IQVIA Hiring Biomedical Clinical Research Associate in Saudi Arabia Salary starts from SAR 152,519/year Apply Online

Company:	IQVIA
Job Role:	Clinical Research Associate.
Experience:	(1-2 years).
Vacancy:	20+
Qualification:	Bachelor's degree in a health care or other scientific discipline or educational equivalent.
Salary:	SAR 152,519/year.
Location:	Riyadh - Saudi Arabia.
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Apply Mode:	(Online)
Deadline:	Not Mentioned

About the Company:

IQVIA uses data, technology, advanced analytics, and expertise to help customers drive healthcare forward. Together with the companies we serve, we are enabling modern, more efficient, and more effective healthcare, and creating breakthrough solutions that transform business and patient outcomes. Diverse skills and an open mind are required to get there. Everyone at IQVIA, including our colleagues at Q2 Solutions, contributes to our shared goal of improving human health. It is a pleasure to work with you.

Job Description:

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Responsibilities:

Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with the contracted scope of work and good clinical practice.

• On a site-by-site basis, may be responsible for developing the project subject recruitment plan. Adapt, drive and track the subject recruitment plan in line with project needs to enhance predictability.
• Monitoring visits and site management for a variety of protocols, sites, and therapeutic areas.
• Set up regular lines of communication with assigned sites to manage ongoing project expectations and issues. Train sites on protocol and related study topics.
• Assess the quality and integrity of study site practices related to the proper conduct of the protocol and compliance with applicable regulations. As appropriate, escalate quality issues.
• Monitor the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Supports the start-up phase.
• Manage and maintain appropriate documentation regarding site management, monitoring visit findings and action plans, by submitting regular visit reports, generating follow-up letters, and other required study documentation.
• Build awareness of the site's features and opportunities for study.
• As appropriate, collaborate and liaise with members of the study team regarding project execution.

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

Did You Know?

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Required Knowledge, Skills And Abilities:

• Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; e.g.,
• Guidelines of the Good Clinical Practice (GCP) and the International Conference on Harmonization (ICH)
• Training provided by the company provides good therapeutic and protocol knowledge
• Competence in Microsoft Word, Excel, and PowerPoint, as well as the use of a laptop computer
• Communication skills, including written and verbal
• Organizational and problem-solving skills
• Time management skills that work
• Establish and maintain effective working relationships with colleagues, managers, and clients

Minimum Required Education And Experience:

• Bachelor's degree in a health care or other scientific discipline or educational equivalent,
• At least 2 years of CRA experience of on-site monitoring visits,
• Travels frequently to sites
• Excellent command of the English language
• Prefer location: Riyadh.

#CRASDAJD

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com. 

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