Job OverviewPerform 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 (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master Fil...
Job OverviewReview & approve investigations, Root Cause Analysis (RCA), Corrective and Preventive Action (CAPA) and Effectiveness Check (EC) plans and track till closure for medium/high-risk/complex quality events arising from Quality Issues, Audits, Inspections or during similar QA activities. Perform Quality Event management within QA-CAPA Center Of Excellence, responsible for processing/suppor...
We re looking for people who are determined to make life better for people around the world.Business/Customer Support: Understand and anticipate the scientific information needs of all local/regional customers (payers, patients, health careproviders) and actively address their questions in a timely fashion by leading data analyses and new clinical or healthoutcomes research efforts. Contribute to...
About Thermo Fisher Scientific:At Thermo Fisher Scientific, each one of our 130,000 extraordinary minds have a unique story to tell. Join us and contribute to our singular mission enabling our customers to make the world healthier, cleaner and safer.When you re part of Thermo Fisher Scientific, you ll do challenging work, and be part of a team that values performance, quality and innovation. As p...
Ready to shape the future of clinical trials? Dive into a dynamic role where your negotiation finesse and budget expertise will take center stage. Join us at Novo Nordisk and be a catalyst for ground-breaking advancements in healthcare. Apply now your career evolution starts here! The Position Your main activities will include negotiation contract language and budget directly with clinical sites,...
Ready to shape the future of clinical trials? Dive into a dynamic role where your negotiation finesse and budget expertise will take center stage. Join us at Novo Nordisk and be a catalyst for ground-breaking advancements in healthcare. Apply now your career evolution starts here! The Position Your main activities will include negotiation contract language and budget directly with clinical sites,...
Ready to shape the future of clinical trials? Dive into a dynamic role where your negotiation finesse and budget expertise will take center stage. Join us at Novo Nordisk and be a catalyst for ground-breaking advancements in healthcare. Apply now your career evolution starts here! The Position Your main activities will include negotiation contract language and budget directly with clinical sites,...
Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions Manage staff in accordance with organization s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professi...
Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives.Essential Functions Manage staff in accordance with organization s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professi...
About Thermo Fisher Scientific:At Thermo Fisher Scientific, each one of our 130,000 extraordinary minds have a unique story to tell. Join us and contribute to our singular mission enabling our customers to make the world healthier, cleaner and safer.When you re part of Thermo Fisher Scientific, you ll do challenging work, and be part of a team that values performance, quality and innovation. As p...
Main purpose of the job:To upgrade and maintain all Quality Assurance and Quality Control processes for the Wits VIDA LaboratoryLocation:Wits Vaccines & Infectious Diseases Analytics (VIDA) Research Unit, Chris Hani Baragwanath Academic Hospital, Soweto - JohannesburgKey performance areas:Laboratory Quality Assurance and Quality ControlEnsure that the Wits VIDA Laboratory complies with all applic...
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory r...
Additional information:The MRC/Wits Rural Public Health and Health Transitions Research Unit (Agincourt) is an exceptional health and population research centre in the Wits School of Public Health. The Unit supports a major research infrastructure underpinned by a health and socio-demographic surveillance system (HDSS), a form of longitudinal population registration, covering a substantial portio...
Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...
Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...
Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...
Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 cou...
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General Description: The Country Medical Director will be accountable for medical affairs a...
JOB OVERVIEWThe Associate Manager, Site Solutions supervises and manages an assigned team of Clinical Trial Payments staff who manage or support studies to ensure quality, time and budget deliverables are met. Work with staff to ensure that all assigned project deliverables are completed ensuring quality deliverables on time and in accordance with Standard Operating Procedures (SOP), policies and...
When our values align, there's no limit to what we can achieve. Parexel FSP is currently hiring for a Study Operations Manager II, home-based.Permanent, full-time.Single sponsor dedicated to a worldwide biopharmaceutical company that relentlessly seeks breakthroughs to improve patients lives. Their daily innovation contributes to a healthier global community. This is the space where today s visio...
When our values align, there's no limit to what we can achieve. Parexel FSP is currently hiring for a Study Operations Manager I, home-based.Permanent, full-time.The Study Operations Manager I (SOM I) has responsibilities for study-specific country-level activities from study startup through conduct and study close on studies of limited complexity.Single sponsor dedicated to a worldwide biopharma...
A Medical Insurance Company in Benoni, Gauteng is looking for a Medical Officer who will provide confidential clinical advice to patients, review medical reports, and provide treatment plans. Key Tasks Initiate and analyse treatment plans. Review medical reports and provide treatment plans. Explain and discuss test results or prescribed treatments with patients. Monitor patient progress and respo...
Marketing Manager (for Patient Recruitment) Wanted: Shape the Future of Medical Research 100% remote, forever Unlimited paid leave Total compensation 20% above market Hello we're Trialfacts , a remote, entrepreneurial company playing a crucial role in advancing medical research. We're on the lookout for a Marketing Manager (for Patient Recruitment) with extensive experience in B2C health marketin...
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