وظائف في Clinical Documentation Improvement 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...

تصميم وتوثيق وصيانة وثيقة/دليل الممارسة والسياسات. تحديد وتنفيذ ومراقبة مؤشرات الأداء الرئيسية لكفاءة الممارسة. إنشاء وقيادة برنامج التوعية بالتدريب العملي في جميع أنحاء المنظمة. ضمان الالتزام والامتثال للمتطلبات القياسية وسياسات العملية. العمل كخبير في هذا الموضوع لهذه الممارسة المزيد...

Job Summary: The role involves analyzing and collaborating closely with Team Leaders and the Pod Manager to identify improvement opportunities. This includes offering actionable insights to enhance customer experiences and addressing gaps in processes or knowledge. Responsib 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

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...

الخبرة المثبتة: تعد الخبرة المثبتة في التسويق الرقمي أو إدارة وسائل التواصل الاجتماعي أو التسويق عبر البريد الإلكتروني أو المجالات ذات الصلة أمرًا ضروريًا. يجب أن يتمتع المرشحون بسجل حافل في إدارة حملات المشاركة الرقمية بنجاح وتحقيق نتائج قابلة للقياس. مهارات التسويق الرقمي: الكفاء 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...

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...