Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate's degree with 7+ years' experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...
A company is looking for a Clinical Research Associate in Oncology. ...
Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor's degree in a cli...
A company is looking for a Senior Clinical Research Associate. Key Responsibilities:Conduct site monitoring visits in accordance with regulatory requirementsManage progress of assigned studies by tracking regulatory submissions and approvalsCreate and maintain documentation regarding site management...
The Clinical Research Associate I will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Clinical Research Coordinat...
The Clinical Research Associate I will function under the supervision of the Clinical Research Supervisor, coordinating and maintaining diverse activities related to clinical trials at the John Wayne Cancer Institute. Clinical research coordination, or 2 years of clinical research data entry or equi...
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 global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Asso...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
The Clinical Research Associate I will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Clinical Research Coordinat...
Previous experience as a Clinical Research Coordinator or similar role. Coordinate and oversee clinical research studies from start to finish. Knowledge of clinical development processes and compliance management systems. Familiarity with clinical laboratory procedures and data collection methods. ...
Minimum two (2) years of experience in clinical protocols involving research methodology/research study design, and hypothesis testing. May coordinate research project activities with other research study centers. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Min...
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. ...
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 will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor’s degree in a cli...
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...
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. ...
Bachelors degree with 4+ year experience as a Clinical Trials Associate; or Associate’s degree with 7+ years’ experience as a Clinical Trials Associate; or 10+ years clinical research experience. Participate in clinical research teams to ensure the most effective and efficient conduct of clinical re...
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 ...
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...
Part-timeMinimum Qualifications: - Bachelor's Degree preferred....
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...
Coordinate and oversee clinical research studies from start to finish. Clinical trial management, patient communications, document procurement. Management of clinical trial participants, assuring compliance with trial protocols. Adhere to Good Clinical Practice (GCP) guidelines. ...
The Clinical Research Data Associate III manages the data for assigned research studies. In addition, may supervise clinical research staff or clinical data managers, perform sophisticated statistical analysis, and work with bioinformatics to develop and maintain trial management and validation syst...
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...