Seeking an associate director to join the Biostatistics department to manage, oversee and coordinate query work across multiple registries. This is a strategic as well as a technical position. This individual would need to learn the key themes and challenges for each of the registries and coordinate the workflow and assignment of the query work going forward. This person must have a successful track record of managing highly technical individuals and overseeing the execution of multiple projects. Requires strong knowledge of Biostatistical design. Must be a team player and leader. Must have the ability to see the big picture and future for query work.
The Associate Director will play a role in the following functional capacities:
Work with complicated longitudinal registry data to provide input and coordination of query work
Coordinate and facilitate discussion across biostatistical query leads in support of best practices
Identify best individual for each query to optimize work and facilitate biostatistical growth and development within the team
Facilitate and coordinate standardization of query work including automation of tables, as well as coordination and use of templates for SAPs/reports
Coordinate training program on relevant practices for query work with the goal of decreasing the time from day 1 to first query
EDUCATION & EXPERIENCE
Advanced degree (PhD or MS) in Biostatistics, Statistics or Mathematics or similar discipline required
Minimum of 8-10 years of post-doctorate experience in a research, medical or pharma setting
Knowledge of medical terminology and clinical epidemiology
Must be highly proficient in at least one of the following statistical packages: SAS, Stata or R/S-plus and ability to become proficient in others
Familiar with longitudinal data
Familiar with registry data
Proven ability to work independently with little supervision
Has extensive management experience including supervising individuals and has provided critiques of performance
Proven ability to gain consensus, make decisions and move projects forward
Ability to explain highly technical concepts to senior management
Remote position-must live in the USA
Must be able to remain in a stationary position 50%
[i]Disclaimer: This Job Description is subject to change at any time.
Telecommuting is allowed.
About Corrona LLC
Corrona provides real world evidence through syndicated registry data and analysis services, helping biopharmaceutical companies demonstrate the value of their products to clinicians, patients, payers, and regulators. Corrona operates six major autoimmune registries across the US, Canada and Japan, collecting data from over 500 participating investigator sites.
In addition, to supporting hundreds of manuscripts and abstracts, Corrona has supported post approval safety commitments for multiple advanced therapies approved for autoimmune conditions.
Corrona is headquartered in Waltham, MA. Through its subsidiary Health iQ, Corrona has access to a broad range of UK and international data sets across primary and secondary care, as well as deep relationships with the NHS, Public Health England, and leading UK academic institutions. The Company’s HealthiVibe business complements and strengthens Corrona’s strong presence in disease registries by providing market-leading expertise in supporting innovative, evidence-based patient engagement initiatives across the product lifecycle.