Clinical Programmer Analyst

3 weeks ago

Nutley, United States Tech Observer Full time

Job Title: Clinical Programmer Analyst (Rave) - Senior

Location: Fully Remote

Duration: 12 months contract with possible more extension


W2 Profiles only no C2C.


Primary responsibilities

100% Remote

Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE

Strong Programming skill set

Knowledge of Python, building dashboards

Knowledge of API programming

Demonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisions

Demonstrated skill in leading teams, by example and mentoring staff

Excellent oral and written communication and presentation skills

Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC. Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies

Demonstrated ability to work in a team environment

Demonstrated ability to handle multiple competing priorities

Proven interpersonal skills


Responsibilities

Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave

Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles.

Provide technical support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modules

Serve as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.

Create Advanced Analytics dashboards

Insights into creating actionable dashboards and deep understanding and knowledge of good interpretation of clinical data

Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency

Responsible for conducting Quality Control of study design for assigned projects and participate in the validation of EDC studies

Responsible for the creation and maintenance of library objects within the Global Libraries

Responsible for ensuring compliance of standard objects usage throughout the business

Responsible for the management of standard objects within the Global Libraries

Perform all activities related to specification development for study build and design of databases according to Standard procedures

Responsible for the review and approval of derivations and edit checks requested by the project teams

Participate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activities

Complete work according to company SOPs, Work Instructions and project specific guidelines in accordance with Good Clinical Practice

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