远程工作雷达

临床研究经理助理

Associate Clinical Research Manager

职能支持限定地区(需当地身份)
公司Lifelancer
薪资$105,800 - $140,800/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

职位名称:临床研究经理(助理级)
工作地点:远程(美国)
工作地点类型:远程
工作合同类型:全职
职位级别:
BeOne 正以快速的速度持续增长,为有经验的专业人士提供具有挑战性和令人兴奋的机会。在考虑候选人时,我们寻找具有高度积极性、协作精神,并且最重要的是,对抗击癌症充满热情的科学和商业专业人士。
职位概述:
助理临床研究经理负责监督临床监测活动和CRAs团队的表现,以确保其符合ICH-GCP、当地法规和公司SOP,并在临床试验中保持质量。作为直线管理者,该职位通过提供指导、支持和发展机会,促进积极的团队文化,带领团队实现组织目标并确保高绩效。
岗位核心职责:
团队资源分配与绩效
分配CRAs资源并进行持续的资源评估,以确保工作量平衡,保证质量监控并满足研究交付要求。
确保CRAs具备必要的监控知识和技能,以高质量完成所需活动并满足研究交付要求。
根据ICH-GCP、SOP和当地法规,负责管理和解决CRAs的绩效和质量指标。
加强与研究中心的关系,以提升绩效并维护公司的试验交付声誉。

质量与合规
审查监控质量并解决问题,以确保符合监管指南、ICH-GCP指南和良好临床实践。
自2025年9月1日起生效
与跨职能团队合作,支持研究/研究中心里程碑的交付。
负责执行评估访问和陪同访问(如需要),以评估CRAs的持续监控能力,识别问题并制定解决策略。
参与流程优化项目,管理风险升级和解决。
支持研究中心审计/检查/现场合规访问(SCV),并确保对发现的问题采取纠正措施和后续跟进。
监督职责:
招聘与入职:执行招聘和雇佣活动,并协助新成员入职,以确保与团队目标和文化的契合。
任务分配:根据个人优势和团队目标分配任务,确保产品最优。

查看英文原文

Job Title: Associate Clinical Research Manager
Job Location: Remote (US)
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
BeOne 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.
General Description:
The Associate CRM oversees clinical monitoring activities and the CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve organizational goals and ensure high performance by providing guidance, support, and development opportunities while promoting a positive team culture.
Essential Functions of the Job:
Team Resource Allocation & Performance
Allocate CRA resources and perform ongoing resource assessments to ensure a balanced workload for quality monitoring and to meet study deliverables.
Ensure CRAs have the required level of monitoring knowledge and skills to successfully perform required activities with high quality to meet study deliverables.
Is responsible for managing and addressing CRA performance and quality indicators in accordance with ICH-GCP, SOPs and local regulations.
Strengthen site relationships to enhance performance and uphold the company’s trial delivery reputation.

Quality and Compliance

Review monitoring quality and resolve issues to ensure compliance with regulatory guidelines, ICH-GCP Guidelines, and Good Clinical Practices.
Effective September 01, 2025
Support study/site milestone delivery in collaboration with cross-functional teams.
Responsible for execution of assessment visits and accompanied visits (where required) to assess ongoing CRA monitoring competency, identifying issues and developing resolution strategies.
Contribute to process optimization initiatives and manage risk escalation and resolution.
Support site audits/inspections/Site Compliance Visits (SCV) and ensure corrective action and follow-up for identified issues.
Supervisory Responsibilities:
Recruitment and Onboarding: Performs recruiting and hiring activities, along with onboarding new team members to ensure alignment with team objectives and culture.
Task Assignment: Assign tasks based on individual strengths and team objectives, ensuring optimal productivity.
Support and Resource Provision: Support team members by providing necessary resources to help them effectively perform their roles.
Communication and Collaboration: Encourage open communication and collaboration within the team and with other functions, including acting as a point of contact for issue escalation and feedback where required.
Performance Evaluation: Conduct regular performance evaluations and provide constructive feedback to promote continuous improvement.
Mentoring and Development: Lead and mentor team members, fostering an environment of growth and development.
Issue Resolution: Address any personnel issues promptly and fairly to maintain a positive work environment.
Career Development Support: Support team members in identifying and pursuing professional development opportunities.
Computer Skills: Proficient in Microsoft Word, Excel, PowerPoint and Outlook
Other Qualifications:
Fluent in written and verbal English
Minimum 5 years of industry experience in the pharmaceutical or CRO or relevant field
Thorough understanding of the drug development process, including expert knowledge of international standards (ICH-GCP) and health authority requirements
Understanding of all aspects of monitoring and trial execution, with previous experience as a CRA preferred
Excellent interpersonal skills, strong organizational and effective written and verbal communication skills.
Experience in Oncology is highly recommended.

Travel: Be adaptable to business trips as required per business need; require valid driver’s license in applicable countries
Education Required:
Bachelor’s degree or higher in a scientific or healthcare discipline, and advanced degrees preferred.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, 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

Salary Range: $105,800.00 - $140,800.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne 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. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact .

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Originally posted on Himalayas

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