Senior Clinical Programmer I

At Allucent, you will be an integral part of a team 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. As a Senior Clinical Programmer I, your role will involve developing and coordinating clinical programming activities, maintaining clinical databases, and ensuring data processing in compliance with study-specific plans, standard operating procedures, industry standards, and regulatory requirements. You will provide expertise in relevant clinical programming areas and cross-functional initiatives, contributing to the development of departmental processes, tools, and staff training. Your key responsibilities will include: - Designing, building, testing, and releasing clinical databases to the production environment. - Developing and maintaining all clinical programming documentations to support implementation and ongoing data management activities. - Reviewing and providing input to study documentation, including Data Validation Plan, UAT Plan, test cases, and eCRF completion guidelines. - Programming electronic edit checks and data listings for data review and validation processes. - Developing and validating SAS programs for metric reporting, data import, reconciliation, and export set-up. - Leading and supporting the application of Clinical Data Interchange Standards Consortium (CDISC) conventions during database build activities and data warehousing. - Participating in study team meetings, contributing insights, and problem-solving analytically. - Collaborating with peers and study teams to clarify specifications and meet project needs. - Providing leadership, guidance, and support to junior programmers and department members. - Defining and promoting clinical programming best practices, training materials, and standard documents. - Leading development activities to standardize clinical programming procedures. - Maintaining knowledge in clinical programming and data management through continuous professional development. - Leading process improvement initiatives and supporting staff learning & development. - Representing the company at professional events and contributing as a Subject Matter Expert in Clinical Programming activities. To be successful in this role, you should have: - A degree in Life Science, Healthcare, Computer Science, or a related field. - Minimum 5 years of relevant work experience in drug development and/or clinical research. - Thorough knowledge of ICH-GCP(R2), GDPR/HIPPA, and applicable regulatory requirements. - Good understanding of CDISC standards, clinical data management processes, and electronic data capture systems. - Strong communication skills and the ability to work in a challenging environment. - Proficiency in programming languages such as PL/SQL, SAS, and Electronic Data Capture systems. - Strong technical, analytical, and problem-solving skills. Additionally, the benefits of working at Allucent include: - Comprehensive advantages package per location. - Competitive salaries per location. - Departmental Study/Training Budget for furthering professional development. - Flexible Working hours. - Leadership and mentoring opportunities. - Participation in the Buddy Program. - Internal growth opportunities and career progression. - Financially rewarding internal employee referral program. - Access to online soft-skills and technical training. - Eligibility for Spot Bonus Award Program and Loyalty Award Program. Please note that Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on open roles. Candidates should not be submitted directly to hiring managers, employees, or human resources. At Allucent, you will be an integral part of a team 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. As a Senior Clinical Programmer I, your role will involve developing and coordinating clinical programming activities, maintaining clinical databases, and ensuring data processing in compliance with study-specific plans, standard operating procedures, industry standards, and regulatory requirements. You will provide expertise in relevant clinical programming areas and cross-functional initiatives, contributing to the development of departmental processes, tools, and staff training. Your key responsibilities will include: - Designing, building, testing, and releasing clinical databases to the production environment. - Developing and maintaining all clinical programming documentations to support implementation and ongoing data management activities. - Reviewing and providing input to study documentation, including Data Validation Plan, UAT Plan, test cases, and eCRF completion guidelines. - Programming electronic edit checks and data listings for