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Clinical Trial Manager - FSP

Singapore City, Central Singapore, Singapore 职位编号 R0000035536 类别 Clinical Trials
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关于这个职位

Key Accountabilities:

Operational Excellence

  • Check quality of TMF team deliverables (e.g. TMF overview compliance with process and system steps, quality of queries) and propose appropriate remedial actions
  • Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, and Parexel SOPs
  • Participate in Parexel and department system/standards improvement activities
  • Liaise with functional senior management to provide and collect feedback on the process implementation  
  • Support the development of SOPs and tools with Process Owners as necessary  
  • Create and modify new/existing materials/job aides for TMF operations
  • Serve as internal Subject Matter Expert for Parexel project teams, providing guidance and support during project implementation 
  • Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, travel expense claims)

Business & Financial Management

  • Provide consultation, facilitate metrics collection and develop action plans in conjunction with Management/Project Leadership/Leads to keep projects on time and within budget
  • Support development of materials and plans for TMF business opportunities and maintain the relevant libraries

Personal Ownership

  • May be responsible for own assignments as SME. This includes taking the role of a senior level contributor on a project/account team and ensuring high quality and timely delivery of own deliverables.

Skills:

  • Demonstrated ability to successfully manage the tasks.
  • Excellent interpersonal, verbal and written communication skills (including experience in making presentations at conferences, meetings, training sessions).
  • Advanced client focused approach to work.
  • A flexible attitude with respect to work assignments and new learning.
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
  • Ability to work in a matrix environment and to value the importance of teamwork.
  • Excellent negotiation skills.
  • Advanced in networking
  • Excellent analytical and problem-solving skills.
  • Ability to provide guidance to other stakeholders as required.

Knowledge and Experience

  • Substantial trial master file coordination experience or equal experience in clinical

Education:

  • Educated to a degree level (biological science, pharmacy or other health related discipline preferred) or relevant clinical or business equivalent
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