Clinical Programming Manager

ICONMA, LLC • United States, United States • 9h ago

Our Client, a Pharmaceutical company, is looking for a Clinical Programming Manager for their Remote location. Responsibilities:

The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials.

The Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources. The role may require providing input to design and analysis, and report the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.

Provides input for Budget Planning

Likely to oversee contingent workers and/or vendors; Likely to provide training to others

Primarily works at the project level

Delivers assignments with quality and within timelines

Contributes strategy under moderate supervision

Provides strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets

Has good knowledge and understanding of the statistical models in efficacy data analysis

Responsible for the standardization of Clinical Programming deliverables within a project

Extends existing or develops new clinical programming methods to solve complex problems

Requirements:

Bachelor's Degree/ Master's Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

Bachelor's + 5 years or Master's + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer

Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.

Advanced level of SAS programming skills. Develop SAS programs and perform QC tasks for integrated analysis.

Intermediate knowledge of government regulations pertaining to drug development in multiple therapeutic areas.

Contributes to strategy under moderate supervision

Tackles difficult problems; identifies solutions and recommends action to management

Influences communication toward common understanding and actionable results; contributes to process and development

Ability to effectively work in a global environment

Ability to effectively interact with and influence others without direct reporting relationships.

Why Should You Apply?

Health Benefits

Referral Program

Excellent growth and advancement opportunities

As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.

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