About the Role The Senior Regulatory Start-Up Associate (Senior RSA) is responsible for the planning, preparation, coordination, and submission of country- and site-level regulatory and ethics applications during the start-up phase of clinical trials and, where applicable, throughout
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up
Kenvue is currently recruiting for a: HCP Marketing Manager What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house
Job Overview The Associate CPM Director will manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with
Base level role Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of e CRF completion guidelines, entry of test data for
IQVIA seeks an Associate CPM Director with strong CNS study leadership to manage operational delivery from pre-award to close-out. You will drive strategic leadership, oversee multicountry programs, and ensure quality, time, and budget targets. You will leverage
Professor/Associate professor (Professional Equivalent Specialist/Head Clinical Unit) and Head of Division: Health Systems and Public Health Department Description/Departement Beskrywing Faculty of Medicine and Health Sciences Department of Global Health Division of Health Systems and Public Health Professor/Associate professor (Professional
Senior Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the
Brief Description Brief Posting Description The Division of Clinical Psychology, in the Department of Psychiatry, invites suitably qualified Joint staff, interested in being part of a dynamic, growing academic division, to apply for this Academic Headship. This
IQVIA Argentina is seeking an Associate Centralized Monitor in Bloemfontein, South Africa. This full-time role involves providing project support, administrative assistance, and monitoring site performance throughout clinical studies. The ideal candidate will possess a B. Sc. degree in Life
NORTH-WEST UNIVERSITY (MAHIKENG CAMPUS) FACULTY OF HEALTH SCIENCES SCHOOL OF NURSING POSITION NUMBER: M VACANCY: PROFESSOR/ASSOCIATE PROFESSOR PEROMNES: A5/A6 EMPLOYMENT TYPE: PERMANENT APPOINTMENT NOTE: Those who have previously applied need not to re-apply as the university has
NORTH-WEST UNIVERSITY (MAHIKENG CAMPUS) FACULTY OF HEALTH SCIENCES SCHOOL OF NURSING VACANCY: PROFESSOR/ ASSOCIATE PROFESSOR/ SENIOR LECTURER POSITION NUMBER: M PEROMNES: A5/A6/A7 EMPLOYMENT TYPE: PERMANENT APPOINTMENT NOTE: THOSE WHO HAVE PREVIOUSLY APPLIED NEED NOT TO RE-APPLY AS
NORTH-WEST UNIVERSITY (MAHIKENG CAMPUS) FACULTY OF HEALTH SCIENCES SCHOOL OF NURSING VACANCY: PROFESSOR/ ASSOCIATE PROFESSOR/ SENIOR LECTURER POSITION NUMBER: M PEROMNES: A5/A6/A7 EMPLOYMENT TYPE: PERMANENT APPOINTMENT NOTE: THOSE WHO HAVE PREVIOUSLY APPLIED NEED NOT TO RE-APPLY AS
Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.
We are seeking an experienced and strategic Digital Health Senior Associate to join our Health Practice. This senior role is designed for a professional who combines deep expertise in health information systems with the gravitas and communication
Job Overview Lead the execution of Centralized monitoring activities for multiple sites and studies from initiation through closeout, ensuring delivery of clinical study management and project deliverables on time in accordance with SOPs, policies, GCP, and regulatory requirements.
Job Overview Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and are in accordance with
Job Overview Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and is in accordance with
Job Overview Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics. Essential Functions Complete appropriate role-specific
IQVIA, located in Centurion, South Africa, is seeking a candidate to provide project-related assistance to assigned project teams. This role involves ensuring compliance with regulatory requirements, meeting quality metrics, and providing administrative support to the clinical study management team.