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Sr Clin Ops Specialist

职能支持限定地区(需当地身份)
公司Syneos Health India Private Limited
薪资未公开
工作地点South Africa
地域资格限定地区(需当地身份)
时区要求日间重叠约 3 小时,需偶尔早起或晚睡
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 South Africa 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

临床解决方案团队成员以药物开发思维方式行动,应用多年的经验和深入专业知识来真正了解客户需求并代表我们塑造的解决方案中的创新者。我们在医疗技术领域开展了研究,帮助他们实现新的发展目标。无论你是加入我们的功能服务提供商合作伙伴关系还是全服务环境,你将与热情解决问题的人员合作,作为一个团队创新帮助客户实现他们的目标。我们都灵活和驱动于为彼此,我们的客户以及最重要的是需要的人提供。了解未来25,000名同事已经知道:为什么 Syneos 健康 • 我们热衷于通过职业发展和进步来培养我们的员工;支持性和参与的线路管理;技术和治疗领域培训;同行认可和总奖励计划。• 我们致力于建立一个包容性文化,让你真正成为自己。我们在此的核心是我们的目标:推动提供服务,这吸引了同事们每天展示和塑造能够显著影响某人的生活的解决方案的热情。• 我们不断地建设我们所有人都想为公司工作而客户都希望与他们合作的公司。为什么?因为我们知道当我们汇集来自世界各地的智能同事时,我们可以塑造医疗保健的未来,促进客户的影响并定义患者进步速度。·负责按照适用的公司和临床运营政策,标准操作程序和工作说明进行活动。·协助临床监测人员开展现场管理活动,包括担任项目研究的网站赞助商代表,并与网站沟通以确保遵守协议要求,学习程序和相关指南。·创建和协助维护项目的文件,处理项目信件。·参与档案审计。·编制和维护现场手册,参考工具和其他文档。· 保持,更新和输入临床跟踪信息到数据库中 · 收到的追踪信息

查看英文原文

Sr Clin Ops SpecialistSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

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 deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:
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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities

  • Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions.
  • Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines
  • Creates and assists with maintenance of project files, handles project correspondence
  • Participates in file audits
  • Prepares and maintains site manuals, reference tools and other documents
  • Maintains, updates, and inputs clinical tracking information into databases
  • Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client
  • Manages shared mailbox, processes site requests and routes correspondence appropriately
  • Coordinates the ordering, packaging, shipping and tracking of site supplies and materials
  • Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items
  • Routinely anticipates, identifies and resolves potential issues and implements corrective actions, seeking guidance as needed to resolve more complex issues
  • Maintains overall awareness in the field of clinical research, as well as assigned areas, by completing all necessary and assigned training.
  • May provide training or mentorship to more junior level Clinical Operations Specialists (COS).

Qualifications

  • Associates degree preferred or equivalent
  • Experience in clinical research/pharma/biotech or related field considered In lieu of degree
  • Good knowledge of medical terminology, clinical data, and ICH/GCP preferred
  • Ability to successfully prioritize and work on multiple tasks
  • Strong attention to detail, accuracy and organizational skills
  • Excellent communication, presentation, and interpersonal skills
  • Ability to embrace new technologies
  • Minimal travel up to 10% may be required

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

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