(protocols, ICF, data collection forms/plans/reports, monitoring plans, manual of operations, investigator training materials, clinical trials report, study forms, templates and monitoring reports, etc.) and trial conduct (oversee central archiving, study supply management, regulatory submissions and ...
The CTM is responsible for the planning, conduct, completion and reporting of clinical trials under supporting and supervision on a local OPU level according to all applicable regulations and general quality requirements. * Resource management
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CLINICAL RESEARCH ASSOCIATE AND TRIAL MANAGEMENT COURSES Are you passionate about clinical research and want to be part of a research team to conduct clinical trials? Want to be a clinical research manager in a pharmaceutical, CRO, or research hospital. You must have an associate’s or bachelor...
7.Will be part of a team responsible for defending the clinical development program before regulatory authorities. Provides scientific and clinical guidance to Biology, Toxicology, Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory, and Project Management staff. ...
The work that we do matters. Every day, the clinical trials that we run bring life-changing medicines one step closer to market. Aldona DiSandro Associate Specialist, Clinical Research, Monitoring Management “ Our Medical Writing team is at the forefront of innovating the clinical documentation pr...
• Work with manager or other CRDC management (if necessary) to give inpu t to project plans ...
Proven experience in risk management Contact: lucy.fu@danone.com 工作地址 上海 下一个:FA新媒体与运营实习生 霍露丝今日活跃 达能- HR 匹配度分析立即分析 三个月内共 87 位应聘者投递了该职位,您的简历与该职位的匹配度为:323 较低 一般 较为匹配 ...
Trial Execution: Ensure clinical trials are conducted per protocol requirements, ICH-GCP, and internal procedures. Set clear expectations and motivate team members and external partners to meet objectives. Independent Management: Operate with minimal supervision while ensuring effective commun...
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