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,
Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside
Novo Nordisk South Africa is seeking an experienced SSU Manager to shape and lead the SSU Unit within the Clinical Development Centre (CDC) in Johannesburg. You will direct study start-up operations, regulatory submissions, and drive continuous
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management for global clinical trials. This remote/WFH role provides company equipment and a competitive, incentive-based compensation package. You will lead cross-functional teams, ensure data quality and
IQVIA is looking for Clinical Data Management Leads to oversee data management for global clinical trials. This is a fully remote role where you will manage timelines, budgets, and client interactions, ensuring compliance and quality in delivering data-driven
IQVIA is hiring multiple Clinical Data Management Leads for remote delivery models. You will oversee end-to-end data management for global trials, ensuring quality and compliance while leading cross-functional teams. Expect client interaction as the main data management contact
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams
IQVIA LLC is hiring multiple Clinical Data Management Leads for remote roles across our delivery models. You will lead data management for complex, global clinical trials from study setup to database lock. As the main client contact for
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You’ll ensure quality, accuracy, and regulatory compliance while leading cross-functional teams that help bring new therapies to life. This is
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,
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
The Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. External data streams include but
Job Description Job Title EXPORTS: TECHNICAL AND DEVELOPMENT LEAD Reporting To EAF EXPORT MANAGER Function EXPORTS: TECHNICAL SUPPORT AND R&D Location GAUTENG ABOUT UPL: UPL is focused on emerging as a premier global provider of total crop
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on
National Veterinary Services Manager The success of a company depends on the passionate people we partner with. Together, lets share our talents. As a global leader in animal health, Ceva Animal Health believes our success is linked
Interested in a career that matters? Interested in a career that matters? At Novonesis, we believe biological solutions can help transform the way the world produces and enjoys beverages. As an Industry Technical Manager, Beverages, you
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 clinical
Interpath is an international and fast-growing advisory business with deepexpertisein a broad range of specialisms spanning deals, advisory and restructuring. We deliver tangible results for global businesses, their investors and stakeholders when complex problems arise and critical
Job Description As a Senior Scientist you will coordinate and manage the customer product development projects, supporting the development process from the generation of concepts, to creation of laboratory samples, through to industrial manufacturing. Supporting and
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