以上为北京时间。链接检查不代表仍在招聘，申请前请以招聘官网为准。
按这个岗位的城市和方向提醒，确认后才开启，可选择每日或每周。
领导项目管理及CRA团队，负责临床试验的进度、质量、预算和风险管控；管理CRO和供应商，确保合规并推动项目交付。
This role is responsible for leading the team of project management and (or) CRAs if applicable. Including but not limited to the project timeline control, oversees the key deliverables, and project milestones for ongoing clinical trials.
When needed, this role will also be responsible for the development and management of a portfolio of projects and/or programs, with respect to the delivery of quality project management services.
l Lead the project management and (or) CRAs team including in-house team members and Contract Research Organizations (CROs), vendors and other suppliers to ensure study quality, timeliness and adherence to budget.
l Meet with team members on a regular basis regarding project tasks to ensure project achievements.
l Monitor the status and make changes as needed to meet the deliverables of the trial.
l Assess, identify and monitor trial-level risks. Incorporate scientific knowledge, trial process, and expertise to create one integrated trial-level risk mitigation and contingency
plan.
l Identify and facilitate resolution of complex study problems and issues proactively.
l Create and monitor the overall budget and assumptions using financial tracking tools.
l Manage CRO qualification process, selection, and oversight to ensure that all clinical trials’ execution with SOP and local laws and regulations.
l Manage CRO and site budgets, communicate deviations from budget projections, and propose solutions for budget deviations.
l Support with cross-functional team to facilitate the trial protocol development and maintenance process.
l Collaborate with supply Chain team to develop and complete of the request and management for Clinical Supplies.
l Provide input to process development and improvement.
l Work with the internal quality control and site to ensure high quality of trial.
l Conduct QCV or CO-monitoring visit if needed;
l Plan and lead activities associated with audits and regulatory inspections.
l Develop and actively manage clinical trial recruitment strategies with evaluation of actual enrollment against assigned targets and working with investigational sites to meet, and whenever feasible, exceed enrollment targets.
l Develop and coordinate country level operational plans for a clinical study or multiple clinical studies within a development program (i.e. study timeline projection, drug and budget forecast, safety plan, monitoring plan, study management plan, issue escalation and resolution plan).
l Ensure that work is conducted in compliance with professional standards and meet quality and timeline metrics. Ensures compliance with SOP's, GCP and ICH
guidelines.
l Bachelor Degree, biological science or healthcare-related field, Master Degree or higher is preferred.
l Minimum 8 years of experience in Clinical Operations or other related fields with minimum 5 years of project management experience
l Minimum of 2 years of experience as CRA/SCRA
l Clinical research background, with medical and scientific knowledge preferred
l Excellent knowledge of spoken and written English.
l Working knowledge of MS Office suite and MS Project or equivalent
l Strong communication and presentation skills
l In-depth knowledge of applicable clinical research trails regulatory requirement (i.e：GCP and ICH guideline)
Competencies:
1． Solid problem solving andtime management skills
2． Excellent verbal and written skills
3． Great interpersonal skills
4． Strong attention to detail
5． Highly organized
6． Ownership and result driven
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