Statistical Programmer I

October 9

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Logo of Altasciences

Altasciences

Clinical Research • Clinical Trials • Phase I-II • Human Abuse Liability & Abuse Potential • Early Cardiac Safety & TQT

1001 - 5000

💰 Private Equity Round on 2017-06

Description

• The Statistical Programmer I is responsible for developing high-quality programming that support sponsors’ research programs • Follow the department and company standard operating procedures (SOPs), policies, and standards • Using SAS, perform SDTM, ADaM, and table, figure, and listing (TFL) programming, quality control (QC) review, and documentation of programs used in creating statistical outputs • Understand regulatory agency standards and provide final deliverables in accordance with these standards • Collaborate with Lead Biostatisticians to resolve any study-related questions • Perform peer review and take accountability for ensuring programming accurately reflects the raw data • Follow current SDTM standards and current ADaM Implementation Guides • Lead studies or portions of studies from a programming perspective • Perform review of the clinical database in regards to visit naming, Clinical Data Acquisition Standards Harmonization (CDASH) • Create Biostatistics deliverables that follow the protocol and SAP • Accurately import external data to be used in TFLs • Interact with other staff members to understand and explain SAS programs accurately • Analyze existing processes and explore improvement solutions • Provide technical expertise for internal and external clients

Requirements

• Bachelor's Degree in programming, health-related sciences, or relevant field • 1 to 3 years experience in the field • Excellent verbal and written communication skills • Professional attitude and strong interpersonal skills • Ability to work well with a multi-disciplinary team of professionals • Client-focused approach to work • Flexible attitude with respect to work assignments and new learning • Ability to prioritize workload • Superior attention to detail • Understanding of clinical research and the relationship of Data Management in the clinical study process • Strong technical aptitude and ability to adapt to multiple data management platforms • Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to multiple information technology (IT) systems

Benefits

• Health/Dental/Vision Insurance Plans • RRSP with Employer Match • Paid Vacation and Holidays • Paid Sick and Bereavement Leave • Employee Assistance & Telehealth Programs • Training & Development Programs • Employee Referral Bonus Program • Annual Performance Reviews

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