Bachelor’s degree in life sciences/healthcare (or clinically relevant degree) is strongly preferred. Advanced degree is preferred.
Languages:
Fluent English, oral and written
Experience/Professional requirements:
≥ 2 years of recent involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV of standard complexity and priority
≥ 1 year of recent contribution to and accomplishment in all aspects of conducting clinical studies of standard complexity and priority (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities regulations and Novartis standards
Experience in managing people globally in a complex matrix environment preferred
Management of virtual teams. Proven ability and experience leading
Experience in developing effective working relationships with internal and external stakeholders
Good communicator and presenter (oral and written)
Good organization and prioritization
Negotiation and conflict resolution skills and enterprise mindset
Project management skills and demonstrated ability to meet timelines
Strategic thinking with analytical and problem-solving skills
Knowledge of appropriate therapeutic area preferred.
Skills Desired
Auditing, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Data Auditing, Data Management, Health Sciences, Lifesciences, Project Planning, Vendor Management, Waterfall Model