Senior Clinical Analyst, Programmer

Job not on LinkedIn

🔥 12 hours ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

💊 Pharmaceuticals

🏥 Healthcare

💼 Consulting

Pharmaceuticals • Healthcare • Consulting

Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.

📋 Description

• Lead programming activities for data listings, Safety Review Listings, Centralized Monitoring Listings, and reports • Gather, understand, and analyze needs from Data Management and Risk Based Study Management departments • Create code to address departmental needs within agreed timelines and budget • Create listing specifications based on user requirements, mainly from DM and RBSM • Create SAS Data Review Listings based on protocol, EDC Database, and Data Validation Specifications • Create and maintain a library of Manual Data Review Listings • Create Safety Review Listings • Participate in creating reports and listings supporting Centralized Monitoring • Document changes to code and specifications • Assist in developing SOPs related to implementation of data standards • Assist with strategies to increase productivity and quality while decreasing cycle times and costs • Mentor junior Analysts and Programmers • Conduct activities in conformance with regulatory requirements, industry guidelines, SOPs, sponsor requirements, and timelines

🎯 Requirements

• A Bachelor of Science degree is required • At least 10 years of clinical research experience in the biotechnology, pharmacy or CRO industry, including 5 years of SAS programming • Excellent knowledge of regulatory requirements and the drug development process • Extended exposure to clinical trial data, SAS data, and database specifications • Strong verbal and written communication skills in English • Ability to work in a high-speed environment with proven agility to juggle and prioritize multiple competing demands • SAS certification and/or Advanced Programmer experience would be assets • Very organized and focused on details, with effective project planning and time management skills • Must be legally able to work in Argentina

🏖️ Benefits

• Flexible work schedule • Permanent full-time position • Ongoing learning and development • Attractive advancement opportunities • Equal opportunity and accommodations throughout the recruitment and selection process, upon request