Expected Travel: Up to 25% Requisition ID: 14214 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
The Team The Outpatient Departments across the Northwest supports multiple specialities. We offer general medical, surgical, gynaecology, orthopaedic, respiratory, paediatric, stomal therapy, cardiology, cardiac rehab, neurology, neurosurgical, dermatology, endocrinology, infectious diseases, gastroenterology, nephrology, staff health and
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs,
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a
The Team Our Emergency Departments at Mersey Community Hospital (MCH) and North West Regional Hospital (NWRH) deliver high-quality emergency care to communities across North-West Tasmania. Each site has its own identity, leadership, and patient flow, whilst
The Team The Close Observation Unit (COU) at the Mersey Community Hospital is a six‑bed level 2 critical care area designed for acutely ill medical and surgical patients who require close haemodynamic, cardiac, respiratory, or neurological
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,
6-Month Fixed-Term Contract About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support
Project Specialist-Firecrest ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
We provide meaningful careers that connect people with purpose. We are united by a common purpose of providing the best and safest care; and by our shared values of Care, Truth, Participation, Compassion and Dignity. Netcare
The application closing date:12 Sept 2026 Description: The purpose of this position is to support implementation of a community-based HIV prevention for men attending taverns in rural KwaZulu-Natal. The professional research nurse will deliver nurse-led mobile
Senior Site Activation Specialist, ICF Lead Location: South Africa, Slovakia, Serbia, Bulgaria Work Model: Hybrid or Homebased Job Overview The Senior Site Activation Specialist, ICF Lead performs country-level Site Activation (SA) activities in compliance with applicable
(Senior) Clinical Project Manager - Global Study Leadership Centurion, South Africa | Full time | Home-based | R I like that were different. I like that were a unique organization unlike any other. I like to think of us
At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. Youll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the
IQVIA Biotech seeks a Clinical Trial Manager to lead multi-regional trials, ensuring delivery in line with GCP/ICH and SOPs. You will coordinate clinical teams, manage risks and finances, and collaborate with stakeholders to meet recruitment targets and milestones. Based
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across
Select how often (in days) to receive an alert: Create Alert Shape the future of clinical trial readiness across multiple markets – and help life-changing treatments reach patients faster. Your new role As the Study Start-Up (SSU) Manager, you
Job Description Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we
ATS Client in Pretoria is seeking a Clinical Data Manager to oversee data collection, validation and QC across clinical studies. You will design e CRF layouts, DMPs and test EDC databases, ensuring accurate data capture and timely archiving. Strong English