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  • Lead Statistical Programmer

    4 days ago

    Emelle, Alabama, United States Pharmaceutical Research Associates, Inc Full time

    Overview:Joining Pharmaceutical Research Associates, Inc. is more than just a career; it’s a commitment to enhancing the lives of patients through innovative research. Transitioning to a new role can be a significant decision, and we understand the importance of this choice. At Pharmaceutical Research Associates, Inc., we value our employees as the...

  • Senior Clinical Study Lead

    2 weeks ago

    Emelle, United States Pharmaceutical Research Associates, Inc. Full time

    Overview: As a Sr. Clinical Study Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities: What you will be doing: Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as...

  • Lead Clinical Study Manager

    4 days ago

    Emelle, Alabama, United States Pharmaceutical Research Associates, Inc. Full time

    Overview:As a Senior Clinical Study Lead, you will be a key player in one of the most extensive and innovative clinical research organizations, driven by healthcare insights.Key Responsibilities:Your Role:Directs the interdisciplinary study team accountable for the execution of clinical studies and serves as the main liaison for oversight and leadership for...

Senior Statistical Programmer

2 months ago

Emelle, United States Pharmaceutical Research Associates, Inc. Full time

Overview:

As a Senior Statistical Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Responsibilities:

Create standard reports in different output formats. Automate programming tasks within the SAS environment. Generate programmed QC checks. Build utilities in support of other programming tasks. Design new tools or review existing tools and improve where needed. Develop, validate and document programs for ad-hoc analyses. Assess the time needed to develop programs and can at least partially self-manage the work. Take responsibility to deliver a support in time in function of stakeholders needs. Qualifications:

Able to lead studies under supervision. Able to demonstrate strong programming and domain expertise. Able to execute a wide range of programming activities with minimal supervision. Able to identify gaps in current programming best practices and offer suggestions for improvement. Minimum 5 years' experience within Statistical Programming in a clinical environment.

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