高级临床数据科学家（仅限欧洲）
Sr Clinical Data Scientist (CDM- Europe Only)
高级临床数据科学家（仅限欧洲地区）
Syneos Health® 是一家领先的全面整合的生物制药解决方案组织，致力于加速客户成功。我们将独特的临床、医学事务和商业洞察转化为成果，以应对现代市场现实。
我们的临床开发模式将客户和患者置于我们所做一切的核心。我们不断寻找简化和优化工作的方法，不仅使 Syneos Health 更容易合作，也使我们更容易被合作。
无论您以功能服务提供商合作方式还是全服务环境加入我们，您都将与充满热情的问题解决者协作，作为团队成员不断创新，帮助我们的客户实现目标。我们敏捷且有动力加快疗法的交付，因为我们热衷于改变生命。
了解我们的 29,000 名员工在 110 个国家已经知道的事：
在这里工作，无处不在都重要
为什么选择 Syneos Health
- 我们致力于通过职业发展和晋升来培养员工；支持性强且积极参与的直线管理；技术和治疗领域培训；同行认可和全面奖励计划。
- 我们致力于打造“完整的自我”文化——您可以真实地做自己。我们的“完整的自我”文化将我们全球的员工团结在一起，我们致力于照顾好我们的员工。
- 我们持续打造我们所有人都希望工作的公司，也是客户希望合作的公司。为什么？因为当我们汇聚多样化的思想、背景、文化和视角时，我们能够创造一个让每个人都感到归属感的环境。
职位职责
***此职位仅开放在塞尔维亚招聘。
***需要具备 Veeva Vault 经验。
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担任临床数据科学的功能负责人，包括临床数据科学与项目管理、临床监查和其他职能组之间的内部联络人
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作为临床数据质量的中心负责人，通过对临床和操作数据的全面审查来监控风险，利用对方案的深入了解，考虑与所收集数据相关的特定治疗领域的方案方面，并与跨职能操作计划保持一致，以推动全面的临床数据质量
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确保识别所需的数据显示元素和相应的数据质量监督步骤，以支持定义的
查看英文原文
Sr Clinical Data Scientist (CDM- Europe Only)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job Responsibilities
***This position is only open to hiring in Serbia.
***Experience with Veeva Vault is required.
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Serves as Functional Lead for Clinical Data Science including primary contact for internal liaison between Clinical Data Science and Project Management, Clinical Monitoring, and other functional groups
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Acts as central steward of clinical data quality, monitors risks through the holistic review of clinical and operational data, using high level knowledge of the protocol, taking into account the specific therapeutic area aspects of the protocol related to the data collected and aligning with cross functional operational plans to drive comprehensive clinical data quality
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Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined study analysis
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Works with assigned project teams to communicate, address, troubleshoot and resolve data related questions and recommends potential solutions; escalates issues which potentially impact patient safety and study analysis
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Coordinates cross functional data cleaning activities to ensure quality standards and timelines are met for clinical data deliverables Ensures the required data elements and corresponding data quality oversight steps are identified to support the defined project analysis
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Drives the development of the clinical data acquisition plan and corresponding data flow diagram with the study team, assess risks associated with protocol design, study set parameters that could impact the credibility and reliability of the trial results, aligns data flow with the study protocol to ensure data collected meets regulatory and study endpoint requirements.
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Drives the development of analytical tools, utilizes analytical platform/dashboard to detect potentially unreliable data that may impact the validity of the trial results Performs analytic reviews as defined in scope of work and data acquisition plan, identifies root cause to systematically resolve data issues
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Monitors and communicates project progress to the Sponsor and project team including use of project status reports and tracking tools/metrics
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Ensures launch, delivery and completion of all Clinical Data Sciences activities and milestones according to contractual agreement and relevant Standard Operating Procedures (SOPs), guidelines, and regulations
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Review, maintain budget and identify out of scope for Clinical Sciences activities, raise to PM to be implemented in required change order
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Plans, manages, and requests Clinical Data Science resources for assigned projects
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Coordinates the work of the assigned Clinical Data Science team
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Develops and maintains project plans, specifications, and documentation in line with SOP requirements
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Maintains documentation on an ongoing basis and ensures that all TMF filing is up to date for necessary files
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Participates in, and presents at internal, Sponsor, third-party, and investigator meetings on behalf of clinical data science responsibilities
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Prepares input, and participates in proposal bid defense meetings and request for proposals on behalf of clinical data science responsibilities
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Plans for and creates necessary documentation to support internal and external audits; participates in such audits on behalf of clinical data sciences responsibilities
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Trains and mentors new or junior team members
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Maintains proficiency in Clinical Data Science systems and processes through regular training. May attend/represent the company at professional meetings/conferences
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Performs other work-related duties as assigned. Minimal travel may be required (up to 25%)
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Originally posted on Himalayas