At IQVIA, we are advancing healthcare by accelerating the development of innovative therapies that improve patient outcomes worldwide. As a global leader in clinical research, healthcare intelligence, and data science, we empower our people to solve
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Updated: Today Location: Bloemfontein, EC, South Africa Job ID: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management and
# Quality Review SpecialistApplylocations: Bloemfontein, South Africa: Bellville, South Africa: Centurion, South Africatime type: Full timeposted on: Posted Todayjob requisition id: R Internal Job Description PURPOSE Quality Reviewer RESPONSIBILITIES Conduct internal Data Management Quality Reviews in
1 - 2 years experience in Personal and Business Banking. Previous experience in branch banking or contact centre environment with good understanding of bank processes, policies and products. Duties and Responsibilities: Engages with customers in order
# Global Study Manager - Single Sponsor dedicated (in EMEA)Applylocations: Warsaw, Poland: Porto Salvo, Portugal: Budapest, Hungary: Bloemfontein, South Africa: Prague, Czech Republictime type: Full timeposted on: Posted Todayjob requisition id: R Job Overview The Global
Lead CRA (Sr CRA II) – Location: Bloemfontein, South Africa Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practices (GPP)
Role Overview In this senior leadership role, you will provide strategic direction and operational oversight to Clinical Project Management teams, ensuring projects are delivered on time, within budget, and to the highest quality standards. You will
Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgement and experience to evaluate overall