
Data Science Program Lead I
Posted 17 hours ago

Posted 17 hours ago
• Aligns DSS study teams with both program- and study-level strategies.
• Leads the DSS Study Team for assigned studies and serves as a representative of DS within the cross-functional study team.
• Acts as the primary point of contact and is the accountable operational lead from DSS for designated studies.
• Coordinates related DSS study teams to achieve operational goals.
• Engages and connects global functional and cross-functional teams.
• Interacts with and influences cross-functional team members to meet program and study objectives.
• Utilizes operational analytics and project management tools to enhance the execution of programs and studies.
• Anticipates and identifies potential issues that may impact timelines or quality and devises options and solutions.
• Ensures compliance with federal regulations, relevant local regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs).
• Keeps updated on new and/or evolving local regulations, guidelines, and policies pertaining to clinical development.
• Participates in the oversight of vendors and offers feedback regarding study operations, issues, and performance trends.
• Responsible for coaching and mentoring Data Science Associates.
• May involve indirect supervision of tasks performed by contract resources.
• Engages in DSS and cross-functional innovation and process improvement initiatives.
• Contributes to documenting 'lessons learned' from study execution across different functions.
• Bachelor’s degree in business, management information systems, computer science, life sciences, or a related field.
• Master’s degree is preferred.
• PMP Certification or Lean Six Sigma Green Belt is desired.
• A minimum of 3+ years of experience in pharma, clinical research, data management, or healthcare, or 5+ years of project management experience (or relevant work experience).
• Strong understanding of the clinical trial process and clinical technology.
• Preferred experience in managing a clinical trial from initiation to completion.
• Proven effective leadership abilities.
• Demonstrated capability to influence others without direct authority.
• Strong effective communication skills.
• Proven effective analytical skills.
• Paid time off (vacation, holidays, sick leave).
• Medical, dental, and vision insurance.
• 401(k) plan available to eligible employees.
• Short-term incentive programs.
InPost Group
Syneos Health
Clinical Outcomes Solutions
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