艾昆纬
Clinical Lead/Local Trial Manager
Clinical Lead/Local Trial Manager
发布于 大约 6 小时前中层管理(经理/总监)
Taipei , Taipei City, Taiwan
高级经验
全职员工
仅现场办公
本科
Microsoft Office
ICH
Team Leadership
Problem Solving
Clinical Research
AI 估算 · 25k–40k
Senior clinical lead role at a top CRO, 5+ years experience, competitive market rate in Taiwan.
职位详情
关于这个职位
As a Clinical Lead at IQVIA, you will manage clinical trials from start to finish, ensuring compliance with GCP and regulatory standards. You lead a clinical team, collaborate with project leaders, and drive patient recruitment strategies to bring new drugs to market.
最低要求
Bachelor's Degree in health care or other scientific discipline required
Requires 5 years clinical research/monitoring experience or equivalent combination of education, training and experience
Requires basic knowledge of Project management practices and terminology
Requires good knowledge of applicable clinical research regulatory requirements i.e., GCP and ICH guidelines
Requires broad protocol knowledge and therapeutic knowledge
Requires good understanding of Clinical Research industry
Requires understanding of project finances
Knowledge of clinical trials and applicable regulatory requirements
Strong written and verbal communication skills including good command of English
Problem solving skills
Planning, time management and prioritization skills
Ability to handle conflicting priorities
Attention to detail and accuracy
Good influencing and negotiation skills
Good judgment and decision-making skills
Effective mentoring and training skills
Good software and computer skills including Microsoft Office
Ability to establish and maintain effective working relationships
Ability to work across geographies displaying cultural awareness
Ability to influence without authority
Demonstrate IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership)
工作职责
Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP, protocol), customer requirements (contract), and internal requirements (policies, SOPs, project plans).
Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.
Contribute to the development of the project risk mitigation plan and manage clinical risks through the project’s lifecycle.
Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline EAC and identify additional service opportunities or out of scope work.
Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
Conduct regular team meetings and communicate appropriately to achieve objectives.
Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.
May contribute to the development of the clinical delivery strategy for proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
May mentor and coach new peers as they assimilate into this role.
May work as a primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
May attend site visits as applicable in support of project delivery.
AI 洞察
优缺点分析
优点
- Work at a leading global CRO with extensive resources and career development opportunities.
- Gain exposure to cutting-edge clinical trials and drug development processes.
- Develop strong leadership and project management skills applicable across the industry.
- Competitive compensation and benefits typical of multinational companies.
- High responsibility and accountability for trial success, with tight timelines.
- Managing multiple stakeholders and cross-cultural teams can be demanding.
- Requires ongoing learning to keep up with evolving regulations and therapeutic areas.
- This role is ideal for experienced clinical research professionals who enjoy leading teams and managing complex projects, and who thrive in a fast-paced, regulated environment.
缺点 / 挑战
暂无明显挑战项
角色解读
- Advance to Senior Clinical Lead or Program Director overseeing multiple trials.
- Transition into global project leadership or clinical operations management.
- Specialize in therapeutic areas or move into business development / proposal roles.
- Oversee clinical trial delivery, ensuring compliance with regulatory and quality standards.
- Lead and manage clinical teams, including resourcing, training, and performance feedback.
- Develop recruitment strategies and manage project finances and risks.
- Collaborate with cross-functional teams and stakeholders to achieve project milestones.
- Deep knowledge of GCP, ICH guidelines, and local regulations.
- Strong project management and financial acumen.
- Excellent communication and leadership skills.
- Problem-solving and attention to detail.
申请策略
- Research IQVIA's therapeutic areas and align your experience with their focus.
- Prepare examples of how you've resolved complex clinical or stakeholder issues.
- Emphasize your experience managing full-cycle clinical trials and meeting recruitment targets.
- Highlight your leadership of clinical teams and any mentoring or training roles.
- Showcase your knowledge of GCP/ICH and regulatory submissions.
- Quantify results such as on-time delivery, budget management, or quality metrics.
- Strengthen project management skills through certifications like PMP.
- Enhance financial management knowledge (e.g., budgeting, EAC).
面试指南
- Use the STAR method (Situation, Task, Action, Result) to structure responses.
- Demonstrate leadership and proactive risk management.
- Highlight collaboration with cross-functional teams and external stakeholders.
- Describe a time you managed a clinical trial that was behind on recruitment. What steps did you take?
- How do you ensure GCP compliance across different sites and countries?
- Tell me about a conflict within your clinical team and how you resolved it.
- How do you prioritize multiple project demands and manage competing deadlines?
- What experience do you have with project financial management (e.g., EAC)?
匹配度报告
72
综合匹配度
Senior clinical leadership role at a top CRO with high social impact and growth, but on-site and potentially demanding.
适合人群
This role is best suited for candidates who prioritize meaningful work and career development over work-life balance.
最强匹配
使命价值匹配
最弱匹配
工作生活匹配
薪资福利75
成长发展80
工作生活50
使命价值85
薪资福利匹配
75中等
Compensation is competitive for a senior role at a global CRO, with standard benefits. Salary not disclosed, but likely market-aligned.
薪资信号未披露（AI估算：25K-40K/月）
成长发展匹配
80较高
Strong growth potential with exposure to global trials, leadership development, and mentoring opportunities.
技术前沿主流现代技术
技术栈Clinical Research、GCP、ICH、Project Management
成长机会mentor、coach、professional development、training
业务类型ambiguous
工作生活匹配
50较低
On-site role in Taipei, likely standard office hours, but trial demands may require flexibility and occasional travel.
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）
使命价值匹配
85较高
Meaningful work improving patient lives through drug development, with high social impact.
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improve patients’ lives、bring new drugs to the market faster
创新程度稳健跟随主流
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