Programmer Analyst II

This is a fully remote position, open to applicants in China.

📋 Description

• Act as the primary programmer, project leader, or oversight lead for studies and drug programs with varying degrees of complexity and scale.

• Supervise statistical and bioinformatics programming for clinical trials from the design phase through analysis and reporting.

• Coordinate teams and implement study strategies to enhance process and programming efficiencies.

• Develop and uphold programs for generating statistical reports and validating programs.

• Facilitate team meetings with project leaders and client representatives.

• Create and manage project timelines, evaluate and forecast resources, and ensure compliance with study budgets and contractual obligations.

• Plan and contribute to tools, techniques, process efficiencies, solution teams, proposals, bids, and regulatory submissions or reviews.

• Offer infrastructure support, represent at conferences, create presentations, training materials, department documents, policies, and initiatives for process improvement.

• Enhance knowledge and professional skills for oneself and junior team members.

• Deliver performance feedback for employee development, reviews, and training.

• Promote the publication of industry articles and conference presentations.

• Assist in recruitment and candidate interviews.

• Provide project leadership and act as a representative of the department to clients and regulatory agencies.

⛳️ Requirements

• MS/MA degree in computer science, statistics, biostatistics, mathematics, or a related field with a minimum of 6 years of experience, or a Bachelor's degree in a related field or equivalent with at least 8 years of experience.

• An equivalency of appropriate education, training, and/or directly related experience may be considered.

• Proficient in SAS® programming.

• Strong understanding of database structures and complex data systems.

• Exceptional problem-solving and innovative abilities.

• Outstanding written and verbal communication skills.

• Proficiency in the English language.

• Capability to organize, adapt, and adjust to changing priorities across multiple assignments.

• Ability to work and lead in a multidisciplinary team environment.

• Skills to coach and mentor others.

• Understanding of clinical trials, ICH statistical and reporting guidelines, and GCP.

• Comprehensive knowledge of statistical principles applied to clinical trial design and analysis.

• Familiarity with clinical data submission requirements for regulatory authorities.

• Excellent project management skills, including project budget creation, updates, and budget and risk management.

• Ability to interpret and contribute to company policies.

• Results-oriented and quality-focused.

• Willingness to travel domestically and internationally on occasion.

🏝️ Benefits

• Collaboration and development integrated into everyday experiences.

• Reasonable accommodations provided for individuals with disabilities.

• Commitment to equal opportunity employment.