Clinical Trial Assistant / Senior Clinical Trial Assistant (R1124416) in Beirut, Lebanon at IQVIA™

Date Posted: 3/25/2020

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Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

We are currently looking for an experienced Clinical Trial Assistants / Senior Clinical Trial Assistants who will join our team in Lebanon. This is role is a great opportunity for the experienced Clinical Trials Assistants to work in a leading pharmaceutical company. We are looking for a person who has experience with TMF management and study package submissions to authorities.


  • Set up and maintain applicable TMF

  • Maintain, update, and input information and/or documents into applicable databases for clinical trial and/or data tracking; ensure reporting system records and quality standards are appropriately maintained.

  • Prepare and compile dossier for initial HA and IRB submission or amendment and oversee associated activities, responses and communications with obtaining approvals for the assigned country(ies).

  • Track incoming and outgoing clinical and regulatory documents/updates for investigator sites, studies, or project team .

  • Provide support for trial budget and investigator site payments; support the project manager and team with financial tasks.

  • May ensure the successful negotiation and ongoing management of clinical disclosure agreements with investigative sites .

  • Operates largely in transactional activities with oversight.


  • University degree in life sciences preferably or country’s educational equivalent and CTA experience; or equivalent combination of education, training and experience
  • At least 2 years of experience in Global Clinical Trials
  • Good understanding of clinical trial processes
  • Fluent English (written and spoken)
  • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
  • Effective time management and organizational skills
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1124416