Principal Clinical Programmer - Remote / Telecommute

Irvine, CA, US • Posted 17 hours ago • Updated 17 hours ago

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Job Details

Skills

Business Objects
C#
Clinical Data Management
Clinical Research
Clinical Trials
Collaboration
Communication

Summary

We are looking for Principal Clinical Programmer - Remote / Telecommute for our client in Irvine, CA

Job Title: Principal Clinical Programmer - Remote / Telecommute

Job Location: Irvine, CA

Job Type: Contract

Job Overview:

Pay Range: $56.31hr - $64.88hr

Responsibilities:

Provide technical expertise in clinical programming functional area and lead in the development of clinical databases. Development includes tools and programs for data validation checks, custom functions (C#) and clinical trial reporting in collaboration with key stakeholders.
Lead cross functional teams in the design and delivery of complex functional modules (e.g. TSDV, BO4 etc.) and provide clinical programming expertise regarding clinical trials, protocols, and case report forms.
Lead the development of specifications for systems and/or processes, system upgrades/enhancements and integration; and engage IT to deliver higher level support to users.
Develop and present high level technical training to end-users, including providing guidance to lower-level Clinical Programmers in their training program development.

Qualifications:

Bachelor's Degree or higher related field with 8-10 years of previous related experience in clinical research database programming, data management, software programming or related field or equivalent work experience based on the client criteria Required or.
Deep subject matter expertise in Medidata EDC including C# custom function development.
Proven successful project management skills.
Proven expertise in both Microsoft Office Suite, including advanced Excel and CDM (Clinical Data Management) systems.
Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives.
Good presentation and facilitation skills.
Ability to translate technical information to cross-functional teams.

Soft Skills:

Strong team orientation with the ability to collaborate effectively across cross-functional clinical teams.
Willingness to balance high-level technical work with detailed documentation and administrative responsibilities.
Ability to work with a sense of urgency and contribute quickly in a fast-paced environment.
Clear and proactive communication, especially when working with distributed teams.

Top Priorities for Success in Role:

Candidates must demonstrate hands-on experience in the following areas:
Medidata Rave (Metadata) New Study Builds (required).
TSDV (Targeted Source Data Verification module).
Custom Functions (must have hands-on development experience).
Advanced Edit Checks/Data Validation Logic.
Candidates without direct experience in these areas, particularly custom function development within Medidata, will not be considered for this level.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10516350
Position Id: CA_PCRT_0324
Posted 17 hours ago

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