合规顾问/高级顾问 - RIM/Veeva业务分析师（美国时区）
Regulatory Consultant/Sr. Consultant - RIM/Veeva Business Analyst (US timeshift)
合规顾问/高级顾问 - RIM/Veeva业务分析师（美国时区轮班）
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，也使我们更容易被雇佣。
无论您通过功能服务提供商合作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合作，作为团队进行创新，帮助客户实现目标。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情：
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；支持性的、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 Total Self 文化——您可以真实地做自己。我们的 Total Self 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属于自己的环境。
职位职责
一般职责：
- 寻找具有 RIM/Veeva 经验的系统/流程导向分析师。
- 优秀的沟通能力和利益相关者管理技能。
- 硕士学位，整体 8 年以上经验。
- 具有系统需求收集、验证和用户验收测试的经验。
- 能够跨职能团队（法规运营、IT、流程开发等）协作。
注意：
- 排除仅具有法规出版/提交经验的候选人。
- 有 EST 时区的可用性，用于协作。
核心职责：
- 作为法规运营团队与 IT/工具管理团队之间的主要联络人。
- 聚焦于技术赋能和流程优化。
- 收集并记录需求
查看英文原文
Regulatory Consultant/Sr. Consultant - RIM/Veeva Business Analyst (US timeshift)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
General Responsibilities:
- Look for system/process-focused analysts with RIM/Veeva experience.
- Excellent communication and stakeholder management skills.
- Master’s degree with overall 8+ years’ experience
- Experience in system requirement gathering, validation, and user acceptance testing.
- Ability to collaborate across cross-functional teams (Reg Ops, IT, Process Development etc).
Note:
- Exclude candidates whose experience is limited to regulatory publishing/submissions.
- Availability in EST timezone for collaboration purposes.
Core Responsibilities:
- Act as the primary liaison between Regulatory Operations teams and IT/Tool Management teams.
- Focus on technology enablement and process optimization.
- Gather and document requirements from key users (business partners, RIM superusers, technical leads).
- Ensure requirements are maintained and updated in alignment with business needs.
- Collaborate with DTE and Validation teams.
- Support user testing activities, including preparation of test scripts and execution oversight.
- Serve as SME for RIM systems.
- Provide guidance, communication, and training to users on business tools and processes.
- Work closely with IT and process development teams to manage RIM system enhancements.
- Collaboration with global teams to coordinate system inputs, validate data, resolve missing fields or gaps, and support end-to-end system workflows.
- Contribute to continuous improvement initiatives.
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