Clinical Research Jobs in Jordan

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...

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 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...

1. Bachelors in medicine / Internal medicine is a plus with at least 2 years’ experience after obtaining practicing license in medicine. 2. Good knowledge of GCP guidelines. 3. Good knowledge of the text and corresponding implementation of the most recent version of the World More...

Work you will do You will work with our practice leaders and professional consultants as a team to solve complex business problems and deliver high quality solutions to our clients on areas including but not limited to: Digital Transformation and Intelligent Automation Insu More...

You will also contribute to advisory boards to ensure there is engagement with site-specific KEEs to ensure robust study designs, recruitment strategies. Essential Skills/Experience: Bachelor’s degree with focus on life sciences or equivalent Industry or academic exp More...

Experience in managing Health & Technology projects. Background in healthcare, with a focus on system integration. Proficiency in Arabic. Ability to work in a multicultural, multinational environment. Open to relocating to Jordan or currently residing in Jordan. Commitment More...

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 More...

Key Responsibilities and Requirements: . Maintain quality standards to preserve the integrity of data and findings. . Writing articles research in English and Arabic. . Analyze data using various statistical methods. . The candidate must be able to write articles in all fields. More...

The role holder is accountable for ensuring that all activities are delivered demonstrating behaviours and values aligned to AstraZeneca Code of Conduct and supporting policies, standards and procedures, including compliant management of Budget, Safety, Health and Environment. Ty More...

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 More...

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 More...

Proven Experience: Demonstrated experience in digital marketing, social media management, email marketing, or related fields is essential. Candidates should have a track record of successfully managing digital engagement campaigns and driving measurable results. Digital Marketing S More...

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 More...

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...

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...

Company Description Tarabezah is a mobile application that helps users find and reserve hangout places in Amman, Jordan. With a wide selection of restaurants, lounges, and cafes, Tarabezah offers a user-friendly and up-to-date platform that satisfies customer demands. Users can earn More...

As a Senior Research Scientist you will propose experimental strategies and have the possibility to be creative in solving a wide range of synthetic challenges. You will plan, prioritize and perform your own work and actively collaborate with the project team by driving problem sol 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...

Bioanalytical Team leader Pharmaceutical Research Unit (PRU) or Arab Pharmaceutical Industry Consulting (APIC) is a leading clinical research organization (CRO) that was established in Jordan in 1993. At PRU/APIC we offer clinical development solutions that aim to transform drug d More...