Clinical Trial Coordinator

Responsibilities include, but are not limited to: • Trial and site administration: o Track (e.g. essential documents) and report o Ensure collation and distribution of study tools and documents • Document management: o Prepare documents and correspondence o Collate, distribute/ship, and archive clinical documents, e.g. eTMF o Assist with eTMF...

Job DescriptionAt 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 science a step...

Performs Programming Support Tasks:Assists study project team leads with creating, executing, maintaining, and validating programs for data transfer and manipulation.Actively Seeks Information:Demonstrates a proactive approach to understanding the programming role and processes.Functions as a Team Member:Collaborates with study team leads to ensure task...

Senior Specialist, Clinical Data Management WDescriptionPosition Summary: Type of Role: This is a professional individual contributor role that provides oversight and accountability for more than one low to moderate complexity trial or one high complexity trial. May be a member of more than one project of low to moderate complexity or member of one project...

Senior Specialist, Clinical Data Management WDescriptionPosition Summary: Type of Role: This is a professional individual contributor role that provides oversight and accountability for more than one low to moderate complexity trial or one high complexity trial. May be a member of more than one project of low to moderate complexity or member of one project...

Education and Experience: •Major in Clinical Medicine, Pharmacy, Biology or Nursery, Master Degree or Above 临床医学、药学和生物等专业硕士及以上学历 •At least years clinical trial supervision experience, or at least years clinical study project management experience ...

Responsibilities / DutiesIn this position, you will manage clinical projects to ensure successful delivery of lab services in the Asia region, including kits shipment, sample testing, and sample management for a clinical studyAct as a liaison between Labcorp Central Lab Services (CLS) Global Study Manager and various CLS departments involved in the clinical...

We're looking for people who are determined to make life better for people around the world. This job is under Lilly China Drug Development and Medical Affair Center (LCDDMAC) for Diabetes, Obesity, and Metabolic area, one of the strategic therapeutic areas of Lilly China. The Clinical Research Physician will take core medical role as scientific leader in...

Job TitleAssociate Clinical Affairs ManagerJob DescriptionIn this role, you have the opportunity to· Provide Chinese clinical strategy for NPI; Lead the clinical plans development to be compliance with GCP, the regulation, Philips harmonized clinical SOPs;· Lead the clinical evaluation projects across the product lines, work closely with Regulatory team,...

JOB DESCRIPTION Job Title Associate Clinical Affairs Manager Job Description In this role, you have the opportunity to · Provide Chinese clinical strategy for NPI; Lead the clinical plans development to be compliance with GCP, the regulation, Philips harmonized clinical SOPs; · Lead the clinical evaluation projects across the product lines, work...

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers...

Job DescriptionMonitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to...

Job Summary: The Regional Study Coordinator (RSC) is responsible for the successful delivery of all operations of a clinical study in their specific area of the world. The RSC acts as the appointed Liaison between Global Project Management, Client Representatives and other LCLS departments involved in the clinical study to ensure the successful...

Job DescriptionResponsible for compliance with applicable Corporate and Divisional policies and procedures.Provide tactical and strategic oversight of clinical trials to ensure compliance across all TherapeuticAreas/ Clinical OperationsDevelop and assess cost, resource projections and metrics for the functionIntegral participant during regulatory inspections...

Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a crucial role in connecting evidence-based medical decision support with colleagues and stakeholders to enhance health and treatment outcomes. Whether you are establishing frameworks to ensure the scientific validity of our evidence, offering impartial and medically necessary...

Job DescriptionPurposeDescribe the primary goals, objectives or functions or outputs of this position.To enable AbbVie' s emergence as a world class R&D organization, the position plays a key role in ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies.ResponsibilitiesList up to 10 main...

Job DescriptionSummarized Purpose:Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Ensures that data will pass international quality...

Job DescriptionSummarized Purpose:Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Ensures that data will pass international quality...

Job TitleCT Clinical ScientistJob DescriptionJob title:CT clinical scientistKey Areas of ResponsibilityIdentify and connect new customer needs, solutions and technologies to initiate new methods (or disruptive enabling technologies) of diagnosis, treatment and/or care within domainInitiate and drive co‐creation and discovery in line with overall strategy...

Manages all clinical operational and quality aspects of allocated studies in compliance with ICH GCP. Takes ownership for achieving the final clinical deliverable within the contractual time period specified within PPD development's contract with the customer. Manages CRF collection and query resolution process and assists as needed. Develops clinical...