Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1537880 To be eligible for this position, you must reside in the same country where the job is located. Seeking _experienced_ candidates near major hub airports in the Southeast, Northeast, Central and West regions. Job Overview Perform monitoring and site management work to ensure that sites are conductin…

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Sr CRA (Level I) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial…

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Sr CRA (Level I) Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial…

Overland Park, KS, United States of America Carlsbad, CA, United States of America Full time R1570353 Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regula…

Overland Park, KS, United States of America Carlsbad, CA, United States of America Full time R1570353 Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regula…

Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1541452 Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: - Perform site monitoring visits (selection,…

Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1541452 Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: - Perform site monitoring visits (selection,…

Job Description A growing and exciting biotech company specializing in central nervous system (CNS) diseases are hiring for a Senior Clinical Research Associate (SCRA). The SCRA will be responsible for site management and monitoring activities at assigned sites across assigned programs ensuring the trial is conducted in compliance with the protocol, ICH/GCP, applicable regulatory requirements and applicable SOPs/Work Instructions. \n \n This role is fully remote, with approx. 70% travel expecte…

Fortvita Biologics is a biopharmaceutical company based in the San Francisco Bay Area specializing in antibody discovery and engineering, with platforms that span antibody-drug conjugates (ADCs), bispecifics, and multispecifics. Our pipeline targets oncology, immunology, and neurodegenerative diseases and is supported by a team of over 100 across research, development, regulatory, and operational functions. With a global clinical presence and an emphasis on thoughtful design and agile execution…

Carlsbad, CA, United States of America Sacramento, CA, United States of America San Francisco, CA, United States of America Full time R1554995 IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this posit…

Carlsbad, CA, United States of America Sacramento, CA, United States of America San Francisco, CA, United States of America Full time R1554995 IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this posit…

Carlsbad, CA, United States of America Sacramento, CA, United States of America San Francisco, CA, United States of America Full time R1554995 IQVIA is now hiring for a Senior Clinical Research Associate located on the West Coast, US to join our growing Early Clinical Development team working exclusively in Phase I. Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this posit…

About the Role: We are looking for a Clinical Research Associate to manage clinical trial activities from initiation to closeout. This role involves ensuring trials are conducted in compliance with regulatory standards, monitoring site activities, and ensuring data integrity. The ideal candidate is organized, detail-oriented, and experienced in managing complex clinical trials. Key Responsibilities: Monitor clinical trial sites to ensure protocol adherence and compliance with regulatory standar…

Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinical, Phase I through Phase IV, and post-marketing studies. Responsibilities Prepares and completes critical study documents and performs final editing/proofing prior to publishing (e.g. protocol; synopsis; flowchart; informed consent template; investigator brochure; monitoring guideline;…

Please note this is a limited-term position with an estimated duration of 12 months, with the possibility of extension. This position will require travel outside of WA state Clinical Research Associate II: Assist in the organization, implementation, and completion of clinical research studies in compliance with all applicable laws and regulations, institutional/ departmental guidelines, standards of Good Clinical Practice (GCP), and within budget. Create, collect, and review study-related docum…

Job Description The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and bi…

Clinical Research Associate II (CRA II) Kelly® Science & Clinical is seeking a Clinical Research Associate II for a six-month, full-time contract position with a large clinical research organization (possibility of extension/conversion). This remote, home-based position supports regional clinical studies across the Western U.S. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pa…

Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1566259 Role Overview: As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key Responsibilities: Site Visits: Conduct selection, initiation, monitoring, and close-out visi…

Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1566259 Role Overview: As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key Responsibilities: Site Visits: Conduct selection, initiation, monitoring, and close-out visi…

Overland Park, KS, United States of America Durham, North Carolina, United States of America Parsippany, New Jersey, United States of America Carlsbad, CA, United States of America Full time R1566259 Role Overview: As a Clinical Research Associate, you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research. Key Responsibilities: Site Visits: Conduct selection, initiation, monitoring, and close-out visi…