Note: The job is a remote job and is open to candidates in USA. Syneos Health is a fully integrated life sciences services organization supporting drug development and commercialization. The Principal Clinical Programmer leads clinical programming activities across individual studies and large study programs, designing, validating, and maintaining applications for clinical data capture and processing while providing technical expertise, project oversight, mentorship, and vendor management.
Responsibilities
- Must have experience in Rave Programming, Custom Functions Programming (Moderate to Complex) with minimum 2+ years in CF. Overall 10+ years of experience is required
- Must have Migration exposure, Publish Check, PPC, TSDV, Study Build programing, SDBE Rave certification mandatory
- Preferred Veeva CDMS experience
- Provides application administration and technical support as the subject matter expert on all core business packages, including but not limited to: Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supplemental packages such as migration mentoring/review, reporting tools, custom functions, etc. Utilizes primary development tools and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures
- Generates and maintains all required documentation including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRF)s, database creation, coding setup, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports
- Monitors applications proactively for workflow alerts, system errors, performance issues and troubleshoot programming deliverable defects
- Performs system integrations activities, application updates, and user acceptance testing
- Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources
- Participates in and provides input at project review and departmental review meetings. Participates in bid defenses
- Ensures high quality deliverables by providing senior review of ’program level’/multi-study core deliveries for accuracy. Attends sponsor audits and assists with in-progress audits
- Reviews and provides input on study budgets, manages project level metrics, progress, and status, for large programs of studies from key sponsors. Monitors scope of work to actual work, alerting management of potential change orders; manages and executes the change order to completion. Assists with the creation of change orders
- Provides leadership, mentorship, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams and/or requestors to clarify and finalize specifications and uses expanded technical skills to meet evolving project needs
- Attends Quick Start Camps (QSCs) in the lead Clinical Programmer role for assigned studies
- Provides leadership/oversight of five (5) to twenty (20) concurrent studies depending upon scope, similarity, program, and resourcing requirements. This may include the oversight of other lead programmers and their associated studies
- Manages project resources, proactively alerting management of delivery and resourcing needs
- Assists with management of application vendors and serves as an initial escalation contact. Monitors vendor service level agreements (SLAs) and reports metrics to upper management
- Supervises the implementations of upgrades and new modules of remotely hosted vendors, acquiring all documentation and storing in the relevant areas
- Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc
- Contributes towards the update of standard operating procedures and work instructions in line with department and company process and policy
- As required, oversees program level clinical programming operations by providing supervision for a team of clinical programmers. Responsibilities may include professional development performance appraisals, and employee advising for junior staff. Assigns project work and reviews workload for all direct reports. Manages staff development by establishing goals that will increase knowledge and skill levels and by delegating tasks commensurate with skill level. Resolves conflicts/priorities at the program level prior to making any recommendations to management. Advises on administrative policies and procedures, technical problems, priorities, and methods
Skills
- Must have experience in Rave Programming, Custom Functions Programming (Moderate to Complex) with minimum 2+ years in CF
- Overall 10+ years of experience is required
- Must have Migration exposure, Publish Check, PPC, TSDV, Study Build programing, SDBE Rave certification mandatory
- Preferred Veeva CDMS experience
Benefits
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Inclusive culture where employees can authentically be themselves
Company Overview
Company H1B Sponsorship