Watch Jobs
Johnson & Johnson logo
强生
Associate Director, Clinical Research
立即应聘

Associate Director, Clinical Research

发布于 大约 3 小时前

中层管理(经理/总监)

Hong Kong, Hong Kong
高级经验
全职员工
仅现场办公
本科
临床研究
Clinical Research
Cross-Functional Collaboration
Leadership
Regulatory Affairs
Neurovascular

AI 估算 · 65k–110k

香港临床研究管理层，经验要求高，薪资竞争力强，强生平台加持，但未明确具体数字。

职位详情

关于这个职位

This leadership role at Johnson & Johnson MedTech Neurovascular oversees a team of clinical research professionals, managing clinical trials and executing evidence generation strategies for complex projects. You will lead cross-functional collaborations, ensure regulatory compliance, and drive clinical programs to deliver innovative treatments for stroke patients.

最低要求

Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

A minimum of 8 years related scientific/technical experience, including leadership/management role within Clinical Research.
Significant previous experience in clinical project leadership across multiple studies/programs is required.
Experience working well with cross-functional teams is required.
Experience with budget planning, tracking and control is required.

工作职责

Is responsible for the execution of Clinical R&D activities for multiple and/or complex projects.

Manages team of clinical research professionals to manage clinical trials.
Is responsible for clinical team’s interface and collaboration with key opinion leaders, investigators, IRBs/ECs, Regulatory agencies, contractors/vendors, societies, associations, and company personnel.
Provides inputs on the development and executes the delivery of appropriate Global Evidence Generation Strategies (EGS)/Evidence Dissemination Strategies (EDS) to support New Product Development and Life-Cycle Management for transformational/complex programs.
Foster collaborative relationships with all relevant Clinical R&D partners and cross-functional partners (e.g. Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access, R&D, etc), ensuring cross-functional alignment.
Coordinates input and alignment from key regional MD Clinical R&D leads and other countries/regions in the development of the EGS/EDS.
Leads study design to develop appropriate clinical trials to meet the clinical evidence needs.
Fosters strong working relationships with external stakeholders.
Partners with internal stakeholders to ensure accurate dissemination of clinical data/evidence in value briefs and technical summaries for market access and reimbursement.
Is responsible for delivery of assigned clinical programs, through effective partnership with internal/external stakeholders, to enable optimized engagement leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs).
Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders.
Monitors assigned project budgets to ensure adherence to globally defined business plans.
Leads clinical scientific discussions with regulatory agencies/notified bodies to drive support of the clinical and regulatory strategy, including proposed clinical investigations; review process of clinical evidence generated for marketing authorization, line extensions, etc, including during sponsor regulatory inspections, in line with global frameworks.
Serves as the clinical representative on a New Product Development team.
Is responsible for development of Post-Market Clinical Follow-up (PMCF) Plans and Reports, in line with global frameworks.
Conducts review of promotional materials to ensure fair-balance, accuracy in clinical claims and messaging.
Manages and mentors resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency.
Is responsible for providing performance feedback to direct reports (if applicable) as well as coaching and assistance in their development.
Responsible for communicating business related issues or opportunities to next management level.
Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
Performs other duties assigned as needed.

优先资格

Relevant industry certifications is preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR,…).

Clinical/medical background is a plus.
A minimum of 1-2 year people management related experience is a plus.
Medical device experience is highly preferred.

AI 洞察

优缺点分析

优点

  • Work for a global healthcare leader with strong impact on patient care.
  • Lead a dedicated team and shape clinical evidence strategies.
  • Exposure to cutting-edge neurovascular technologies.
  • High responsibility in managing complex clinical trials and regulatory compliance.
  • Requires balancing multiple stakeholders and tight budgets.
  • Individuals with extensive clinical research experience, strong leadership capabilities, and a passion for improving stroke care.

缺点 / 挑战

暂无明显挑战项

角色解读

  • Potential advancement to Director or Senior Director of Clinical Research.
  • Opportunity to lead larger global programs and influence medical device innovation.
  • Lead a team of clinical research professionals to manage clinical trials for neurovascular projects.
  • Develop and execute evidence generation and dissemination strategies (EGS/EDS) for complex programs.
  • Collaborate with key opinion leaders, regulatory agencies, and cross-functional teams to ensure trial success.
  • Deep expertise in clinical research processes and regulations.
  • Strong leadership and people management skills.
  • Experience in budget management and cross-functional collaboration.

申请策略

  • Research Johnson & Johnson's Neurovascular portfolio and recent product innovations.
  • Tailor your CV to demonstrate strategic thinking and people management.
  • Emphasize 8+ years of clinical research experience, especially leadership roles.
  • Highlight specific examples of managing multi-study programs and cross-functional teams.
  • Showcase budget planning and tracking accomplishments.
  • Familiarize with relevant industry certifications like CCRA, RACP, or ISO 14155.
  • Strengthen knowledge of regulatory requirements for medical devices (MDR, PMCF).

面试指南

  • Use the STAR method (Situation, Task, Action, Result) to structure answers, focusing on your specific leadership actions and measurable outcomes.
  • Describe your experience managing complex clinical trials across multiple sites.
  • How have you handled budget overruns in a clinical project?
  • Tell us about a time you collaborated with regulatory agencies or KOLs.
  • How do you mentor and develop junior clinical staff?
  • Prepare detailed examples of your project leadership, including challenges faced and solutions implemented.
  • Review Johnson & Johnson's Credo and its commitment to healthcare innovation.

职位点评

67
综合评分

医疗巨头的中层管理岗，社会价值高，薪资未披露，需现场办公。

从薪资福利、成长空间、工作节奏和岗位方向综合评估，方便横向比较。

更适合这类人
适合具有临床研究背景、渴望在医疗创新领域发挥领导作用并追求职业成就感的资深人士。
表现最好
使命价值
相对薄弱
工作生活
薪资福利65
成长发展75
工作生活50
使命价值85

薪资福利

65中等

薪资未在JD中提及，但强生作为跨国巨头通常提供有竞争力的薪酬和福利。

薪资信号未披露（AI估算：65K-110K/月）

成长发展

75中等

该职位提供团队管理经验，涉及项目领导、跨部门协作，并有指导下属的职责，有利于职业发展。虽未明确晋升路径，但作为Associate Director已有较高起点。

技术前沿非技术岗（不适用）
技术栈Clinical Research、Clinical Trials、Regulatory Affairs、Medical Devices、PMCF
成长机会mentors、coaching、development
业务类型ambiguous

工作生活

50较低

工作地点在香港，需现场办公，JD未提及远程或弹性工作安排。

工作模式仅现场办公
办公地点未明确
加班情况未提及（无法判断）

使命价值

85较高

职位专注于神经血管创新治疗，直接改善中风患者预后，社会价值显著。

行业发展稳定成熟行业
社会影响正向社会影响力较高
使命信号health is everything、improve health for humanity
创新程度积极采用新技术

强生 的其他在招职位

相似职位推荐

Watch Jobs