertise.
SSU experience is considered a plus
CRA activities
Perform feasibility, site identification, selection and evaluation, supporting initial list of sites and recruitment targets
Provides protocol and related study training to assigned sites.
Conducts monitoring (prestudy, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs
Conducts comonitoring visits, if required
Completes monitoring visit reports in accordance with ICHGCP, BeOne Medicines standards and SOP
Manages sites and site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations
Ensure inspection readiness of the study and sites
Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.)
Attends disease indication project specific training and general CRA training as required
Facilitate Study Oversight Visits (SOVs), site audits andor inspections, as required
Evaluates the quality and integrity of site practices – escalating quality andor GCP issues with Investigators and internal team as appropriate.
Anticipate and identify site issues; propose corrective and preventative actions; identify gaps and utilize opportunities. Constantly strive for operating excellence, question statusquo and promote innovation.
Education Required:
BS in a relevant scientific discipline and minimum of 2 years of monitoring experience.
Experience in oncology global trials preferred
Other Qualifications:
Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
At least 2 years of (CRA) monitoring experience in the pharmaceutical or CRO industry
Experience in oncologyhematology trials preferred
Excellent communication and interpersonal skills
Excellent organizational skills and ability to prioritize and multitask
Fluent in English & German (writing and speaking)
Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook
Travel: up to 60%
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
SelfAwareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
ResultsOriented
Analytical ThinkingData Analysis
Financial Excellence
Communicates with Clarity
We are proud to be an equal opportunity employer. BeOne 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.