Principal Clinical Programmer

🔥 1 minute ago

🇮🇳 India – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

👻 Ghost score 10%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Design, write, validate, and maintain clinical programming software using Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supporting tools • Generate and maintain documentation for specifications, programming, validation, annotated CRFs, databases, coding, edit checks, imports, exports, listings, and custom reports • Coordinate and lead development activities for clinical programming projects • Participate in project meetings, discussions, problem solving, and deliverable planning • Escalate issues affecting project dates, scope, or budget • Provide technology support to clinical programmers, Project Analysts, Data Managers, and other staff • Administer and provide technical support for core business applications and supplemental packages • Perform senior reviews of study-level, program-level, and multi-study deliverables • Attend sponsor audits and assist with in-progress audits • Review study budgets, monitor scope against actual work, and manage change orders • Monitor workflow alerts, system errors, and performance issues • Perform system integration, application updates, and user acceptance testing • Provide leadership, training, guidance, and support to department members • Collaborate with clients, peers, lead programmers, project teams, and requestors to finalize specifications • Lead assigned studies as the Clinical Programmer role at Quick Start Camps • Lead clinical programming activities on three to ten concurrent studies • Manage project resources and proactively communicate delivery and resourcing needs • Maintain current knowledge through literature, self-training, courses, and professional meetings

🎯 Requirements

• Experience and deep expertise in clinical programming and clinical data management • Proficiency with Medidata Rave, Oracle OC/RDC, Oracle Inform, SAS, and related supporting tools • Ability to design, write, validate, and maintain software according to specifications and standard development procedures • Experience developing specifications, programs, and validation documentation for annotated CRFs, database creation, coding configuration, edit checks, import/export processing, listings, and custom reports • Ability to coordinate and lead clinical programming project activities • Analytical problem-solving skills • Ability to manage multiple concurrent task assignments and studies • Ability to provide technology support and second-tier help desk support • Experience with application administration, system integration, application updates, and user acceptance testing • Ability to conduct senior review of study-level, program-level, and multi-study core deliverables • Ability to review study budgets, monitor scope of work, and manage change orders • Ability to provide leadership, training, guidance, and support to department members • Broad knowledge of clinical programming and clinical data management • Equivalent experience, skills, and/or education may be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations, when appropriate, for employees or applicants with disabilities