Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
A Senior Clinical Research Associate will work closely with clinical operations and the cross-functional study execution team to implement all aspects of clinical trials to support multiple clinical programs. Senior Clinical Research Associate. The position will liaise with clinical sites, central l...
The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Senior Clinical Research Associate - SPS (Stiff Person Syndrome) is a seasoned professional with wide-ranging study and site management experience and a thorough understanding of GCP and ICH principles. CRA will be assigned as the primary point of contact for several sites in collaborative partn...
Senior Clinical Research AssociateA Senior Clinical Research Associate will work closely with clinical operations and the cross-functional study execution team to implement all aspects of clinical trials to support multiple clinical programs. The position will liaise with clinical sites, central lab...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for...
A minimum of 12 months experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite). Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. ...
Senior Clinical Research Associate. We are partnered with a rapidly expanding Neurology company in their search for a Senior Clinical Research Associate. This organization has already received multiple approvals for therapies generating upwards of 100 million dollars in revenue per year and they hav...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
Job Title: Senior Research Associate, Drug Metabolism. The primary responsibility of this Biologics Bioanalytical Research Associate is to provide bioanalytical support to DMPK project representatives on biologics discovery teams. ...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...