Clinical Science SAS Programmer

il y a 2 semaines

Bruxelles, Région de Bruxelles, Belgique Precision for Medicine Temps plein
Precision for Medicine is not your typical CRO.

At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.

What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.

As our organisation continues to grow we are hiring a Clinical Science SAS Programmer.

Job Summary

  • Focused on developing and maintaining SAS programming to support the review of clinical data as part of the integrated crossfunctional data cleaning approach
  • Contributes to the development and enhancement of programming standards to ensure efficiency and consistency across projects
  • Requires a working understanding of oncology clinical research and the drug development process
  • Requires the ability to work as part of a crossfunctional team to ensure the development and implementation of process consistent with Precision for Medicine's values and overall focus as it relates to quality
  • Requires strong interpersonal, organizational and communication skills to ensure the ability to set and achieve objectives
  • Collaborates internally and with other departments (clinical, project management, data management, safety, translational science, vendors, etc.) to achieve objectives
  • Provides high quality and timely deliverables that require an understanding of functional and crossfunctional relationships
  • Supports continuous process improvement to further departmental and company objectives and build/preserve the company's quality reputation and image
  • Expected to be able to work remotely with mínimal supervision
  • Performs other duties as assigned by management

Job Duties and Responsibilities:

  • Focused on developing and maintaining programming via SAS to support CSAI-OS review of clinical data as part of the integrated crossfunction data cleaning approach (e.g., Patient Profiles, Excel workbooks, metrics, data visualization)
  • Runs SAS programs and provides outputs at study defined frequencies to internal and external team members/study drives.
  • Supports the development and maintenance of a central SAS macro library within CSAI-OS
  • Develops and maintains a good working relationship with internal and external project team members, serving as an ambassador to promote Precision's high quality and ethical image in accordance with the company Core Values.
  • Supports the identification of quality risks and issues
  • Participates as needed in internal and external studyspecific team meetings
  • Independently and consistently enact and share best practices within CSAI-OS programming
  • Participates in the interview process for new CSAI-OS employees by conducting CV review and participating in interviews.
  • Performs other duties as assigned by management

Minimum Requirements:

  • Bachelor's degree required
  • Minimum of five (5) years or eight (8) years (Sr. level) of experience in clinically based programming within either the CRO or pharmaceutical industry
  • Excellent understanding of and experience with: SAS Base, SAS macro facility, database design principles, general statistical concepts and procedures
  • Oncology experience preferred
  • Experience with electronic data capture systems (EDC, such as RAVE, Medrio, DataTrak)
  • Experience with data visualization tools (such as JReview)
  • Experience producing output to various destinations (Word, Excel, Adobe)

Key Competencies:

  • Advanced SAS clinical programming experience (oncology preferred)
  • Advanced computer skills
  • Team oriented; good written and verbal communication skills
  • Working knowledge of ICH-GCP, relevant SOPs and regulatory guidance with ability to operationalize and implement
  • Wellrounded knowledge of entire clinical trial process and working understanding of the role of each department
  • Ability to work in a crossfunctional environment
  • Ability to develop and maintain effective working relationships
  • Demonstrates flexibility and cooperation
  • Ability to plan, organize, delegate, influence and make decisions using critical thinking and problemsolving skills
  • Solid time management, negotiation and conflict management skills.
  • Ability to manage and support change
  • High level of integrity with ability to inspire the highest standards from a professional and ethical perspective.
  • Understanding of cultural aspects relevant to working in a global environment
  • Ability to read, write and speak fluent English
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law Precision Medicine Group, LLC

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