Jobs: clinical managers

该职位来源于猎聘 Purpose: To drive growth by (a) developing our business to achieve top line goals in assigned or break-in accounts, and (b) strengthening the organization’s partnership with existing and new clients Identifying appropriate targets and expand footprint among existing accounts and new accounts. Indegene is a specialized healthcare...

该职位来源于猎聘 外派Global Pharma Primary Responsibilities:  Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work, SOPs (and / or the Sponsor’s SOPs as appropriate) and the ICH GCP and associated regulations. May perform co-monitoring visits and other types of site...

该职位来源于猎聘 Clinical Research Associate performs site management, site administration and site monitoring responsibility for clinical studies according to Fortrea Standard Operating Procedures, ICH Guidelines and GCP, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of...

该职位来源于猎聘 Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government,...

该职位来源于猎聘 Key Responsibilities Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less sophisticated projects. Develops clinical tools...

该职位来源于猎聘 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking...

该职位来源于猎聘 Key Responsibilities: Allocate workload and site assignments within the clinical monitoring team. Ensure quality of the clinical monitoring deliverables within a project and maintain proper visibility of its progress by the use of tracking tools. May include the development of the Clinical Management Plan (CMP). Ensure efficient...

该职位来源于猎聘 FSP Global Pharma 招聘要求： - 统招本科及以上学历，医药学相关专业 - 2.5年及以上CRA经验，必须有肿瘤项目经验，有血液瘤项目经验优先 - 既往有外企CRO/pharma背景经验者优先 - 内驱力强，能抗压，主动快速学习能力强 -...

该职位来源于猎聘 Responsible for ensuring global regulatory reporting compliance by execution of processes and compliance with procedures for processing safety reports originating from clinical studies, literature, hotline, regulatory feedback data, social media and/or other sources for post-marketing products. Ensures timely identification of...

该职位来源于猎聘 Purpose of the Role: Purpose of Principal Medical Pharmacovigilance Scientist or Senior Medical Pharmacovigilance Scientist role is to monitor on the safety of patients participating in clinical trials and post marketing surveillance. This role involves the medical review and evaluation of adverse events, signal detection, risk...

该职位来源于猎聘 FSP global Biotech Job responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate...

该职位来源于猎聘 临床试验医生，研究领域 科室不限，有上市前临床试验相关经验者优先。 Job title: Clinician Job description: Co-chairs clinical study team and works collaboratively with other study team members. Point of accountability to the BU for design, conduct, interpretation and reporting of one or more clinical...

该职位来源于猎聘 FSP Global Pharma 肿瘤/非肿 (II期III期) Job responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and...

该职位来源于猎聘 Key responsibilities and skills may include, but are not limited to: Analyze data and report statistical results. Develop SDTM specifications for programming datasets following CDISC standard. Independently develop SAS programs to create SDTM datasets. Develop ADaM analysis data specifications for programming following CDISC...

该职位来源于猎聘 Primary Responsibilities: Responsible for overall clinical research activities for multiple pre- and post-approval studies, evidence generation and dissemination efforts, and budget oversight. Support the design of appropriate clinical trials to meet the clients’ needs Responsible for delivery of assigned clinical programs,...

该职位来源于猎聘 工作职责： A. 项目支持/Project Support: 1. 协助项目团队组织会议、记录会议纪要并跟进行动项。 Support project team by organizing meetings, documenting minutes, and tracking action items. 2. 协助准备和审核临床试验相关文件，如研究方案、病例报告表和研究报告等。 Assist in...

该职位来源于猎聘 Job Overview: Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a trial within contractual and...

该职位来源于猎聘 About the job Ready to push the limits of what’s possible? Join Sanofi and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world. As Early Detection Strategy and Patient Activation Lead within our Type I Diabetes business, you’ll integrate resources and...

该职位来源于猎聘 Syneos Core Team Opportunity JOB SUMMARY The Clinical Trial Manager (CTM) serves as the clinical functional lead, accountable for the delivery of site management, clinical monitoring and central monitoring of assigned study(ies). A CTM is expected to independently manage the clinical and central monitoring team members but may serve...

该职位来源于猎聘 Key Responsibilities： Oversee end-to-end clinical trial delivery, ensuring all milestones meet on schedule and within budget, via planning, organizing, and executing. Lead and coordinate cross-functional teams including medical, site management, data management, biostatisticians, and supply chains to ensure seamless collaboration...