IQVIA

Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers. Prepares and maintains core clinical trial submission More...

Responsibilty: Meeting with the software development team to define the scope and scale of software projects. Designing software system architecture. Completing data structures and design patterns. Designing and implementing scalable web services, applications, and APIs. Develo More...

Excellent salary and benefits package Company car or car allowance Depending on the model, home-based is a possibility Flexible working hours in a home-based role As a CRA, you will receive a company iPad and have use of key developments such as site visit apps, visit reporting More...

Strong written and verbal English and Arabic skills. Substantial industry/academic experience building machine learning algorithms Previous experience in managing complex projects and leading a team of 2-4 data scientists. Prior experience and keen interest in working directly wi More...

Working closely with the clients in Saudi Arabia, building up working relationships with the key stakeholders in the region, and leading the data science workstreams on this project. This will involve leading a remote sub-team of 3-4 data scientists who will be based across the US, More...

Complete appropriate therapeutic, protocol and clinical research training to perform job duties. Gain experience in study procedures by working with experienced clinical staff. Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out More...

This is a prominent client facing role in the Global MedTech Device Consulting Center of Excellence You work with clients, IQVIA consulting peers and IQVIA account management to provide value added input as a trusted advisor You generate and close commercial consulting opportuniti More...