وظائف في Clinical Documentation في عمّان

Role Description This is a full-time on-site role for a Senior Documentation Specialist located in Amman, Jordan. The Senior Documentation Specialist will be responsible for day-to-day tasks associated with clinical documentation, online visa applications, immigration petitions, docu المزيد...

مهارات التوثيق عبر الإنترنت والتوثيق الفني مهارات تحليلية قوية مهارات الكتابة الفنية مهارات اتصال ممتازة الكتابية والشفوية موجهة نحو التفاصيل ومنظمة الخبرة في مجال الهجرة تعتبر ميزة إضافية. آيلتس 6.5 المزيد...

Job Experience And Competency Requirements Excellent written & verbal English is a must Experience in forwarding for 1 – 2 years A university degree in a related field or Business Administration Presentable and dynamic Excellent computer skills

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...

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...

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...

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...

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...

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...

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...

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...

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...

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...

Accountabilities: As a Senior Statistical Programmer I, you will collaborate with other team members to provide programming support to deliver technical programming and information components of a study or a project deliverable. You will implement statistical programming aspect المزيد...

All System Owners will lead and manage improvement projects as needed, and will contribute to functional, regional and or global initiatives. Typical Accountabilities System Ownership: As the allocated owner for a specific clinical computerized system: Accountable for th المزيد...

As a CMC Regulatory Affairs Manager, you will manage the production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges. You will manage global CMC regulatory submissions ensuring that project activities and documentation are delivered to the المزيد...