Ich Q7 Jobs in Amman

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 More...

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 More...

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 More...

Typical Accountability Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies Leads and optimises the performance of the Local More...

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 More...

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 More...

Accountabilities: You will facilitate key discussions with various stakeholders, provide SME technical support on system testing of the Core EDC Product, and manage data integrations. You will perform impact analysis for any changes to the EDC system and work with the business to More...

Accountabilities: As a Quality Engineer Specialist, you will facilitate and guide cross-functional team members in the use of available quality risk management tools, including FMEA, PHA, RR&F. You will collaborate with project teams and necessary departments to complete ri More...

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 More...

About the job Responsibilities Lead and coordinate a cross-functional study team of experts in accordance with STOM and its roles, accountabilities and responsibilities framework (RACI) to ensure the clinical study progress as planned driving achievement of milestones acco More...

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 More...