Oeiras, Portugal \| Full time \| Hybrid \| R1533156

IQVIA is the world leader in the provision of health and pharmaceutical data to the health care sector. Our Real-World Solutions department is globally renowned for providing business focused research, conducted to the highest standards. IQVIA delivers a suite of services to help healthcare stakeholders access and apply real-world evidence for decisions at every stage of the product life cycle. The Real-World Solutions team is focused on providing innovative solutions for Market Access, medical, and scientific teams.
The RWS Portugal team is a diverse, multi-disciplinary team dedicated to excellence through teamwork by supporting the delivery of a wide range of client projects in the pharmaceutical industry in Portugal, including medical department and/or market access projects, retrospective database studies, business strategy, patients’ registries, and other varied and exciting engagements.Working with other team members you will:* Contribute to study design and methodology development.

• Develop innovative approaches, frameworks, and solutions to client problems.
• Assist in the preparation of study protocols and draft reports.
• Analyze and interpret qualitative and quantitative ‘real-world’ data for deliverables.
• Conduct ad-hoc project tasks.
• Prepare presentations, abstracts and manuscripts relating to projects including for presentation at scientific conferences and submission to scientific journals.
• Conduct primary and secondary research.
• Conduct workshops and moderate discussions.
• Present results to external clients.
• Assist with overall project management and client management.
• Attend client and other external meetings normally accompanied by a colleague.
• Review and analyze client requirements or problems in order to help develop proposals for projects.
• Produce initial drafts of proposals based on client RFPs and supporting information.
• This position requires some degree of travel within Portugal (20% FTE).

Our desired profile:

Experience:* +2 years of experience undertaking clinical research activities at site or in the pharmaceutical industry in a relevant area such as RWE/RWD, Clinical Operations or Epidemiology.

• Experience in at least one of the following environments: Healthcare Consultancy, Pharmaceutical or other Healthcare Industry, Academic or Governmental Research Organization, Health Services Research setting.