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...
A bit about us:Our client is a contract research organization, a type of organization that plays a vital role in the development of new treatments and medications for patients. They specialize in a variety of therapeutic areas including Transplants, Oncology, Rare Disease & Cell & Gene Therapy.Why j...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Position SummaryThis position reports to the SVP Global Business Operations, and collaborates with the Chief Information Officer (CIO), as well as clinical executive leaders. The Executive Director, CTMS & eTMF will create strategic and transitional plans to support effective clinical trial manageme...
Established CRO seeks experienced BiostatisticiansThis Jobot Job is hosted by: Hunter PraterAre you a fit? Easy Apply now by clicking the "Apply on company site" button and sending us your resume.A bit about us:Our client is a contract research organization, a type of organization that plays a vital...
Established CRO seeks experienced BiostatisticiansThis Jobot Job is hosted by: Hunter PraterAre you a fit? Easy Apply now by clicking the "Apply on company site" button and sending us your resume.A bit about us:Our client is a contract research organization, a type of organization that plays a vital...
We are a team of clinical trial experts who are dedicated to the success of our clients so that patients can receive much-needed treatments. From the beginning, we have nurtured a culture where patients’ needs and the needs of our valued clients come first, where the quality of our work is the best,...
Job Overview: Labcorp Drug Development has an exciting opportunity for an Associate Clinical Data Manager within the Clinical Data Management team. The Associate Clinical Data Manager can be remotely located anywhere within the United States or Canada. Collaborate and functionally report to Lead DM ...
Job Overview: Labcorp Drug Development has an exciting opportunity for an Associate Clinical Data Manager within the Clinical Data Management team. The Associate Clinical Data Manager can be remotely located anywhere within the United States. Collaborate and functionally report to Lead DM (LD...
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the...
Description Position at Premier Research Premier Research helps highly innovative bio-pharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, ra...
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the ...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world's largest pharmaceutical companies to emerging biotechs. Veeva's software helps our customers bring me...
Job Description Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every c...
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 ...
Position Summary: The Clinical Systems Specialist is responsible for supporting the lifecycle management of clinical systems for Global Development Operations. This position will provide support for clinical systems, such as eTMF, Clinical Trial Management System (CTMS), Interactive Response Tec...
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...
$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...
*Clinical Research Associate - France, Remote**Who We Are* Synteract ® , a Syneos Health ® company, is a leading full service Contract Research Organization (CRO) with a successful three-decade track record of supporting emerging biotech and pharmaceutical companies. We provide customized Phase I th...
Veeva [NYSE: VEEV] is the leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, our customers range from the world’s largest pharmaceutical companies to emerging biotechs. Veeva’s software helps our customers bring me...
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the...
*The Role*Veeva Vault Clinical Data Management System (CDMS) is changing the way clinical data is managed in the industry. Vault CDMS combines Electronic Data Capture (EDC), coding, data cleaning and reporting into one application. Gone are the days of complex integrations that limit clinical data a...
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...
The Role Veeva Vault Clinical Data Management System (CDMS) is changing the way clinical data is managed in the industry. Vault CDMS combines EDC, coding, data cleaning, and reporting into one application. Gone are the days of complex integrations that limit clinical data availability, now resea...
*The Role*Veeva Vault Clinical Data Management System (CDMS) is changing the way clinical data is managed in the industry. Vault CDMS combines EDC, coding, data cleaning, and reporting into one application. Gone are the days of complex integrations that limit clinical data availability, now research...