SUMMARY: The Manager, TMF Operations is responsible for the processing, maintaining and archiving of all essential documents in compliance with the relevant Standard Operating Procedures, country regulations and industry best practice. The Manager will assist to guide the strategy and lead the...
Job DescriptionLeading global quality process improvement and providing oversight and control of quality and compliance activities for 3,000+ global Trial Monitoring associates The Sr. PCM is accountable for leading global quality process improvement and compliance activities and for oversight and ...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
Manager or Assistant Director of Records Management (eTMF) provides expertise, oversight, implementation of systems and process improvement and training related to the trial master file (TMF) and eTMF systems, and other clinical trial documentation. The incumbent will ensure GCP compliance and inspe...
*Clinical Trial Manager - Major Sponsor **Remote *Kelly is currently seeking a Local Clinical Trial Manager for a long-term engagement at one of our Global clients.This role is a full-time, offering our enhanced benefit package options. As a Kelly employee within this group, you will be eligible for...
About this job Description Do you thrive on working on the cutting edge? Want to work with Event Driven, real time data, Interoperability on various Cloud platforms? Do you want to transform an industry? Crave for new challenges and solving problems using the latest in software technology...
About this job Description Do you thrive on working on the cutting edge? Want to work with Event Driven, real time data, Interoperability on various Cloud platforms? Do you want to transform an industry? Crave for new challenges and solving problems using the latest in software technology...
Overview ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our p...
Clinical Trial Manager needed in Ridgefield, CT for an American research-driven pharmaceutical company that strives to improve health of people and animals everywhere in the world. If you meet the requirements, please apply to this job. (Job#326617) 1 year w2 contract Pay rate: $70 - $74/hour ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Companys clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator s...
Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progress of the investigator ...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional C...
Remote Clinical Research Associate Location Austin, TX Type Direct Hire Salary $1 - $2 / yr ID BN38-2698383 Posted Aug 18, 2021 Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitor...
About HealthiVibe HealthiVibe improves the way clinical trials and patient-focused programs are conducted simplifying the study development and coordination process for pharmaceutical companies and enhancing the patient experience for participants in innovative ways. Our unique approach melds our te...
About HealthiVibe HealthiVibe improves the way clinical trials and patient-focused programs are conducted simplifying the study development and coordination process for pharmaceutical companies and enhancing the patient experience for participants in innovative ways. Our unique approach melds our te...
Careers that Change Lives In this exciting role as a member of Corporate Clinical Quality & Compliance, the Senior Clinical Quality Specialist (CQS) will be responsible for completing audits and ensuring that clinical personnel across Medtronic are operating within U.S. and international regulator...
$1 to $2 Per Year Based remotely, and reporting to the Director, Clinical Trials, the Site Manager/Clinical Research Associate (SM/CRA) is responsible for all site management and monitoring activities for Company’s clinical trials. As a SM/CRA, you are expected to oversee and manage the progre...
One of the *biggest global Biotechs* is looking to expand their management team.This is a position with a fast growing organization that is partnered with emerging companies on innovative trials. *BENEFITS** Internal progression* Very competitive salary package* Strong training and development suppo...
DescriptionJoin a talented team of Engineers to help create breakthrough ITOps and AIOps software in the era of cloud, micro-services, serverless and virtualization. We are seeking individuals with knowledge in Systems Management and/or Systems Monitoring Software and/or Performance Management Softw...
Kforce has a client in Middleboro, MA that is seeking a Data Platform Engineering Lead for a remote role. Summary:We are looking for a highly technical, hands-on developer who is also an effective people manager to build and own BI platforms across the cooperative and to drive democratization of dat...
TEAM: Clinical Development Operations Who We AreWe're a new kind of biotech, one with a bold mission to bring innovative new medicines at dramatically lower costs.What You’ll DoThe Trial Initiation Manager covers all aspects related to Site Initiation. You will develop a Site Initiation Management P...
Role: Resource needed to own multiple QA System activities (Change Control, QE/CAPA, Product Complaints, etc.) during reconfiguration/re-engineering of Quality Systems as well as continuous improvement activities. Will be getting own laptop. POSITION SUMMARY: This position is responsible for m...
Description Position at Premier Research Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases. We’re looking for an exceptional P...
SUMMARY: The Senior Specialist, Regulatory Affairs provides project representation and input to projects awarded to WCT for all stages of the drug development cycle. RESPONSIBILITIES: Liaise with the Regulatory Affairs Manager/Regulatory Affairs Director to plan, organise, compile progres...
This role will be responsible for the investigation of IT Enterprise related deviations to determine root cause and applicable corrective and preventive actions in accordance with FDA, MHRA, and other applicable global health authority regulations. Collaborate with IT and Quality resources to collec...
This role will be responsible for the investigation of IT Enterprise related deviations to determine root cause and applicable corrective and preventive actions in accordance with FDA, MHRA, and other applicable global health authority regulations. Collaborate with IT and Quality resources to collec...
Job Description Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
Job Description Subject to applicable law, all prospective hires will be required to demonstrate that they have been fully vaccinated for COVID-19 or intend to be vaccinated for COVID-19 by November 1, 2021, or qualify for a medical or religious accommodation to this vaccination requirement. Hir...
Senior Manager, Clinical Data Management - Permanent - Remote Proclinical Staffing is seeking a Senior Manager, Clinical Data Management to join a cutting-edge biotech company. This is a permanent role with the opportunity to work remotely. Primary Responsibilities As the Senior Manager, Clinical D...
Senior Manager, Clinical Data Management - Permanent - Remote Proclinical Staffing is seeking a Senior Manager, Clinical Data Management to join a cutting-edge biotech company. This is a permanent role with the opportunity to work remotely. Primary Responsibilities As the Senior Manager, Clinical D...
Senior Manager, Clinical Data Management - Permanent - Remote Proclinical Staffing is seeking a Senior Manager, Clinical Data Management to join a cutting-edge biotech company. This is a permanent role with the opportunity to work remotely. Primary Responsibilities As the Senior Manager, Clinical D...