وظائف في تنظيمي في عمّان

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...

Key Accountabilities: Key Accountabilities: (Describe the important end result of the job, WHAT & WHY. Suggested 8 – 16 ideal responsibility) - Monitor and manage the internal regulatory environment in making all necessary analysis in order to assess the impact of the r المزيد...

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and 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...

Our Chemistry, Manufacturing, and Controls (CMC) Regulatory function spans across the product lifecycle and are responsible for the regulatory strategy relating to the development, manufacture and testing of all of our medicines. With our expertise we interpret, anticipate and sh المزيد...

Responsibilities: Collect & Coordinate information to prepare submissions of CTD & e-CTD as per recent HA requirements (JFDA experience is an advantage) Review drug substance master file for compliance with specific HA & ICH guidelines. Contact and follow up with othe المزيد...

ضمان اتخاذ القرار الأمثل لمركز الخليج للأبحاث من خلال دعم التسليم والملكية المناسبين (الصيانة والتحكم) لمركز بيانات الامتثال (بحيرة البيانات). إجراء التنقيب عن البيانات باستخدام أحدث الأساليب وتعزيز إجراءات جمع البيانات لتشمل المعلومات ذات الصلة ببناء الأنظمة التحليلية. التحقق من ج المزيد...

What You’ll Do This role is an opportunity for an experienced pharmaceutical regulatory affairs professional keen to move into a global organisation with a strong pipeline in Oncology, Cardiovascular, Immune Therapies and Respiratory. As a Senior Regulatory Affairs Assoc 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...

Accountabilities: As a CMC RA Manager, you will manage the timely preparation and delivery of CMC contributions to regulatory submissions linked to medicinal products throughout their lifecycle. You will be accountable for delivering “submission ready” CMC modules t المزيد...

Accountabilities: As a Senior IT Quality Manager, you will use your pharmaceutical regulatory compliance experience and intelligence to support and deliver an integrated IT QM strategy. You will be responsible for understanding and applying regulatory compliance policies and st المزيد...

About the job Company Description We suggest you enter details here. Role Description This is a full-time on-site role as a Governance Manager located in Riyadh. The Governance Manager will be responsible for overseeing and implementing governance policies and procedur المزيد...

تنفيذ الرؤية الإستراتيجية لمنتجات وخدمات WM الاستثمارية بما يتماشى مع الأهداف والغايات العامة للبنك، من خلال تطوير العروض والحلول المصممة خصيصًا لمختلف قطاعات وأسواق البنك التجاري. إجراء أبحاث السوق وتحليل المنافسين وتعليقات العملاء لتحديد الفرص المتاحة للمنتجات الجديدة أو التحسينات 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...

Responsibilities Manage and lead the insurance contract review process for the company Ensure compliance with company standards and regulatory requirements Identify and address any deficiencies in deductibles, limits of liability, and sums insured Make recommendations to corre 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...

تخطيط التدقيق وتنفيذه: - تطوير خطط واستراتيجيات التدقيق بناءً على الأهداف التنظيمية والمخاطر والمتطلبات التنظيمية. إجراء عمليات تدقيق شاملة لأنظمة وعمليات وضوابط تكنولوجيا المعلومات لتقييم الامتثال والفعالية. تنفيذ إجراءات التدقيق، بما في ذلك المقابلات ومراجعة الوثائق والاختبار والتح المزيد...

تحديد المخاطر البيئية والاجتماعية والحوكمة وتقييمها: تطوير وتنفيذ أطر لتحديد وتقييم ومراقبة المخاطر البيئية والاجتماعية والحوكمة. إجراء تقييمات شاملة للمخاطر البيئية والاجتماعية والحوكمة للعملاء والمشاريع والمنتجات الجديدة والحالية. التعاون مع الإدارات المختلفة لضمان أخذ المخاطر الب المزيد...

Typical Accountabilities Owning the delivery and oversight on a study /indication, potentially as a Global Project Statistician for a standard drug project Contributing to statistical methodological advances Lead the statistical thinking and contributions to the delivery of المزيد...

Key Responsibilities: Lead the hiring process and assemble a high-performing development team for our new Jordan Office, ensuring the recruitment of top talent to drive our technological and business goals. Lead and manage a team of developers, architects, and engineers in the المزيد...