Clinical Researcher Jobs

This is a fully on-site position in Las Vegas, Nevada Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a co

The Kimberly and Eric J. Waldman Department of Dermatology at the Icahn School of Medicine at Mount Sinai is dedicated to delivering superior, comprehensive dermatologic care that exceeds patient expectations, and to advancing the science of dermatology through research and education. From preparing

This is a fully on-site position in Salt Lake City, Utah Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a

Location:Hematology Oncology of Indiana Pay Range:$24.83 - $46.12 Job Description Summary Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator III (RN) performs tasks independently, consistently and accuratel

This is a fully on-site position in Tempe, AZ Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborat

Unit: School of Medicine Department: Neurosurgery Department Summary: The VCU School of Medicine (SOM) is seeking candidates with an interest in clinical research to join the cross-departmental School of Medicine research group, the Clinical Trial Collaborative (CTC). This is a salaried, benefited p

Fortrea is recruiting! Fortrea in Paris is looking for a Senior Clinical Research Associate I (SCRA I) to be Sponsor-Dedicated. Key Responsibilities: Monitor Clinical Trials - conduct site visits to ensure compliance with protocols, regulatory requirements and Good Clinical Practice (GCP) - National

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities: Assure all study requirements are met and documented and meet

Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the Colorado, Nevada or Utah region. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). Co

Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in the Florida. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participa

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator (open rank) - LCPC / CPS Team Position #: 00678098 – Requisition #: 40341 Job Summary: Clinical Science Professionals at all levels perform clinical research related functions which

Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in Texas or Mid-West (Kansas, Missouri, Nebraska, Iowa, Colorado). WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgeme

LocationSAINT LOUIS, MO 63110

 Scheduled Hours40 Position SummaryClinical Research Coordinator for the Cardio-Oncology and Amyloid Research Center. Assists investigators as coordinator of a basic to moderately complex clinical research study with a focus on cardiac amyloidosis; may be respo

LocationSAINT LOUIS, MO 63110

 Scheduled Hours40 Position SummaryThis is an opportunity to join clinical research teams in the Division of Pulmonary and Critical Care Medicine. The position will be with the sarcoidosis group led by Adam Anderson, MD and the interstitial lung disease (ILD) g

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo

Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities fo

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Functio