A clinical trial management system (CTMS) is a software system used to manage clinical trials in clinical research. This CTMS will serve as a single, centralized, web-based enterprise resource to support clinical research studies conducted within or across the three institutions.
Create a Job Alert for Clinical Trial Management System Jobs
Create a Job Alert
Get notified when new Clinical Trial Management System jobs are posted
Overview. Job Summary. The research coordinator II is responsible for coordinating the conduct of research protocols. with general supervision. assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes recruitment, screening, enrollment, randomiz...
We are seeking an experienced Clinical Research Associate (CRA) to monitor clinical trials for device studies. The successful candidate will be responsible for ensuring compliance with regulatory requirements, good clinical practice (GCP), and company standard operating procedures (SOPs). This is an excellent opportunity to join a dynamic team. Key Responsibilities. Conduct site qualification visits, site initiation visits, interim monitoring vis...
We are seeking an experienced Clinical Research Associate (CRA) to monitor clinical trials for device studies. The successful candidate will be responsible for ensuring compliance with regulatory requirements, good clinical practice (GCP), and company standard operating procedures (SOPs). This is an excellent opportunity to join a dynamic team. Key Responsibilities. Conduct site qualification visits, site initiation visits, interim monitoring vis...
Description. Support study start-up, maintenance, and close-out activities across multiple clinical trials. Coordinate with CROs, clinical sites, and vendors to ensure timely delivery of study milestones. Track and manage clinical supplies, shipments, and site communications. Assist in the development and review of study-related documents (e.g., protocols, ICFs, CRFs, monitoring plans). Support data collection and query resolution. Participate in...
Job Title: Clinical Trial Associate. Location: Plainsboro , New Jersey. Type: Contract - 6 month renewable. Contractor Work Model: Hybrid - Plainsboro, NJ. Leading Pharmaceutical Company located in NJ is hiring a. Clinical Trial Associate w/. 5 years industry experience. If you want to be a part of this groundbreaking work, please apply. . Job Description. The Clinical Trial Associate will support Clinical Trial Managers and Clinical Trial Teams...
Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for ICON Clinical Research. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any inf...
About This RoleRDI is seeking a detail-oriented and motivated Senior Clinical Research Associate (CRA) to join our dynamic team. In this role, you will act as a critical link between the clinical sites and our research teams, ensuring that all clinical trials are conducted according to regulatory guidelines, protocols, and ethical standards. You will have the opportunity to work closely with investigators and other health professionals to monitor...
About This Role. RDI is seeking a detail-oriented and motivated. Senior Clinical Research Associate (CRA). to join our dynamic team. In this role, you will act as a critical link between the clinical sites and our research teams, ensuring that all clinical trials are conducted according to regulatory guidelines, protocols, and ethical standards. You will have the opportunity to work closely with investigators and other health professionals to mon...
About This Role. RDI is seeking a detail-oriented and motivated Senior Clinical Research Associate (CRA) to join our dynamic team. In this role, you will act as a critical link between the clinical sites and our research teams, ensuring that all clinical trials are conducted according to regulatory guidelines, protocols, and ethical standards. You will have the opportunity to work closely with investigators and other health professionals to monit...
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundatio...
Job Title. Senior. Clinical Trial Manager. Job Description. Join our dynamic team as a. Senior. Clinical Trial Manager where you will play a pivotal role in leading, overseeing, planning, and executing assigned clinical studies. Collaborate closely with the Clinical Program Manager and other departments to ensure the successful delivery of key project milestones. Responsibilities. Collaborate with the Clinical Program Manager to lead and oversee ...