CRA (R1104951)

Job Description

IQVIATM 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.

Clinical Research Associate

Job description: Clinical Research Associate (CRA)

Contract: full-time based

Salary: based on experience

Location: Casablanca, Morocco

Company:

IQVIATM is The Human Data Science CompanyTM, 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.

You will work in the Real-World Insights (RWI) business unit. The team is over 80+ consultants with various capabilities in real-world evidence, epidemiology, market access and health economics.

Role summary:

As part of a project team, you will perform observational studies with primary data collection according to our standard operating procedures (SOP). You will work closely with the project manager:

• Monitor site activities with the project manager (training, patient inclusion, queries, data monitoring, study closing...)

• Initiate investigator site activities, including collection and submission of regulatory documents, customization of informed consent documents, obtain fully-executed contract, track and ensure site compliance to required training, and effectively drive timelines aligned with our priorities

• Communicate directly with sites to enable start-up and maintain an active collaboration during the study

• Ensure country-specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

• Support the project manager in the study coordination (newsletter, client reporting...)

• Populate and review electronic case report forms (eCRF)

• Understand and comply with procurements, legal and financial requirements and procedures

Education:

Bachelor’s degree in a scientific or health-related field, with a validated training as CRA.

Experience:

Prior experience of working in investigator site management, from either a pharmaceutical company or a CRO environment.

Skills:

Strong communicative skills, orally and in writing, both in French and in English

Good level of practice with Office tools: Excel, Access, Word, PowerPoint

Detailed and solution-driven, quality and service-oriented way of working with scientific rigor

Ability to manage timelines and quality of work using organizational skills, while working on several projects in parallel

Team player, able to integrate in an international and multidisciplinary team

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.