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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...

خبرة في إدارة مشاريع الصحة والتكنولوجيا. خلفية في مجال الرعاية الصحية، مع التركيز على تكامل النظام. إتقان اللغة العربية. القدرة على العمل في بيئة متعددة الثقافات ومتعددة الجنسيات. مفتوح للانتقال إلى الأردن أو المقيمين حاليا في الأردن. الالتزام بمشروع لمدة عام واحد في الأردن، مع إمكان 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...

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...

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...

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...

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...

What you’ll do: Manage contracting with third-party lab service providers for assay development and validation, and work with business operations, procurement, and clinical operations to ensure appropriate SOWs and contracts are put in place for sample analysis of clinic المزيد...

What you’ll do: Lead, provide guidance, and delegate appropriately to a cross-functional study team or supervise outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and qualit المزيد...

You will also contribute to advisory boards to ensure there is engagement with site-specific KEEs to ensure robust study designs, recruitment strategies. Essential Skills/Experience: Bachelor’s degree with focus on life sciences or equivalent Industry or academic exp المزيد...

Accountabilities: In this role, you will apply scientific knowledge and insights relevant to therapeutic areas, healthcare systems, products, disease state management, emerging therapies, and the competitive landscape. You will collaborate with key internal Global Medical Affairs المزيد...