Principal Programmer - RAVE (UK or EU)

Temps complet | Eu, HAUTE NORMANDIE | 7 mois | Date limite: 14 octobre 2018 00h 00min 00s
Cette position a expiré. Ne pas appliquer!

Résumé de l'emploi

Temps complet
; Competitive
Syneos Health

Description de poste

Job Details
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Job 347 of 1000
Principal Programmer - RAVE (UK or EU)

Company: Syneos Health
Location: UK or EU
Reference: 18005816
Closing Date: 14 Oct 18
Type: Full Time
Salary (£): Competitive

Job Summary:

Here at Syneos Health we are looking for Database programmer who is an expert in RAVE programming. If you are looking for your next challenge or a step up in your career please apply or get in touch.


Serves as lead Clinical Programmer to manage and support all functional tasks and project deliverables from single study assignments to large programs of studies.  Manages multiple project timelines, deliverables, while leading less experienced programmers.  Designs, writes, validates, and maintains software to meet specifications.  Specifies, develops, and validates applications supporting data capture and processing.  As senior technical subject matter expert, supports clinical programming and Data Management staff for Electronic Data Capture (EDC), reporting, and processing tools.  Proactively monitors internally and externally hosted applications for performance and/or system errors.  Supports projects and applications externally.  Manages external application vendor issues, integrations, and implementations.  May have supervisory  responsibility and/or oversight for a team of lead clinical programmers within a program.

Essential Functions:

Provides application administration and technical support as the subject matter expert on all core business packages, including but not limited to:  PF Inform, MDSOL Rave, Oracle RDC, NGC CRF W/M, 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 profile reporting.

Monitors applications proactively for workflow alerts, system errors, and performance issues.

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 criticism.  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.

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.

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.

Other Responsibilities:

Performs other work-related duties as assigned.    Minimal travel may be required (up to 25%).   Travel may be required for sales presentations and to address project-specific needs; however, this will not be a significant part of the position.

Contact Information:

Address:  European Head Office
1 Pinehurst Road, Farnborough, Hants
GU14 7BF
Tel:  +44 (0) 1189 335 300
Website:  Visit Our Web Site

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