Biostatistical Data Specialist
- Location: Greece, Bulgaria, Estonia, Portugal, Spain.
- Work Model: Hybrid or Office based
The role:
Manage, develop, recommend, and implement standard procedures, measures of performance, clinical data harmonization, QC, and analysi. Organize and allocate resources according to multi-project requirements and deadlines. Serve as lead statistical consltant on projects.
Essential Functions
• Technical responsibilities:
i) Serve as a Statistical consultant for other members of the department and staff members from other Biostatistics departments within the company.
ii) Maintain knowledge and awareness of developments in statistical programming.
iii) May participate as high level lead Stat on major project(s).
iv) Provide advanced technical expertise for internal and external clients.
vi) Provide expert review of process and methodology development work with regard to Statictical standards and validation procedures.
• Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resource matters.
• Participate in project meetings; keep up-to-date on project issues; keep Director informed of project issues.
• Coordinate and participate in process improvements and interoffice/interdepartmental task forces; oversee collection and reporting of Stat metrics, implementation of revised work practices, new guidelines, and new software tools as they become available.
• Effectively recommend resource allocation at the site level so as to achieve target utilization rates and project realization rates.
• Assist in the following: (i) sales meetings as required; (ii) overseeing proposal preparation; (iii) ensuring that all proposals bid by the department have an adequate budget, and sufficiently detailed set of budget assumptions.
Qualifications
• Master's Degree Computer science or related field and 5 years relevant experience including 1 year in a leadership capacity
• Bachelor's Degree Computer science or related field and 6 years relevant experience including 1 year in a leadership
• Equivalent combination of education, training and experience in lieu of degree
• Advanced knowledge of R and technical database skills
• Knowledge of statistics and/or the clinical drug development process
• Excellent written and oral communication skills with good interpersonal skills
• Very good problem solving skills
• Excellent presentation skills
• Sound judgment/decision making
• Ability to lead and motivate a team
• Ability to effectively delegate work
• Ability to effectively motivate other staff members
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
JOIN US!
In return, we’ll provide the support for you to develop your programmer career in a supportive and dynamic environment. You’ll be working in a global company of over 75,000 employees in more than 100 countries, with a broad range of healthcare information, technology and service offerings.
You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately, improve outcomes for patients.
Whatever your career goals, we are here to ensure you get there!
#LI-Hybrid or #LI-Onsite
#LI-MH5
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
