北京招聘

Essential Functions of the job:
Manage and contribute the GCP and GLP Quality Assurance activities:
?Conducting quality assurance (QA) activities related to CFDA and ROW regulations across therapeutic areas and provide GCP guidance for all phases of drug development
?Develop/improve and contribute quality systems and processes to include:
?Creation/revision of appropriate SOPs
?Supporting the activities related to the vendor management process training, SOPs, etc.
?Conducting routine and for cause audit of investigator site, vendors, internal audits, etc.
?Conducting review of key documents such as study protocols, informed consent documents, Investigator brochures, Clinical study reports, submission modules, etc.
?Management and review of trends and report significant investigation/deviation issues and system deficiencies to senior management, as appropriate
?Coordinate and/or administer GCP training, as needed
?Participate and represent Clinical Quality in meetings and discussions as needed
?Participate in the review of study related metrics (i.e; protocol deviation, etc.) as part of Quality Management Risk approach to identify gaps, trends and the need for process improvements.
?Manage the inspection readiness activities and participate in managing regulatory health authority inspections.
?Promote continuous improvement
?Expert knowledge of GCPs particularly FDA and ICH requirements
?Ability to resolve complex problems where analysis of situations or data requires an in-depth evaluation of various factors
?Superb attention to detail, excellent review skills and the ability to organize and manage multiple tasks in a fast-paced environment.
?Exercise sound and balanced judgment in ensuring that written procedures are followed and in evaluating quality systems, processes, procedures, plans and protocols for compliance
?Proven ability in setting strategy for and driving quality process improvement initiatives
?Strong global knowledge and understanding of international regulations applicable to the conduct of clinical trials and pharmacovigilance operations
?Other duties as assigned
职位要求：
Competencies:
Ethics - Treats people with respect; Inspires the trust of others; Works with integrity and ethically; Upholds organizational values.
Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently. Completes administrative tasks correctly and on time. Follows instructions and responds to management direction.
Communication - Listens and gets clarification; Responds well to questions; Speaks clearly and persuasively in positive or negative situations. Writes clearly and informatively. Able to read and interpret written information.
Teamwork - Balances team and individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed. Contributes to building a positive team spirit; Shares expertise with others.
Adaptability – Able to adapt to changes in the work environment. Manages competing demands. Changes approach or method to best fit the situation. Able to deal with frequent change, delays, or unexpected events.
Technical Skills - Assesses own strengths and development areas; Pursues training and opportunities for growth; Strives to continuously build knowledge and skills; Shares expertise with others.
Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan.
Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.
Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data.
Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully.
Project Management - Communicates changes and progress; Completes projects on time and budget.
Computer Skills :
?PC literacy required, MSOffice skills(Outlook, Word, Excel, PowerPoint)
Other Qualifications :
Communication & Interpersonal Skills
?Excellent verbal and written communication skills
?Ability to effectively collaborate in a dynamic environment
Significant Contacts
?Quality Assurance
?Clinical Operations
?Pharmacovigilance
?Clinical Business Operations
?Biometrics
?Medical Monitors
?Regulatory Affairs
?Interacts with all levels of BeiGene
Travel:
May require up to 30% travel

百济神州是一家立足于科学的全球性生物科技公司，专注于开发创新、可负担的药物，旨在为全球患者改善治疗效果，提高药物可及性。目前公司广泛的药物组合包括40多款临床候选药物。公司通过加强自主研发能力和合作，加速推进多元、创新的药物管线开发。我们致力于在2030年前为全球20多亿人全面改善药物可及性。百济神州在全球五大洲打造了一支超过8,000人的团队。