Senior Clinical Analyst & SAS Programmer Lead

Indero

Buenos Aires

On-site

ARS 1,200,000 - 1,900,000

Full time

10 days ago

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Benefits offered by this job

Flexible work schedule

Permanent full-time position

Ongoing learning and development

Job summary

Indero is seeking a Senior Clinical Analyst and Programmer to lead programming for various data listings used in data review, Safety Review Listings, Centralized Monitoring Listings and Reports. You will translate DM and RBSM needs into code within agreed timelines and budget, while helping develop SOPs and strategies to increase productivity and quality in a fast-paced environment.

Requires 10+ years in clinical research and 5+ years SAS programming, with strong English communication and

Qualifications

A Bachelor of Science degree is required.
Master's degree in Computer Science, Information Technology Systems, Statistics, Engineering, or a related field is an asset.
At least 10 years of clinical research experience in biotech/pharma/CRO, including 5 years of SAS programming.
Regulatory requirements and drug development knowledge are essential.
Strong English verbal and written communication skills.
Organized with solid time management and project planning abilities.
Ability to work in a high-speed environment with multiple priorities.

Responsibilities

Lead programming activities for listings, reviews, and reports for data review, Safety Review Listings, Centralized Monitoring Listings and Reports.
Gather, analyze, and translate DM and RBSM needs into code within timelines and budget.
Create SAS Data Review Listings based on protocol, EDC database and Data Validation Specs.
Build a library of Manual Data Review Listings and Safety Review Listings.
Assist in developing SOPs related to data standards and promote best practices.
Document changes to code and specifications.
Mentor junior Analysts and Programmers to enhance skills and productivity.
Contribute to reports and listings supporting Centralized Monitoring.