赛诺菲
Clinical Research Director
Clinical Research Director
发布于 大约 15 小时前中层管理(经理/总监)
Vitry-sur-Seine, France
高级经验
全职员工
仅现场办公
博士
医疗、制药与临床研究
Leadership
Regulatory Affairs
AI 估算 · 60k–90k
法国临床总监职位，要求高、经验丰富，生物制药行业薪酬偏高，月薪约6-9万人民币。
职位详情
关于这个职位
作为临床研究总监，您将领导肿瘤学项目的临床试验策略，与跨职能团队合作推动药物开发
该职位要求深厚的肿瘤学背景和制药行业经验，负责从试验设计到监管提交的全过程
适合希望在大型生物制药公司中发挥领导作用、推动创新疗法上市的资深临床专家
最低要求
Oncology training (medical oncology or hematology/oncology fellowship) or MD with experience (4+ years) is required.
Pharmaceutical experience is required, 3+ years strongly preferred.
Experience in late-stage clinical development strongly preferred.
Demonstrated experience in clinical trial design and execution.
Proven track record of working effectively with multifunctional teams to achieve project milestones.
While industry experience is preferred, candidates with demonstrated excellence in academic clinical research and documented achievements may be considered with relatively less industry experience.
工作职责
Establishes or adapts clinical development plan for the program(s) including discussions with clinical investigators, advisors and regulatory authorities and plans contingencies.
Leads, supports and oversees the execution of clinical development and studies activities, including but not limiting to:
Authors abbreviated protocol.
Reviews the final protocol and protocol amendments.
Reviews the Informed Consent Form, Written Subject Information and Trial Disclosure Form.
Reviews the study specific committee charters. Leads study specific committees with operational support.
Leads the clinical interpretation of study results, contributes to clinical study reports and clinical summaries.
Provides effective clinical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine.
Participates and contributes to regulatory and safety documents and discussions:
Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans.
Contributes to the clinical sections of the NDA/CTD, Briefing packages for regulatory meetings, PSP/PIP.
Participates in Advisory Committee preparation.
Scientific data evaluation and authorship:
Authors clinical abstracts, presentations for conferences, and manuscripts, when appropriate.
Supports the planning of advisory board meeting. Presents and discusses development strategy and clinical study result with external investigators and advisory boards, as appropriate.
优先资格
Experience in late-stage clinical development strongly preferred.
Pharmaceutical experience 3+ years strongly preferred.
AI 洞察
优缺点分析
优点
- Work at a leading global biopharma company with AI-powered R&D innovation.
- Lead high-impact oncology trials that can transform patient lives.
- Access to extensive resources, cross-functional exposure, and career development programs.
- Competitive compensation package with comprehensive health and wellness benefits.
- High responsibility and pressure to meet regulatory and project milestones in a fast-paced environment.
- Requires deep expertise and continuous learning in rapidly evolving oncology landscape.
- International collaboration may require flexibility across time zones.
- Experienced clinical oncologists or MDs with pharmaceutical industry experience who want to lead drug development and shape clinical strategy.
缺点 / 挑战
暂无明显挑战项
角色解读
- Advance to Global Project Head or Senior Director roles within R&D.
- Opportunity to lead larger, more complex programs or move into executive leadership.
- Expand into translational medicine or regulatory strategy leadership.
- Lead the clinical trial strategy for oncology programs, including designing protocols and managing study execution.
- Collaborate with cross-functional teams like Clinical Operations, Biostatistics, and Regulatory to align development plans.
- Interpret clinical data, author study reports, and present results to internal and external stakeholders.
- Contribute to regulatory submissions (IND/NDA) and safety documents, ensuring compliance with standards.
- Deep expertise in oncology, particularly solid tumor biology, and clinical trial design.
- Proven experience in pharmaceutical clinical development, preferably late-stage.
- Strong leadership and ability to drive multifunctional teams to achieve milestones.
- Excellent communication in English for global collaboration with US and European teams.
申请策略
- Tailor your CV to demonstrate impact on project timelines and regulatory approvals.
- Prepare to discuss specific examples of overcoming challenges in clinical trials.
- Highlight your oncology training (fellowship) and years of clinical research experience.
- Emphasize late-stage development experience and successful trial design examples.
- Showcase cross-functional teamwork and leadership in achieving milestones.
- Include regulatory submission contributions and scientific publications.
- Deepen understanding of AI applications in clinical research if not already familiar.
- Strengthen knowledge of regulatory requirements for oncology products in EU and US.
面试指南
- Use STAR method: Situation, Task, Action, Result for behavioral questions.
- For technical questions, explain rationale and outcomes, referencing guidelines like ICH-GCP.
- Describe a clinical trial you designed and how you ensured its success.
- How do you handle disagreements with regulatory authorities or investigators?
- Tell us about a time you led a multifunctional team through a difficult milestone.
- What is your approach to integrating translational medicine insights into trial design?
- How do you stay updated on the latest oncology therapies and trial methodologies?
- Review Sanofi's pipeline and recent oncology publications.
职位点评
76
综合评分
Senior clinical leadership role in a top pharma with strong purpose, high compensation, and growth opportunities, but demands on-site presence and high dedication.
更适合这类人
This role is ideal for professionals who prioritize impact, growth, and compensation over work-life balance, and who thrive in a high-responsibility, innovation-driven environment.
表现最好
使命价值
相对薄弱
工作生活
薪资福利80
成长发展85
工作生活50
使命价值90
薪资福利
80较高
The role offers competitive compensation and comprehensive benefits including healthcare and parental leave, typical for a senior position in a large pharma company. Salary is likely above market average.
薪资信号偏高 (60K-90K/月)
福利待遇high-quality healthcare、prevention and wellness programs、at least 14 weeks’ gender-neutral parental leave
成长发展
85较高
Opportunities for growth are emphasized with promotions, lateral moves, and continuous learning. The role is at the forefront of AI-powered drug development, offering exposure to cutting-edge technology.
技术前沿前沿/新兴技术
技术栈AI-powered research、clinical development、oncology
成长机会opportunities to grow your talent、drive your career、promotion or lateral move
业务类型profit_center
工作生活
50较低
Position is on-site in Vitry-sur-Seine, France, with no mention of remote work. While benefits include wellbeing programs, the role demands high responsibility and likely intensive work periods.
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）
工作生活平衡prevention and wellness programs
使命价值
90较高
Directly contributes to developing life-changing oncology therapies, aligning with a strong patient-centric mission. Sanofi's focus on innovation and improving lives provides high meaning.
行业发展高速增长赛道
社会影响正向社会影响力较高
使命信号improve people's lives、chase the miracles of science
创新程度积极采用新技术
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