(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

Executive Director, Corporate Brand & Reputation Applicants are expected to have a solid experience in handling Corporate Brand & Reputation related tasks
Summer Internship: Quality Assurance Compliance Intern (Onsite - Hopewell, NJ) Applicants are expected to have a solid experience in handling NJ) related tasks
Sr. Project Manager, Clinical Biomarker Applicants are expected to have a solid experience in handling Clinical Biomarker related tasks
Senior Manager or Associate Director, Lifecycle RA Applicants are expected to have a solid experience in handling Lifecycle RA related tasks
EDC Administrator II Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Senior Manager, Global Labeling Compliance & Connectivity Applicants are expected to have a solid experience in handling Global Labeling Compliance & Connectivity related tasks
Clinical Research Associate Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Clinical Pharmacology and AI/ML Modeling Intern (Winter and Spring Quarter) Applicants are expected to have a solid experience in handling Job related tasks
(Senior) Medical Affairs Manager Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Key Account Manager Solid Tumors – Riyadh Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Senior Manager, Global Stock Plan Administration Applicants are expected to have a solid experience in handling Global Stock Plan Administration related tasks
Associate Director/Senior Manager, Business & Strategic Planning & Operations (JAPAC) Applicants are expected to have a solid experience in handling Business & Strategic Planning & Operations (JAPAC) related tasks
remote-jobserver Remote
Executive Medical Director, Safety Franchise Area Lead Applicants are expected to have a solid experience in handling Safety Franchise Area Lead related tasks
remote-jobserver Remote
Clinical Research Manager Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Regional Clinical Study Manager Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Summer Internship: Procurement Systems Intern (Remote) Applicants are expected to have a solid experience in handling Job related tasks
Clinical Research Associate (All level) Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Business Operations Director, Germany Applicants are expected to have a solid experience in handling Germany related tasks
remote-jobserver Remote
Summer Internship: Corporate Affairs Intern (Remote) Applicants are expected to have a solid experience in handling Job related tasks
remote-jobserver Remote
Executive Director, Global Infrastructure and Cloud Computing Applicants are expected to have a solid experience in handling Global Infrastructure and Cloud Computing related tasks
Senior Payment Accountant Specialist Applicants are expected to have a solid experience in handling Job related tasks
Senior Legal Counsel, Latin America Applicants are expected to have a solid experience in handling Latin America related tasks
remote-jobserver Remote
Associate Director, Regional Clinical Study Management Applicants are expected to have a solid experience in handling Regional Clinical Study Management related tasks