Clinical Study Team Assistant I, Fsp
hace 4 semanas
**Primary Responsibilities**:- Provides study level operational support to the Core Study Team from study start up to close out and submission with general direction:- Management and oversight of Study Team shared spaces- TMF maintenance, compliance, and oversight- Analyze, interpret, and follow up on metrics- Management and oversight of Study Management Platform- Analyze, interpret, and follow up on metrics- Registry and/or Clinical Trial Management system(s) compliance and maintenance- Tracking and oversight of study level information; follow up with functional lines as needed- Liaising with cross functional study team members:- Provide study level reporting to support management of clinical trial data, clinical trial budget and timelines- Quality Control (QC) of essential clinical trial, Clinical Study Report (CSR) and regulatory submission documentation- Manages engagement of Independent Oversight Committees- Provides support to the CSTL and Clinical Quality Lead with Inspection Readiness Activities- Assists the CSTL with oversight and tracking of Clinical Trial Budget spend- Provides logístical/operational support to Study Management for Investigator Meetings- Provides status updates on key tasks and activities to the CSTL and contribute to the Core Study Team Meetings as an active Core Study Team member- Works proactively with mínimal oversight to coordinate and prioritize multiple key study tasks in support of clinical trial systems and processes- Uses established procedures and methodologies to ensure the completion of assigned tasks according to timelines and to required quality standards- On occasion, supports short term Clinical Operations Special Project requests (e.g. workstreams, initiatives, projects)- Manages conflicting priorities to ensure excellent support to assigned study teams with general direction- Manages own time to meet agreed targets; develops plans for short-term work activities on own projects (timelines, work plans, deliverables)- Completes training assigned by Client and/or Parexel FSP, as necessary, including general training requirements, SOPs, system, and process related training.- Adheres to EP and Client SOPs and processes**Education and Certification**:- Bachelor’s Degree (B.S or B.A) with 0 to 3 years’ experience or Master’s Degree (M.S, M.A or M.B.A) with 0 to 1 years’ experienceLI-REMOTE
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Clinical Study Team Assistant I
hace 3 semanas
Desde casa, México Parexel A tiempo completoThe Clinical Study Team Assistant I (CSTA I) is an essential part of the study team and is responsible for supporting key clinical trial tasks for assigned studies to ensure compliance with timelines, Good Clinical Practice (GCP), and client Standard Operating Procedures (SOPs). The role collaborates with global study team members and is responsible for...
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Clinical Study Team Assistant I, Fsp
hace 2 semanas
Desde casa, México Parexel A tiempo completoJob Description Provides study level operational support to the Core Study Team from study start up to close out and submission with general direction: - Management and oversight of Study Team shared spaces - TMF maintenance, compliance, and oversight - Analyze, interpret, and follow up on metrics - Management and oversight of Study Management Platform -...
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Clinical Study Team Assistant I
hace 2 semanas
Desde casa, México Parexel A tiempo completoProvides study level operational support to the Core Study Team from study start up to close out and submission with general direction: - Management and oversight of Study Team shared spaces - TMF maintenance, compliance, and oversight - Analyze, interpret, and follow up on metrics - Management and oversight of Study Management Platform - Analyze,...
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Clinical Study Team Assistant I
hace 1 semana
Desde casa, México Parexel A tiempo completoProvides study level operational support to the Core Study Team from study start up to close out and submission with general direction:- Management and oversight of Study Team shared spaces- TMF maintenance, compliance, and oversight- Analyze, interpret, and follow up on metrics- Management and oversight of Study Management Platform- Analyze, interpret, and...
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Senior Study Manager
hace 3 semanas
Desde casa, México Parexel A tiempo completo**Senior Study Manager****Position Purpose**:- The Senior Study Manager (SSM) has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies- The SSM leads and manages the tactical execution of one or more clinical studies from study startup through database release and...
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Senior Clinical Research Associate I
hace 3 semanas
Desde casa, México Parexel A tiempo completo**Parexel FSP is looking for multiple Sr CRAs in Mexico!**The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and...
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Clinical Operation Assistant
hace 2 semanas
Desde casa, México Parexel A tiempo completoAs a Clinical Operations Assistant (COA) you will provide administrative support to various project team members. Your daily tasks will vary including site payments, management of site supplies, trial master file related tasks, and limited site facing tasks to support the efficiency, accuracy, and quality of the trials. Study Site Experience and strong...
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Clinical Study Planning Senior Associate Manager
hace 4 semanas
Desde casa, México Parexel A tiempo completoExternal Job Description**Responsibilities**:- Lead the development of realistic study timelines, from design through final study reporting on priority programs- Maintaining accuracy of clinical study timeline information in Company data control systems (e.g., Planisware (PPM)- Tracking, documenting, and ensuring key stakeholder involvement and timely...
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Site Activation Partner I
hace 2 semanas
Desde casa, México Parexel A tiempo completoThe Site Activation Partner I (SAP I) is responsible for leading or supporting operational activities from start up to close out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and client standards. Responsibility within a country and may span over more...
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Site Activation Partner
hace 3 semanas
Desde casa, México Parexel A tiempo completoResponsible for supporting the SRPs and investigator for Targeted Sites:**Clinical Trial Site Activation & Conduct**- Assist with study site activation activities to ensure timely site activation- Register investigator sites in Client registries, as required- Support and/or coordinate central Investigator Review Board (IRB) submissions when needed.- Work...