Arrowhead Pharmaceuticals, Inc. Pasadena , CA 91101
Posted 2 weeks ago
The Position
We are seeking a manager for clinical programming to join our growing biometrics team to support clinical studies across Arrowhead's expanding portfolio. This is an exciting opportunity for a candidate trained in SAS programming and data analysis is who has some prior experience working as a clinical or statistical programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or statistical programming, with a goal to develop as a lead within clinical programming.
Responsibilities
Develop, and execute edit checks and patient profile software or programs for clinical trials
Develop and execute data listing programs used by data managers, safety surveillance, medical or clinical operations personnel
Collaborate with data management to ensure appropriate data collection and reporting
Participate in study team meeting and support data management activities
Program and deliver results on time for ad-hoc data programming requests
Define and help implement statistical computing environment, specifically SAS server setup and work practices
Support statistical programming, from raw data to ADaM, of efficacy and safety evaluation
Interface with CRO and perform quality audits on CRO outputs; review outputs provided by CROs for accuracy and consistency with the programming specs
Assist in efforts to identify, develop, and implement departmental standards, applications, processes and training
Develop or support standard operation procedure preparation
Requirements:
Bachelor's degree in life sciences or technical field
At least 3 years' experience of SAS programming for clinical trials for Manager; at least 5 years' experience Sr. Manager
Working knowledge of SAS, including complex data manipulation, data presentation and output deliver systems
Prior experience implementing edit checks and patient profiles on active clinical trials
Excellent verbal and written communication skills
Preferred:
Familiarity with CDISC standards, derivation of SDTM and ADaM specifications
Data management experience
Proficiency in R
CRO experience
Arrowhead Pharmaceuticals, Inc.