Clinical Trial Manager

3 weeks ago


Singapur, Singapore Parexel Full time

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 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. #J-18808-Ljbffr



  • Singapur, Singapore CTI Clinical Trial and Consulting Services Full time

    Overview Clinical Project Manager role at CTI Clinical Trial and Consulting Services. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the...


  • Singapur, Singapore Medpace Full time

    Join to apply for the Clinical Trial Manager (Oncology) role at Medpace Continue with Google Continue with Google Join to apply for the Clinical Trial Manager (Oncology) role at Medpace Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace...


  • Singapur, Singapore Parexel International Full time

    Key Accountabilities Trial Preparation Accountable for the trial activities for responsible R/OPU, including but not limited to; Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities. Creation, management and review of the R/OPU...


  • Singapur, Singapore Parexel Full time

    1 day ago Be among the first 25 applicants Key Accountabilities Accountable for the trial activities for responsible R/OPU, including but not limited to; Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities. Creation, management...


  • Singapur, Singapore Medpace Full time

    Job Summary Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials....


  • Singapur, Singapore IQVIA Full time

    Clinical Trial Manager (12-month contract) Responsibilities Leads the local/regional trial team in the capacity of Clinical Trial Manager (CTM) during trial preparation, conduct and close-out. Selected sites conduct and deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP and all other relevant...


  • Singapur, Singapore IQVIA LLC Full time

    Clinical Trial Manager (12-month contract) page is loaded## Clinical Trial Manager (12-month contract)locations: Singaporetime type: Full timeposted on: Posted Todayjob requisition id: R **Duties & Responsibilities:*** Leads the local/regional trial team in the capacity of Clinical Trial Manager (CTM) during trial preparation, conduct and close-out.*...


  • Singapur, Singapore IQVIA SOLUTIONS ASIA PTE. LTD. Full time

    Duties & Responsibilities: Leads the local/regional trial team in the capacity of Clinical Trial Manager (CTM) during trial preparation, conduct and close-out. Selected sites conduct and deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP and all other relevant external regulations. Lead and...


  • Singapur, Singapore SGP IQVIA RDS East Asia Pte Ltd. Full time

    Duties & Responsibilities: Leads the local/regional trial team in the capacity of Clinical Trial Manager (CTM) during trial preparation, conduct and close-out. Selected sites conduct and deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP and all other relevant external regulations. Lead and...


  • Singapur, Singapore IQVIA Full time

    Duties & Responsibilities Leads the local/regional trial team in the capacity of Clinical Trial Manager (CTM) during trial preparation, conduct and close‑out. Selected sites conduct and deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH‑GCP and all other relevant external regulations. Lead and...