Programmer Analyst II

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

📋 Description

• Act as the primary programmer or project leader for studies or drug programs with diverse complexity and scale.

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

• Conduct meetings with project leaders and client representatives.

• Create and maintain project timelines, evaluate and predict resource needs, and ensure compliance with study budgets and contractual agreements.

• Strategize and implement enhancements to tools and techniques that boost process efficiency.

• Lead solution teams and engage in initiatives aimed at process and tool enhancements.

• Act as the department representative to clients regarding study-related matters, bid defenses, and submissions or reviews of clinical data with regulatory bodies.

• Directly contribute to proposals and bids.

• Serve as the company project manager for biometrics-only projects when applicable.

• Provide infrastructure support, represent at conferences, deliver departmental presentations, and create teaching materials, documents, policies, and departmental initiatives.

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

• Provide managerial feedback regarding employee performance, development, evaluations, and training.

• Promote the publication of articles and presentations at conferences to elevate the company's visibility.

• Assist in recruitment and conducting candidate interviews.

⛳️ 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.

• Consideration may be given for equivalency through a combination of relevant education, training, and/or related experience.

• Proficient in SAS® programming.

• Strong grasp of database structures and complex data frameworks.

• Meticulous attention to detail.

• Possess problem-solving and innovative capabilities.

• Outstanding written and verbal communication skills.

• Proficient in English language.

• Ability to organize, adapt, and respond to shifting priorities across various assignments.

• Capability to work and lead within a multidisciplinary team environment.

• Familiarity with clinical trials, ICH Statistical and reporting guidelines, and GCP.

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

• Awareness of clinical data submission requirements for regulatory authorities.

• Proficient project management skills, including the creation, updating, and management of project budgets and associated risks.

• Ability to interpret and contribute to company policies.

• Driven by delivery and quality standards.

🏝️ Benefits

• Opportunities for collaboration and professional development.

• A global team environment.

• A culture of passion, innovation, and dedication to scientific excellence.