Clinical Researcher Jobs

Our Phase I team is currently seeking a Senior Clinical Research Associate with 3+ years of experience. Ideal candidates would have phase I experience and reside in the U.S. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for partic

DepartmentBSD MED - Emergency Medicine - Del Rios Research Staff About the DepartmentThe Del Rios lab, housed within the section of Emergency Medicine, centers on identifying and mitigating place-based barriers to preventing and surviving catastrophic medical emergencies. We partner with multidiscip

DepartmentBSD MED - Emergency Medicine - Beiser Research Staff About the DepartmentIn existence for over thirty years, the Section of Emergency Medicine is comprised of 27 full–time and 14 part-time faculty members, as well as an outstanding staff of research, administrative and clinical personnel w

Location:Genesis Cancer and Blood Institute Pay Range:$53,040.00 - $93,267.20 Position Summary The Clinical Research Coordinator functions as an integral part of the Research Team in clinical trial management at Oncology Consultants. The Clinical Research Coordinator is involved in multiple aspects

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet. The University of Miami/UHealt

Job OverviewPerform monitoring and site management work for a variety of protocols, site and therapeutic areas. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e.,

LocationST. LOUIS, MO 63108

 Scheduled Hours40 Position SummaryThis position seeks a highly organized coordinator to refer and track research participant study visits for the Memory and Aging Project (MAP) within the Knight Alzheimer Disease Research Center. Assists investigators as a coord

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

Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and procedures. Mentors, trains and reviews the work of less experienced clinical research staff. Oversees the clinical assessments

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of

Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking an Clinical Research Coordinator, to interact directly with our healthy volunteer participants while learning to read clinical research prot

DepartmentBSD MED - Rheumatology - Reid Research Staff About the DepartmentThe Section of Rheumatology has a proud and long tradition of excellence in research-based patient care and clinical discovery. The section is comprised of nationally and internationally known faculty with expertise in all ma

Work where every moment matters. Every day, more than 40,000 Hartford HealthCare colleagues come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network. Hartford Hospital is one of

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

University of Colorado Anschutz Department: Psychiatry Job Title: Clinical Research Coordinator Position #:00853222 – Requisition #: 41088 Job Summary: The Department of Psychiatry is seeking applicants for a full time (1.0 FTE) Clinical Research Coordinator (Research Services Clinical Science Profe

Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of

Job OverviewPerform 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, init

Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered.Job Overv

Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of