Position Description Job Title: Senior Clinical Trial Manager Location: South Africa Reports to: Associate IAVI is seeking a highly motivated Senior Clinical Trial Manager (CTM) who will be responsible for the management operational activities for the conduct of clinical trials according to ICH/GCP guidelines and relevant regulatory operations of late phase and/or highly complex clinical trials, mentor other clinical operations staff, and lead senior management appropriately. Lead clinical trial team meetings and contribute clinical updates to
client is needing a fully bilingual bookkeeper to trial balance, living in the Stellenbosch area, to join system Debtors and Creditors functions Maintain the trial balance Account reconciliation to assert the accuracy
Services industry is looking for a Bookkeeper to Trial Balance in Goodwood.
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for a Bookkeeper to Trial Balance in Goodwood. Responsibilities: Bookkeeping to Trial Balance Debtors /
mission to disrupt patient recruitment for clinical trials (a $100 billion dollar sector) and connect market-ready treatments to the patients who need them. Clinical trials need millions of qualified patient volunteers but and are interested in participating in clinical trials. The successful candidate must be able to speak in clinical trials and conducting a basic medical screening Discussing available trials with patients screening to evaluate a patient's eligibility for a trial Transferring pre-qualified patients to clinics for
reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support projects. RESPONSIBILITIES - Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which customers. - Prepares and maintains core clinical trial submission dossiers in accordance with applicable Investigational Medicinal Product Dossier, clinical trial justifications with minimum support of senior staff
reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support - Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and Investigational Medicinal Product Dossier, clinical trial justifications - May strategically plan and perform
industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating timelines Not required, but experience with orphan drug designations and PSP/PIPs a plus Please consider
delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients) independently - Comprehensive understanding of clinical drug development process - Ability to establish and maintain
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