Programmer Analyst II

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

📋 Description

• Serve as the primary programmer, project lead, or oversight lead for various clinical-trial initiatives.

• Supervise statistical and bioinformatics programming from the planning phase to analysis and reporting.

• Coordinate teams and implement study strategies aimed at enhancing process and programming efficiencies.

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

• Represent the department both within the organization and during interactions with clients and regulatory bodies.

• Lead studies or drug programs of diverse complexity and scope.

• Conduct team meetings, create and manage project timelines, evaluate and forecast resources, and ensure compliance with study budgets and contractual commitments.

• Plan and contribute to tools and techniques that enhance process efficiencies, including leading solution teams.

• Represent the department during bid defenses and in clinical-data submissions or reviews with regulatory authorities.

• Act as the company's project manager for biometrics-only projects.

• Provide departmental infrastructure support, which includes conference representation, presentations, training materials, documents, policies, and initiatives.

• Enhance the knowledge of programming, clinical trials, and pharmaceutical industry developments for both personal and junior team members.

• Offer feedback on employee performance for development, evaluations, and training purposes.

• Promote the publication of industry articles and presentations at conferences.

• Participate in recruitment and candidate interviews.

⛳️ Requirements

• MS/MA degree in computer science, statistics, biostatistics, mathematics, or a related field with a minimum of 6 years of relevant experience; or a bachelor's degree in one of these disciplines or an equivalent formal academic/vocational qualification with at least 8 years of relevant experience.

• Equivalency may be considered through a combination of appropriate education, training, and/or directly related experience.

• Proficient SAS® programming skills.

• Strong comprehension of database structures and complex data frameworks.

• Exceptional attention to detail.

• Strong problem-solving abilities and innovative thinking.

• Excellent written and verbal communication skills, including proficiency in English.

• Capable of independently organizing, adapting, and adjusting to changing priorities across multiple tasks.

• Experience working and leading in a multidisciplinary team environment.

• Able to coach and mentor others through project leadership.

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

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

• Familiarity with clinical-data submission requirements for regulatory authorities.

• Strong project-management skills, including the creation and modification of project budgets, as well as management of project budgets and risks.

• Ability to interpret and contribute to company policies.

• Focused on delivery and quality.

• Occasional domestic and international travel may be required.

🏝️ Benefits

• Fully remote work arrangement.

• Training, guidance, and opportunities for professional development.

• Chance to represent the company at industry conferences.

• Opportunities to present and teach during department meetings.

• Global team collaboration.

• Reasonable accommodations for individuals with disabilities during hiring and employment.