Clinical Research Associate at BeiGene

, , Germany -

Full Time

Start Date

Immediate

Expiry Date

20 Jul, 26

Salary

68900.0

Posted On

21 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical monitoring, ICH-GCP guidelines, Oncology clinical trials, Hematology clinical trials, Site management, Regulatory submissions, Data query resolution, Protocol training, Feasibility studies, Site selection, Monitoring visit reports, CAPA, Communication, Organizational skills, Microsoft Office, Project management

Industry

Biotechnology Research

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 oncology/hematology 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 start-up 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 (pre-study, initiation, routine monitoring and closeout visits per monitoring plan and applicable SOPs Conducts co-monitoring visits, if required Completes monitoring visit reports in accordance with ICH-GCP, 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 and/or inspections, as required Evaluates the quality and integrity of site practices – escalating quality and/or 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 status-quo 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 oncology/hematology trials preferred Excellent communication and interpersonal skills Excellent organizational skills and ability to prioritize and multi-task Fluent in English & German (writing and speaking) Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook Travel: up to 60% Salary Range EU: 55,100.00 EUR - 68,900.00 EUR 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 Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data 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. BeOne 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 11,000 colleagues spans six continents. To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn, X (formerly known as Twitter), Facebook and Instagram. For more information, please visit the link to explore job opportunities in China Mainland. China Mainland Job Posting At BeOne, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Driving Excellence Bold Ingenuity Collaborative Spirit

Responsibilities

The Clinical Research Associate is responsible for executing clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They collaborate with the Regional Clinical Operations Manager to ensure study timelines, data quality, and inspection readiness are maintained throughout the trial lifecycle.