(Senior) Clinical Research Associate job opportunity at BeOne Medicines.

Home Jobs In South Korea Tag: Job (Senior) Clinical Research Associate position at BeOne Medicines


DatePosted 30+ Days Ago bot
BeOne Medicines (Senior) Clinical Research Associate
Experience: 3-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeAssociate
loacation Seoul, South Korea
loacation Seoul....South Korea

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: About the Company: BeiGene (NASDAQ: BGNE; HKEX: 06160; SHA: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical trial candidates, we are committed to expediting the development of our diverse pipeline of novel therapies through collaborations or our own internal capabilities, with the aspirational goal of radically improving access to medicines for billions more people by 2030. BeiGene is a headquarter-less company by design, with a growing global team of approximately 8,000 colleagues across five continents. Job Description • Conducts monitoring (pre study, initiation, routine monitoring and closeout visit), if require • Conducts co monitoring visits, if required • Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.) • Attends onboarding--, disease indication and project specific training and general CRA training as required • Documents monitoring activities appropriately following ICH GCP and BeiGene standards • Conducts Quality Oversight Visits (QOV), as requested • Completes monitoring visit/ QOV reports timely • Assists with investigator/site identification • Assists site to prepare Ethics Committee submissions • Facilitates clinical trial site contract and budget negotiation • Manages site queries and communications • Assists in managing clinical trials, if required • Establishes regular lines of communication with sites and COMs • Provides protocol and related study training to assigned sites • Evaluates the quality and integrity of site practices escalating quality issues as appropriate • Manages site performance by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution • Collaborates with CRA Group / CRM to ensure recruitment plans and execute contingency plans, as needed • Performs additional task as assigned Qualification Required: • Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical • Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines • 1-3 years or more (SCRA) monitoring experience in the pharmaceutical or CRO industry • Excellent communication and interpersonal skills • Excellent organizational skills and ability to prioritize and multi-task • Fluent in English (writing and speaking) What we offer to our valued employees: Market competitive compensation package including performance-based annual bonus scheme Company shares (generous welcome grant and performance-based annual equity plan!) In-house and external learning and development opportunities Fantastic benefits program as per the current policy including; Health Insurance provided Medical Check-up, flu vaccine reimbursement Home-office setup allowance Monthly reimbursement for home office expenses (i.e. internet, mobile..) Wellness benefits (Employee Assistance Program) Paid parental leave Annual leave Marriage leave and allowance, condolence leave and allowance And more as the benefit programs keep improving! Plus you get to work with a dynamic team of collaborative, supportive, diverse, and fun professionals whose mission is clear: Cancer has no borders and neither do we. BeiGene is proud to be an Equal Opportunity Employer: 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. BeiGene Korea Y. H. is committed to treating all applicants fairly and equally. As a Disability Confident employer, we will work with applicants to make any reasonable adjustments. 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 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 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 in Workday (currently located in the U.S.). Besides, job applicants’ data will be kept for one year 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.

Other Ai Matches

(Senior) Clinical Research Associate Applicants are expected to have a solid experience in handling Job related tasks
Manager or Senior Manager, Clinical Pharmacology & Pharmacometrics Applicants are expected to have a solid experience in handling Clinical Pharmacology & Pharmacometrics related tasks
(Senior) Medical Affairs Manager Applicants are expected to have a solid experience in handling Job related tasks
Account Manager - Solid Tumor (Pittsburgh, PA) Applicants are expected to have a solid experience in handling PA) related tasks
remote-jobserver Remote
Director, Senior IP Counsel, Small Molecule Applicants are expected to have a solid experience in handling Senior IP Counsel, Small Molecule related tasks
Senior Director, Field Medical Excellence (office based) Applicants are expected to have a solid experience in handling Field Medical Excellence (office based) related tasks
remote-jobserver Remote
Senior Manager, Post Trial Supply Applicants are expected to have a solid experience in handling Post Trial Supply related tasks
remote-jobserver Remote
Associate General Counsel, Head of R&D Legal Applicants are expected to have a solid experience in handling Head of R&D Legal related tasks
remote-jobserver Remote
Director, Global Regulatory Lead Applicants are expected to have a solid experience in handling Global Regulatory Lead related tasks
Medical Science Liaison/Sr. Medical Science Liaison, Solid Tumor Applicants are expected to have a solid experience in handling Solid Tumor related tasks
remote-jobserver Remote
Clinical Study Manager Line Manager Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Director, Global Value, Access & Pricing; Solid Tumors, Pipeline Applicants are expected to have a solid experience in handling Global Value, Access & Pricing; Solid Tumors, Pipeline related tasks
Marketing Executive Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Vice President, US Marketing, Oncology Applicants are expected to have a solid experience in handling US Marketing, Oncology related tasks
Senior Manager - Associate Director, Regulatory Affairs, Japan Applicants are expected to have a solid experience in handling Regulatory Affairs, Japan related tasks
(Senior) Manager, Clinical Site Budget Planning Applicants are expected to have a solid experience in handling Clinical Site Budget Planning related tasks
remote-jobserver Remote
Senior Manager, Publications Systems & Operations Applicants are expected to have a solid experience in handling Publications Systems & Operations related tasks
remote-jobserver Remote
Senior Director, Global Clinical Operations, Study Start-Up, Americas Applicants are expected to have a solid experience in handling Global Clinical Operations, Study Start-Up, Americas related tasks
Associate Director, Senior GBS Controller Lead Applicants are expected to have a solid experience in handling Senior GBS Controller Lead related tasks
remote-jobserver Remote
Senior Director, Oncology Program Management Applicants are expected to have a solid experience in handling Oncology Program Management related tasks
Director, GTS TechOps ERP Applicants are expected to have a solid experience in handling GTS TechOps ERP related tasks
remote-jobserver Remote
Clinical Research Associate Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Senior Manager, Advanced Analytics Applicants are expected to have a solid experience in handling Advanced Analytics related tasks