Years of Experience: Typically requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead CRA role. Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, & company SOPs. ...
The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Additionally, this role will be responsible for implementing and monit...
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...
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...
This is a high travelling, on-site monitoring contract Clinical Research Associate opportunity for a West-Coast based Contractor. Add to the development of clinical protocols and relevant clinical forms. ...
If you are an experienced regional CRA looking to join a global leader in clinical research with a reputable sponsor aligned program, this is a good time to apply with ICON PLC. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for ...
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 Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
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. ...
As a Clinical Research Associate focused on medical devices, you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure that studies are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP), and company policies. Assist i...
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...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
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 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 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...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum...
Job Title: Senior Clinical Research Associate. We are seeking a highly experienced Senior Clinical Research Associate (CRA) to join our dynamic team. The ideal candidate will have a strong background in clinical research, with a focus on monitoring and ensuring the integrity of our clinical trials. ...
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...
Experience performing clinical research duties in a clinical research environment. Experience performing clinical research duties in a clinical research environment. Clinical Research Coordinator Assistant - TP132384. TES is currently hiring for a Clinical Research Coordinator Assistant. ...
Under supervision, the Research Assistant will assist in performing a number of duties for research studies focusing on mental illness, sleep, and successful aging. Under supervision, the Research Assistant will assist in performing a number of duties for research studies focusing on mental illness,...
The Assistant Clinical Research Coordinator will be assigned to assist in coordinating industry-sponsored and PI-initiated research studies involving human subjects that are being conducted in the MASLD research center. Under supervision, duties will include but not limited to: interpreting research...
Coral Research Assistant - 132659. Under supervision, the Coral Research Assistant will conduct various coral ecophysiological and engineering experiments, including data analysis, animal husbandry, aquarium maintenance, and the upkeep of algal and bacterial cultures. Coral Research Assistant - 1326...
The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI; Dr. Fortuna), the Center Research Supervisor, and/or the Cen...
The Clinical Research Coordinator will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and coordinator operational efforts. Demonstrated experience performing clinical research duties in a clinical research e...
Flatiron's NorCal District is looking for a Senior Project Manager for our Upper San Leandro WWTP project in San Leandro, CA. Manages all aspects of the project, including construction, budget and cash management for a single assigned project to ensure compliance with the project contract and owner ...