Skip to content
SIMZ Pudong, Shanghai
Permanent
Endpoint Technical Project Manager Position Overview: The Project Manager is the primary client interface for client implementations, from initial engagement to final launch. Project Managers are responsible for managing projects through the software development lifecycle while working collaboratively with teammates and maintaining exceptional client satisfaction. Responsibilities: Act as primary point of contact for clients, keeping them apprised of all project developments while maintaining ste
8/14/2022 11:02:05 AM
Zhangjiang Hi-Tech Park, Shanghai
Essential Job Duties: Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Responsibilities: Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely
Essential Job Duties: Participates in process improvement activities across Company Contributes or may lead the development of Company policies and processes involving medical, safety and therapeutics Identifies potential areas for improvement in departmental processes Partners with Global Clinical Operations to develop new, and enhance existing, client relationships Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team Leverages known, an
8/14/2022 11:02:04 AM
? Assist with the development of training programs to ensure staff, project and technical, achievement of position competencies. Present training programs to the technical staff regarding study build, change control and/or CRF Design. ? Assist in the development and implementation of solutions to global technical service issues/concerns regarding Medidata Rave or Oracle InForm or SAS or Other proprietary software including proactive prevention strategies. ? Provide support to Data Management for
The scope of this position is within one site across multiple studies daily. Assess and document clinical observations, body weight data, food consumption data, environmental data, and other data on the appropriate data collection system (or by hand when necessary). Understand and interpret a protocol. Recommends modifications in test methods or procedures. Perform study management, data organization, QA audit response, internal and external client communication skills, and quality check procedur
Essential Job Duties: 1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support 2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs 3) Complete minute taking and documentation for sponsor/external or internal teleconferences as requested 4) Assist in setting up and maintaining tracking systems/spreadsheet for eg study supplies 5) Maintain the Project Directory 6) Provid
outsourced facilities on site engineer support hard and soft service for SHA facilities Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
8/14/2022 11:02:03 AM
Chaoyang District, Beijing
Essential Job Duties The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the project p
8/12/2022 8:30:03 AM
Incumbent performs established procedures for clinical testing as required in all assigned laboratory disciplines. Incumbent is responsible for analyzing specimens whose results are then reported to the sponsor. Incumbent proactively seeks out opportunities to improve processes and procedures and demonstrates initiative in resolving problems. Supports quality control/quality assurance monitoring programs, and is responsible for assisting with training of personnel. Essential Functions Quality Con
8/11/2022 11:03:55 PM
Job Summary: Independently performs activities related to Project management process by coordinating activities for routine studies in compliance with appropriate protocol, Standard Operating Procedures (SOPs) and regulatory agency guidelines, in a timely, efficient, and quality manner. A. Essential Job Duties: Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules with some oversight, using proposal outline or client-supplied information. Responsible for
8/11/2022 11:02:15 PM
Suzhou, Shanghai
Hardware Maintain and support existing technology Research and test new technology Upgrade hardware as new technology is required Manage purchases and investment in hardware Software Process code promotions from vendors Test software changes in development Create production install plan and execute Remote Order Fulfillment Manage and maintain work order fulfillment server Manage software issues and changes Manage hardware updates and replacement Support operation team with expertise Business Cont
8/11/2022 11:02:12 PM
Guangzhou, Guangdong
I. Essential Job Duties: 1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 3) Responsible for all aspects of site management as prescribed in
8/11/2022 11:00:40 PM
I. Essential Job Duties: 1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 3) Responsible for all aspects of site management as prescribed in
8/11/2022 10:57:21 PM
Responsibilities Organizes, conducts and evaluates analytical results and testing. Maintains study documentation and laboratory records. Independently sets-up, maintains, operates and performs routine and non-routine maintenance on general equipment, including problem identification and resolution. Performs quality control review of data. Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect integrity of the data; participates in correc
8/11/2022 10:56:54 PM
I. Essential Job Duties: 1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 2) Responsible for all aspects of site management as prescribed in the project plans 3) General On-Site Monitoring Responsibilities: 4) Ensure the study staff who will conduct the protocol have received the proper materials and instruct
8/11/2022 10:54:33 PM
Demonstrate the ability to give clear and accurate instructions to the staff Demonstrate the ability to multi task Demonstrate the ability to troubleshoot and resolve problems effectively. Identify and resolve workflow issues Organize meetings with others to discuss workflow and pending issues as well to prioritize any critical task Directs and or re directs team members to accommodate volume changes and client deadlines Demonstrates flexibility by doing other duties as assigned Completes and Man
8/11/2022 10:51:28 PM
Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
8/11/2022 4:14:19 AM
Responsibilities include, but are not limited to: 1. Trial and site administration: Track (eg essential documents) and report Ensure collation and distribution of study tools and documents 2. Document management: Prepare documents and correspondence Collate, distribute/ship, and archive clinical documents, eg eTMF Assist with eTMF reconciliation Execute eTMF Quality Control Plan 3. Site Start-Up responsibilities: Collaborate with other country roles to: In a timely manner, provide to and collect
8/11/2022 4:09:38 AM
8/11/2022 2:11:59 AM
TIME: Work with project team to set up and maintain project schedule. Update timelines within MS Project, CTMS, project governance tool, and other trackers. Escalate when timelines are at risk COST: Work with Project Lead to assist with TAQ/TAR (timesheet vs budget) reviews; vendor financial tracking & reconciliation; sponsor contract financial tracking & reconciliation; and final project financial reconciliation SCOPE: Work with Project Lead to conduct Contract vs Study Plan Review. Maintain tra
8/11/2022 2:08:45 AM
8/11/2022 2:04:19 AM
8/11/2022 2:02:18 AM
Reporting to a People Analytics Manager, the position collaborates with a small, centralized, global team of Workforce Analysts to develop and deliver Workday reports. Able to leverage Workday and Workday products (eg, Prism) in building custom reports, advanced reports, and Matrix reports to be consumed by all levels of HR and business line Applies people data subject matter expertise and analytical insight to Talent Acquisition, Management, or Compensation-related projects and initiatives Creat
8/10/2022 10:36:42 PM
Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: entry of safety data onto adverse event database(s) and tracking systems review of adverse events for completeness, accuracy and appropriateness for expedited reporting write patient narratives code adverse events accurately using MedDRA determine expectedness/listedness against appropriate label identifies clinically signific
8/10/2022 10:33:21 PM
Clinical Research Associate I I. Essential Job Duties: 1) Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 2) Responsible for all aspects of site management as prescribed in the project plans 3) General On-Site Monitoring Responsibilities 4) Ensure the study staff who will conduct the protocol have received the
8/10/2022 8:45:46 PM