Programmer Analyst II

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

📋 Description

• Act as the primary programmer, project lead, or oversight lead for multiple clinical trial or drug program initiatives.

• Supervise statistical and bioinformatics programming from the study design stage through 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.

• Collaborate with project leaders and client representatives to facilitate meetings, manage timelines, forecast resources, and ensure adherence to budget and contractual obligations.

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

• Serve as the company project manager on projects focused solely on biometrics services when applicable.

• Provide departmental infrastructure support, including training materials, documents, policies, and initiatives for process improvement.

• Enhance the knowledge and professional skills of oneself and junior team members.

• Offer performance feedback for employee development, reviews, and training sessions.

• Increase the company's visibility through industry publications and presentations at conferences.

• Participate in recruitment efforts 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 or equivalent/relevant formal academic or vocational qualification with at least 8 years of relevant experience.

• A combination of appropriate education, training, and/or directly related experience may be considered as an equivalency.

• Proficient in SAS® programming.

• Strong understanding of database structures and complex data architectures.

• Exceptional attention to detail.

• Excellent problem-solving and innovative abilities.

• Outstanding written and verbal communication skills.

• Proficient in the English language.

• Capable of independently organizing, adapting, and adjusting to shifting priorities across multiple assignments.

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

• Positive demeanor with a strong capacity to collaborate with others.

• Ability to coach and mentor colleagues, demonstrated through project leadership experience.

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

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

• Good grasp of clinical data submission requirements for regulatory authorities.

• Strong project management capabilities, including budget creation, updates, and management of budgets and risks.

• Ability to interpret and contribute to company policies.

• Commitment to delivery and quality.

• Willingness to travel occasionally, including domestic and international travel, and make occasional drives to site locations.

🏝️ Benefits

• Training, mentorship, and opportunities for project leadership.

• Professional development and enhanced knowledge of programming technology, clinical trials, and advancements in the pharmaceutical industry.

• Opportunity to represent the company at industry conferences.

• Opportunities to publish articles in industry journals and present at conferences.

• Collaboration and development as part of a global team.

• Reasonable accommodations for individuals with disabilities.

• Employment consideration without regard to protected characteristics in accordance with the company's Equal Opportunity Employer policy.