Senior Clinical Analyst, Programmer

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

📋 Description

• Oversee programming efforts for data listings, Safety Review Listings, Centralized Monitoring Listings, and various reports.

• Collect, comprehend, and assess requirements from the Data Management and Risk-Based Study Management departments.

• Develop code to fulfill departmental requirements within established timelines and budget constraints.

• Formulate listing specifications based on user needs, primarily from DM and RBSM.

• Generate SAS Data Review Listings in accordance with the protocol, EDC Database, and Data Validation Specifications.

• Establish and maintain a repository of Manual Data Review Listings.

• Produce Safety Review Listings.

• Engage in the creation of reports and listings that support Centralized Monitoring activities.

• Record modifications to code and specifications.

• Aid in the development of SOPs related to the enforcement of data standards.

• Contribute to strategies aimed at enhancing productivity and quality while reducing cycle times and costs.

• Guide junior Analysts and Programmers.

• Execute tasks in accordance with regulatory requirements, industry standards, SOPs, sponsor specifications, and timelines.

⛳️ Requirements

• A Bachelor of Science degree is mandatory.

• A minimum of 10 years of clinical research experience in the biotechnology, pharmaceutical, or CRO sectors, with at least 5 years in SAS programming.

• In-depth understanding of regulatory requirements and the drug development lifecycle.

• Extensive familiarity with clinical trial data, SAS data, and database specifications.

• Exceptional verbal and written communication skills in English.

• Capability to thrive in a fast-paced environment, demonstrating agility in managing and prioritizing multiple competing tasks.

• SAS certification and/or Advanced Programmer experience would be beneficial.

• Highly organized and detail-oriented, with strong project planning and time management abilities.

• Must have legal authorization to work in Argentina.

🏝️ Benefits

• Flexible work schedule.

• Permanent full-time position.

• Continuous learning and development opportunities.

• Attractive opportunities for advancement.

• Equal opportunity and accommodations available throughout the recruitment and selection process, upon request.