Qualifications
• Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Req
• Master's Degree Master's Degree in life sciences related discipline or related field
Pref
• Ph.D. Ph.D. in life sciences related discipline or related field Pref
• Typically requires at least 3 years of prior relevant experience and related competency levels. Req
• Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents. Req
• Ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Req
• Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
Req
• Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output. Req
• Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. Req
• Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues. Req
• In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. Req
• Excellent written and oral communication skills including grammatical/technical writing skills.
• Excellent attention to detail and accuracy.
• Communicates clearly, effectively and confidently with others.
• Demonstrated abilities in collaboration with others and independent thought.
• Demonstrates confidence and maturity in most routine medical writing situations.
• Demonstrates good judgement in requesting input from senior staff.
• Ability to establish and maintain effective working relationships with coworkers, managers and customers.
• Ability to effectively manage multiple tasks and projects.
• Ability to proactively identify potential issues/risks, consider solutions, and raise with the customer, with senior guidance and input.
• Must be computer literate.
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