Current Jobs at IQVIA

• The Project Coordinator will be expected to perform a variety of tasks with multiple reporting requiring health diplomatic skills, understand multiple country travel, visa and work permit requirements for consultants’ deployment. 

Project Coordinator Responsibilities: 

• Coordinate internal processes, resources, WHO and multiple country requests and needs for the flawless execution of recruitment and rapid deployment of multiple consultants.  
• Ensure that all recruitments and deployments are undertaken and delivered on-time, within scope and with adequate logistical, per diem and other monetary support. 
• Assist in the review of progress against the scope and objectives, involving all relevant internal departments and WHO/AFRO and ensuring feasibility of agree next steps. 
• Ensure resource availability and allocation for the relevant country consultant recruited and deployed with rapid response. 
• Develop a detailed plan to monitor and track progress on recruitment and deployment of consultants.  
• Manage changes to the project scope, project schedule, and project costs using appropriate verification techniques. 
• Support and provide adequate guidance and information to the Project Assistant on travel plans, and arrangements, expenses and reimbursements, insurance, visa etc.
• Profile by Country and perform risk management to minimize potential risks for consultants and escalate as necessary. 
• Perform other related duties as assigned by the Project Lead and WHO/AFRO Point of Contact Develop spreadsheets, diagrams and process maps to document needs. 

Project Coordinator Requirements: 

• 3- 5 years of proven working experience in project coordination 
• Team management and monitoring  
• Performance management and processing performance-based remuneration 
• Excellent client-facing and internal communication skills 
• Excellent written and verbal communication skills 
• Sound organizational skills and ability to multi-task. 
• Computer competency in use of all Microsoft Office 
• Bachelor's Degree in relevant field of study,
• Experience with project management software tools. 

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Responsibilities:

• Import data from various sources
• Program quality control checks for source data and reporting data issues
• Interpret project level requirements and develop programming specifications
• Write programming code following established Good Programming Practices
• Program SDTM and ADaM datasets
• Program to create statistical analysis tables, listing and figures
• Validate datasets and all statistical outputs per prescribed gate checks
• Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines
• Use and promote the use of established standards, SOPs, and standard methodologies
• Export data and clinical study report materials
• Provide training and mentoring to team members and department staff
• You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.

THE PERSON

• We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming.

Key required skills include:

• Home Based/Remote
• 5+ experience in Statistical Programmer role from CRO/Pharma with ADaM/SDTM/ TLFs
• Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication.
• In light of the above, candidates for the roles should exhibit the following skills and competencies:
• Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
• Knowledge of statistics and exhibit routine and occasionally complex analytical skills
• A focus on quality, accuracy, and completeness of work activities 
• Excellent communication skills
• A good understanding of Good Clinical Practice and ICH guidelines