A company is looking for a Clinical Research Regulatory Specialist. ...
IRB committee submissions with follow through to ensure successful outcome; scheduling, planning, and organizing start-up meetings and study site initiation meetings for clinical trials as directed by the PI or manager; tracking and completing case report forms and set up systems whereby forms are c...
The Stepdown ICU RN position is a full-time night shift role (7pm-7am) with a $20,000 sign-on bonus.Requires a BSN, SC RN license, and at least 2 years of relevant experience within the past 5 years.Key duties include overseeing shift operations, delegating care, supporting staff, and collaborating ...
A company is looking for a Clinical Research Coordinator I in Surgical Sciences. ...
A company is looking for a Clinical Research Coordinator I in Radiation Oncology. ...
A company is looking for a Project Coordinator I for Marketing. ...
A company is looking for a Clinical Research Assistant I. ...
A company is looking for a Project Coordinator, Marketing Operations. ...
A company is looking for a Part Time Clinical Administrative Coordinator. ...
A company is looking for a Clinical Coordinator. ...
A company is looking for a Construction Project Coordinator to support their team remotely. ...
A company is looking for a Clinical Research Regulatory Specialist. ...
A company is looking for an Information Technology Project Manager to drive complex labeling projects from initiation to completion. ...
A company is looking for a Part-Time Student Research Assistant. ...
A company is looking for an Operations Project Manager to oversee project management within service level agreements. Key ResponsibilitiesAct as the point of contact for project team members and manage project needsLead project meetings and monitor progress, keeping stakeholders informedEstablish an...
A company is looking for a Research Associate in Nuclear Medicine. ...
Clinical Nurse Coordinator RN Emergency Room. The Clinical Nurse Coordinator (CNC) ensures and delivers high quality, patient-centered care and coordination of all functions in the unit/department during the designated shift. In collaboration with other members of the management team, the CNC direct...
Do you want to join an organization that invests in you as a(an) Clinical Support Coordinator RN? At Summerville Medical Center, you come first. We are looking for a dedicated Clinical Support Coordinator RN like you to be a part of our team. The Clinical Support Coordinator RN supports high quality...
Project Manager Key Responsibilities:. Qualifications for Drywall Project Manager:. Coordinate with subcontractors, suppliers, and internal teams to ensure projects goals are met. Resolve issues and challenges that arise during the project lifecycle. ...
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Registered Nurse/Clinical Research Coordinator. Deeply rooted in community oncology centers globally, The START Center for Cancer Research ...
A clinical research coordinator will work on studies designed to measure the effectiveness of a drug, medical device, or process on the human body. The Research Coordinator works directly with Trial Sponsors, CRAs, and other Medical staff. Work responsibilities can include coordinating a clinic...
The coordinator works directly with the events team and assists in the production of weekly podcast. Experience coordinating events and projects. ...
The Project Manager provides dedicated, cross-functional project management of operational activities that supports the product lifecycle within the manufacturing site (e. The Project Manager is responsible for supporting regular and routine performance management and business reviews. The Project M...
Selectek has an immediate need to hire a Manufacturing Project Manager for a full-time position in the Spartanburg, South Carolina area. Interface with applicable managers in reviewing and evaluating project requirements and schedules. Prepare project schedules and checklists. Follows up with client...
In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. At least 2-3 years of Clinical Research Associate experience in the Cli...