BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals
Job Summary
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.
Support in the delivery of study start-up, initial and ongoing submissions within established timelines with high quality and in accordance with ICH/GCP, BeOne SOPs, and local regulations.
We are proud to be an equal opportunity employer and do 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.
Matching Summary
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.
Skills & Requirements
Must-have
Clinical study start-up management
Knowledge of ICH/GCP guidelines
Regulatory submissions preparation
Site feasibility and activation
Project timeline management
Document management and negotiation
Intermediate Microsoft Office skills
Nice-to-have
Fluent English communication
Spanish language skills
Collaborative and motivated mindset
Experience in hematology and oncology
Ability to streamline workflows
Strong organizational skills
Diligence in follow through
Key Requirements
Bachelor’s degree in scientific or healthcare discipline
Minimum 2 years clinical research experience
Experience in biotech, pharmaceutical, CRO or clinical site