Oncology Clinical Research Associate: Drive Trial Impact

BeiGene Ltd.; United States; Remote; USD 80,000 - 105,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k)

Paid Time Off

Wellness

Job summary

BeOne Medicines Ltd. is seeking an experienced Clinical Research Associate to monitor oncology and hematology trials across the United States. You will perform site initiation, routine monitoring and closeout visits, ensure regulatory compliance, and support site contracts and budgets.

Travel up to 70% is required, with strong communication and organizational skills essential. Qualifications include a Bachelor's degree in life sciences or related field, 2+ years of CRC experience in oncology,

Qualifications

• At least 2 years of Clinical Research Coordinator experience in Oncology.
• Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines.
• Excellent communication and interpersonal skills.
• Excellent organizational skills and ability to prioritize and multi-task.
• Fluent in English (writing and speaking).

Responsibilities

• Monitors pre-study, initiation, routine monitoring and closeout visits per protocol.
• Maintains timely, quality data collection and site communications.
• Documents monitoring activities following ICH-GCP and BeOne standards.
• Assists with investigator/site identification and ethics submissions.
• Supports site budget negotiation and regulatory submissions.

Skills

Communication

Interpersonal skills

Organizational skills

Multitasking

English fluency

Education

Bachelor’s degree or above in life sciences, pharmacy, nursing or medical

Tools

Microsoft Word

Excel

PowerPoint

OneNote

Outlook

EMR

CTMS

Site File Management

Data management systems

Job description

BeOne Medicines Ltd. is seeking an experienced Clinical Research Associate to monitor oncology and hematology trials across the United States. You will perform site initiation, routine monitoring and closeout visits, ensure regulatory compliance, and support site contracts and budgets.

Travel up to 70% is required, with strong communication and organizational skills essential. Qualifications include a Bachelor's degree in life sciences or related field, 2+ years of CRC experience in oncology,