Manager, CSAR - SAS Edit Check Programmer

Manager, CSAR - SAS Edit Check Programmer

Roles & Responsibilities

• SAS Edit Check Programming:

  Create and program complex

  SAS

  edit checks according to specifications, testing them for functionality and identifying potential issues before implementation.

• Technical Leadership & Collaboration:

  Act as a technical point of contact for systems deliverables and provide programming support to Clinical Study Teams. You will work collaboratively with Clinical Data Management to meet study deliverables and timelines.

• Data & Systems Support:

  Support clinical trial platform technologies and provide technical and business process input on new and emerging technologies. You will also act as a data scientist, bringing awareness to patterns and analytical insights to support decision-making.

• Quality & Compliance:

  Develop, review, and implement policies,

  SOPs

  , and associated documents. You will assist in preparing for and responding to audit findings, both internal and external.

• Project Management:

  Contribute to large system transformation projects, with a focus on project management, stakeholder engagement, and change management.

Technical Skills & Knowledge

• Proficient in

  SAS

  edit check programming.
• Operational experience with clinical database management systems and allied technologies (e.g.,

  Rave EDC, Veeva EDC

  ).
• Strong understanding of

  Good Clinical Practice

  , drug development, and clinical trials processes.
• Knowledge of systems development lifecycle, data management processes, and programming of clinical trial databases.
• Expertise in performance management techniques, problem-solving, and analytical thinking.
• Experience with project planning and management.
• Experience with quality management, risk analysis, and process improvement methodologies.

Qualifications

• A Bachelor's degree or equivalent in life science, computer science, business administration, or a related field, or a Master's degree.
• Broad knowledge and experience in data management/programming in the Pharmaceutical or Biotech industry.
• General biopharmaceutical clinical research experience is preferred.
• Experience in oversight of outside vendors (

  CROs

  , central labs, etc.) is a plus.

Soft Skills

• Leadership:

  A strong leader with a demonstrated ability to influence stakeholders and mentor others.

• Problem-Solving:

  Excellent analytical and problem-solving skills, with a focus on using data to drive decisions.

• Communication:

  Strong verbal and written communication skills, with the ability to collaborate effectively with global, cross-functional teams.

• Proactiveness:

  High degree of initiative and self-motivation, with the ability to manage multiple priorities successfully.

• Teamwork:

  Team-oriented, with a focus on achieving team goals.