وظائف في Clinical Setting في عمّان

The CSA Team Lead is responsible for line managing dedicated group(s) of staff and responsible for planning and utilization of staff resources, assigned budget, objective setting and performance follow-up. It is also expected that the CSA Team Lead may contribute to regional/gl المزيد...

Main Responsibilities, will include but will not be limited to: essing, observing, and speaking to patients Recording details and symptoms of the patient medical history and current health Preparing patients for exams and treatment Creating, implementing, and evaluating patient المزيد...

Typical Accountabilities The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and commun المزيد...

Typical Accountabilities Responsible for implementing aligned vendor management and alliance strategy. Identify potential space for improvement and implementation excellence, accelerate strategy implementation and maximize value creation to clinical trial delivery. Manage routin المزيد...

Agree and deliver plans for projects / programmes (or contribution in part to a larger project), including activities, resources, costs, roles, responsibilities and quality as defined in the IT Project Management Methodology (ADF). Lead project / programme budgets, forecasts, tas المزيد...

Responsibilities Provide strategic leadership and operational oversight to the Global Clinical Operations team. Develop and implement standard operating procedures (SOPs) in line with regulatory compliance requirements, Good Laboratory Practice (GLP), Good Clinical Practice (GC المزيد...

A CRA with longer tenure and experience may take on additional responsibilities that include additional tasks associated with Local Study Manager. Typical accountabilities: Contributes to the selection of potential investigators. In some countries, as required, CRAs are ac المزيد...

Accountabilities: As a Clinical Programmer II, you will design, develop, implement, and validate programs created in SAS/Python/R/SQL or dashboard applications such as PowerBI/Spotfire/MicroStrategy. You will process, analyze and report clinical trial data for review by clinical المزيد...

About the job Conduct monitoring visits (remote and in the field), as well as start-up and closing visits to study centers in compliance with the Monitoring Plan, company procedures, Good Clinical Practices and local regulations. Trains, supports and advises researchers and ce المزيد...

Responsibilities will include: Influencing the design phase with relevant experts to drive an optimized supply chain design with respect to quality, risk and cost for the business Working in conjunction with the Supply Chain planner to guarantee: Balancing Short to Mid-term المزيد...

Work you will do You will work with our practice leaders and professional consultants as a team to solve complex business problems and deliver high quality solutions to our clients on areas including but not limited to: Digital Transformation and Intelligent Automation Insu المزيد...

About the job POSITION TITLE: Regulatory Operations Specialist II DEPARTMENT: Ora Europe LOCATION: UK or Europe Ora Values the Daily Practice of... Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor The Role: The Regulatory Opera المزيد...

We welcome new ideas and innovations to help us continue to add value. Our ultimate goal is to deliver products and novel insights to improve patient’s lives. Key Responsibilities Lead cross-disciplinary project teams in a complex matrix organization to deliver proje المزيد...

تعزيز علاقتنا مع العملاء وشراكات الشركة تخطيط وتنفيذ الحملات والفعاليات تتبع وتحليل والإبلاغ عن نجاح تلك الحملات والأحداث إنشاء محتوى تسويقي عبر الإنترنت وغير متصل قم بتمكين فريق المبيعات بالمحتوى التسويقي والحملات التي تساعد في زيادة المبيعات المزيد...

You’ll be working with many different modalities beyond classical biopharmaceuticals, so you’ll need to be creative and work in areas where there are no pre-defined solutions, utilising the best capabilities within and outside AstraZeneca. Your main tasks will inclu المزيد...

Typical Accountability Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies Leads and optimises the performance of the Local المزيد...

The role holder is accountable for ensuring that all activities are delivered demonstrating behaviours and values aligned to AstraZeneca Code of Conduct and supporting policies, standards and procedures, including compliant management of Budget, Safety, Health and Environment. Ty المزيد...

The role holder is accountable for ensuring that all activities are delivered demonstrating behaviours and values aligned to AstraZeneca Code of Conduct and supporting policies, standards and procedures, including compliant management of Budget, Safety, Health and Environment. Ty المزيد...

About the job Responsible for products’ clinical development strategy and plan in multiple disease areas in R&D China. Responsible for managing reginal or China therapeutic or research projects or acting as an expert involved in the design, conduct, monitoring, data in المزيد...

Accountabilities: As a Senior Standards Developer I, you will develop and maintain one or more median/high complexity analysis and reporting standards. You will monitor and update requests within a defined system, perform independent quality control, and lead the quality of your المزيد...