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...
Minimum of 5+ years in clinical research industry. FDA, EMA), and clinical trial processes. Lead and manage multiple clinical trials from initiation to close-out, ensuring adherence to study protocols, timelines, and budgets. Conduct site visits to monitor study progress, evaluate data quality, and ...
We are seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies. The Division of Immunology and Rheumatology at Stanford University has a longstanding tradition of excellence in patient care, and is among the leading groups in the School of ...
Minimum of 4+ years in the clinical research industry. Combination of office work and travel to clinical sites, which may include healthcare environments and other clinical settings. Proven track record in managing clinical trials and site monitoring. In-depth knowledge of clinical trial processes, ...
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. The Mormino Laboratory within the Department of Neurology and Neurological Sciences is seeking a Clinical Research Coordinator Associate (CRCA) to work on studies that use positron e...
Your main responsibilities as a Clinical Research Associate II: Support study team with clinical trial management activities including protocol review, da Clinical Research, Research Associate, Clinical, Associate, Research, Healthcare, Staffing. R&D Partners is seeking to hire a Clinical Research A...
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. To further this mission, the department is seeking a dedicated Clinical Research Coordinator Associate (CRCA) to oversee clinical studies within the Spine division. Clinical Research...
The candidate will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, contribute to clinical study reports, or...
Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives...
The Research Associate II works primarily in the laboratory to conduct relevant experiments and complex tasks under minimal supervision of other senior research associates or scientists. Research Associate II (Clinical NGS and RHT). Job Title: Research Associate II (Clinical NGS and RHT). The Resear...
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 ...
Clinical Research Associate II. Clinical Research Associate II. Clinical Research Associate II. Bachelor's degree in Life Sciences with 3-5 years of clinical research experience with a Sponsor company. ...
Clinical Research Associate who will be a vital role in the Clinical Operations Team. Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training 2 years of prior experience as a Clinical Research Associate preferre...
The candidate will be required to work closely with clinical study managers, clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, contribute to clinical study reports, or...
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...
As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and th...
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. ...
The Lead Clinical Research Associate (LCRA) is responsible for managing the development, coordination and implementation of site management and clinical monitoring responsibilities for clinical studies with guidance from the Clinical Trial Manager. Manages Regional Clinical Research Associates (CRAs...
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. ...
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...
Additional responsibilities: Provides technical assistance to study sites regarding the conduct of clinical research Track data report forms, reports, and documents necessary for completion of clinical study, both in-house and from participating study sites Oversees delivery and shipment of aligners...
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...