Clinical Programmer II (India)

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for Clinical Programmer II to join our A-team (hybrid*). As a Clinical Programmer II at Allucent, you are responsible for leading and coordinating clinical programming activities and maintaining clinical databases and other application tools supporting data capture and data processing in compliance with study-specific plans, standard operating procedures, industry standards and regulatory requirements.

In this role your key tasks will include:

• Design, build, test and release clinical databases to the production environment ·
• Develop and maintain all clinical programming documentation in support of implementation and ongoing data management activities. ·
• Review and provide input to study documentation including Data Validation Plan, UAT Plan, test cases and eCRF completion guidelines ·
• Program electronic edit checks and data listings required for data review and validation process ·
• Develop and/or validate SAS programs for metric reporting, data import, data reconciliation and data export set-up ·
• Support application of Clinical Data Interchange Standards Consortium (CDISC) conventions during database build activities, i.e. CDASH ·
• Review and adhere to the requirements of study-specific data management documents & plans ·
• Develop and lead clinical programming activities for assigned studies (including monitoring of project timelines, scope of work, budgets, resourcing needs and escalating potential problems effectively and promptly) ·
• Participates in/contributes to study team meetings and departmental meetings, uses an analytical approach to providing input and problem solving ·
• Collaborates with peers, leads programmers and study teams to clarify specifications and uses expanded technical skills to meet evolving project needs ·
• Understands validation principles and consistently develops code by those requirements ·
• Comply with clinical programming best practices, global libraries and standards ·
• Assist in standardizing data management procedures such as documentation for departmental operating procedures ·
• Develop and maintain a broad overall knowledge of the field of clinical programming and clinical data management by reading
• literature, self-training, continuous professional development, attending training classes and professional meetings etc. ·
• Propose and support initiatives for improving efficiency