
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.
🔥 0 minutes ago
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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.
• Provide application administration and technical support as a subject matter expert for Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, migration tools, reporting tools, and custom functions • Design, write, validate, and maintain software according to specifications and standard development procedures • Create and maintain documentation for annotated CRFs, database creation, coding setup, edit checks, imports, exports, listings, and custom reports • Monitor applications for workflow alerts, system errors, performance issues, and programming defects • Perform system integrations, application updates, and user acceptance testing • Lead development activities for clinical programming projects and communicate risks affecting dates, scope, or budget • Participate in project, departmental, and bid defense meetings • Provide senior review of program-level and multi-study core deliverables • Attend sponsor audits and assist with in-progress audits • Review study budgets and manage program metrics, progress, status, scope, and change orders • Mentor, train, guide, and support department members • Attend Quick Start Camps as lead Clinical Programmer • Provide leadership and oversight for five to twenty concurrent studies • Manage project resources and vendor relationships, including SLAs • Oversee upgrades and new module implementations for remotely hosted vendors • Update standard operating procedures and work instructions • Supervise clinical programming operations and staff development as required
• Experience in Rave Programming • Custom Functions Programming (Moderate to Complex) • Minimum 2+ years in Custom Functions (CF) • Overall 5–7+ years of experience • Migration exposure • Publish Check, PPC, and TSDV experience • Study Build programming experience • SDBE Rave certification mandatory • Preferred Veeva CDMS experience • Broad knowledge of clinical programming and clinical data management • Ability to design, write, validate, and maintain software • Ability to generate and maintain required technical and validation documentation • Ability to perform system integrations, application updates, and user acceptance testing • Ability to lead clinical programming project activities and oversee concurrent studies • Ability to manage project resources, metrics, budgets, scope, and change orders • Ability to provide leadership, mentorship, training, guidance, and supervision • Ability to manage application vendors and monitor SLAs
• 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
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