时间运营经理
TIME Operations Manager
对精准医疗和推动医疗行业发展充满热情吗？
近年来底层技术的进展终于使人工智能能够以有意义的方式影响临床护理。Tempus 的专有平台连接了整个现实世界证据生态系统，为医生提供实时、可操作的见解，提供关于正确患者在正确时间接受正确治疗的关键信息。
你是否认为药物研发的速度太慢？是否准备好利用前沿技术加速癌症临床试验的完成？是否热衷于改善患者获取新治疗方案的机会？我们正在寻找一位具有创新想法并渴望将其付诸实践的制药行业客户经理。
你将负责：
- 维护并拓展与制药合作伙伴/CRO 的合作，采用创新方法实现快速研究启动
- 监督部分制药客户的交付工作，重点关注质量和高效的时间表
- 管理 TIME 网络内研究的日常执行，从研究启动到结束，确保客户满意度和 Tempus 业务的持续增长
- 利用对临床试验开发和研究启动的知识，使一系列试验准备好接入我们的站点网络
- 协助团队创建创新策略、流程、工具、系统和方法，以持续加速癌症临床试验的完成
- 与 Tempus 内部的多个团队协作，执行关键交付成果，包括站点运营、医学事务、病理学、生物信息学和数据科学
- 识别所负责研究的风险，并与内部和外部合作伙伴共同解决问题
资格要求：
- 偶尔需要出差（根据项目而定）
- 本科学历，4 年以上从站点、申办方或 CRO 角度参与复杂临床试验的经验
- 对 FDA 法规、GCP、研究启动、临床试验协议、试验预算、IRB 提交和制药运营有最高水平的了解
- 卓越的团队协作能力
- 优秀的客户服务技能，以及强大的人际沟通和问题解决能力
- 有设定并达成高标准绩效的显著记录
- 高度有条理且系统化，注重细节，能够高精度地完成任务，并具备前瞻性思维
查看英文原文
Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Do you find the slow pace of drug development unacceptable? Are you ready to use cutting-edge technology to accelerate the completion of cancer clinical trials? Are you passionate about improving patient access to new treatment options? We are looking for an Account Manager, Pharma, possessing innovative ideas and a desire to put them into action.
What you’ll do:
- Maintain and expand collaborations with pharmaceutical partners/CROs to employ an innovative approach to rapid study start-up
- Oversee the execution of deliverables for a subset of pharma clients with a focus on quality and expeditious timelines
- Manage the day-to-day execution of studies within the TIME network from study start up through closure ensuring customer satisfaction and ability for continued growth of Tempus business
- Utilize knowledge of clinical trial development and study start-up to get a portfolio of trials ready for our network of sites
- Assist team in creation of innovative tactics, processes, tools, systems, and strategies to continually accelerate the completion of cancer clinical trials
- Collaborate with various teams within Tempus, to execute key deliverables including site operations, medical affairs, pathology, bioinformatics and data science.
- Identify risks to assigned studies and work with internal and external partners to resolve issues
Qualifications:
- Occasional Travel required (will vary by project)
- Bachelor's Degree and 4+ years of experience in working with complex clinical trials from a site, sponsor or CRO perspective
- Highest level knowledge of FDA regulations, GCP, study start-up, clinical trial agreements, trial budgets, IRB submission and pharma operations
- Collaborative team player
- Exceptional customer service skills and strong interpersonal and problem solving skills
- Proven track record of setting and achieving high personal standards of performance
- Highly organized and systematic, superb attention to detail, and ability to complete tasks with a high degree of accuracy and an eye towards process improvement
- Flexible and adaptable; ability to work independently in a fast-paced environment
Preferred Qualifications:
- Experience with rapid site activation
- Experience with a research networks
- Clinical research project management experience
$65,000-$100,000
The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Originally posted on Himalayas