Regulatory Reporting Jobs in Riyadh

. Responsible for the coordination of submissions to Regulatory Authorities and Ethics Committees in the assigned regions and ensures quality of regulatory documentation . Provides regulatory support regarding start up activities and maintenance in the assigned clinical projects and More...

Education: Bachelor's degree in business administration or related field, specialized certifications in project management or organization may be beneficial. Previous experience: Experience working in the field of organization or management for a specific period of time, preferab More...

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea More...

Overseeing Accounting Operations: Manage all aspects, including Billing, A/R, A/P, GL, Cost Accounting, Inventory Accounting, and Revenue Recognition. Leading Budget and Financial Forecasts: Direct the preparation of our budget and financial forecasts, reporting on variances. Publ More...

Compiling and submitting in a timely manner, all regulatory documents on behalf of Baxter Company Limited in line with regulatory requirements. Respond to any regulatory queries within strictly provided deadlines. Maintain regulatory files in a format consistent with company and SFD More...

Collaborate with our regional and local IT colleagues to identify business priorities and determine how information sciences and analytics can be applied to support these priorities Make strategic decisions on the use of Data and Information Sciences techniques in solving critical More...

Education and qualifications: University degree in a related field such as management, finance, computer science, or statistics. Strong quantitative analysis and modeling skills, with good knowledge of data management and reporting software. Knowledge of tools and techniques: Profic More...

This individual will be a dynamic, go-getter with Corporate Communications experience who can self-manage, loves to collaborate and ideate, and thrives off of carrying a lot of responsibilityManage and collaborate with public relations agency; set PR strategy and manage to outcomes.Ma More...

As a Principal Regulatory Writer, you will play a pivotal role in translating complex scientific and clinical data into compelling regulatory documents. Your expertise will be crucial in ensuring compliance with European regulations and industry standards. Key Responsibilities: More...

Due to increasing demand for metal roofing systems in Atlantic Canada, Maritime Permanent Roofing is looking to immediately expand our installation team. Be your own boss!Join one of the top installers of metal roofing systems in North America. Maritime Permanent Roofing is looking fo More...

Identify the misalignments and potential issues present in the reports, to generate a view of the areas of attention to escalate to the Planning & Integration Director Support the Business Partners in the management of the governance forums by ensuring that all governance meeti More...

In alignment with the Hiring Manager, is responsible for developing and implementing regulatory strategic plans for product registration and lifecycle management. Lead the preparation of regulatory submissions including New Drug Submissions (NDSs). Provide regulatory inputs and g More...

Recommends changes for labelling , manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking/control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Re More...

Bachelor’s degree in Life Sciences, Engineering, Technical Writing, or a related field; advanced degree preferred Minimum of 6 years of experience in regulatory writing, preferably within the medical device industry Strong understanding of regulatory requirements and guideli More...

Preparation of project plan and Timelines for Quarterly and Annual reporting inline with expectation from Board Audit Committee (BAC) and Board of Directors (BoD). Ensure preparation and timely review and closure of Quarterly and Annual Financial statements. High level review of i More...

University degree in a related field such as business administration, data science, economics, or any related discipline. Strong analytical skills and ability to interpret data and extract key aspects and trends from it. Knowledge of reporting tools and software used to analyze data, More...

Identifies information sources and resources for local regulations. Collects and coordinates information on regulatory requirements for in vitro diagnostic devices, quality, preclinical and clinical data to meet applicable regulations. Assist in device registration activities - ag More...

About Zahrawi GroupZahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE KSA Qatar Bahrain & Oman markets. The company supplies and distributes highquality products and services to Hospitals Clinics Laboratories & Analytical Industries. job More...

Responsible for products registration, renewals, and ensuring approvals via GHAD systems and other SFDA systems, including reimbursement follow up if any. Responsible for the post-market surveillance of medical devices for all related reports in accordance with the regulatory agenc More...

University degree in Business Administration, Economics, Data Science, Industrial Engineering, or any related discipline. Strong knowledge of transformation planning and reporting methods and tools, such as project management techniques and data analysis models. Ability to analyze dat More...