Clinical Application Specialist I

job summary: Are you a skilled Clinical Application Specialist seeking a high-impact, fully remote opportunity? A Top-Tier Global Pharma Leader is hiring a Clinical Application Specialist I for a 1-year contract role. This position offers complete remote flexibility while driving cutting-edge Real-World Data (RWD) and Real-World Evidence (RWE) analyses across multiple therapeutic areas, with a key focus on AI-driven data initiatives and obesity research.

location: Telecommute job type: Contract salary: $35.00 - 45.91 per hour work hours: 9 to 5 education: Masters

responsibilities:

• Support Real-World Data (RWD) and Real-World Evidence (RWE) analysis across therapeutic areas, focusing on AI initiatives and obesity research.
• Contribute to the design and execution of pharmacoepidemiologic studies, protocol development, and statistical analysis plans.
• Evaluate, synthesize, and present epidemiology literature and secondary data sources, including administrative claims and health records.
• Generate and validate tables, listings, and graphs for clinical compound projects in compliance with quality assurance standards.
• Support key safety, risk management plans, and regulatory deliverables.

qualifications: Required:

• Master’s degree (MPH, MS, Statistics, Epidemiology, or Pharmacy) or Ph.D./MD/PharmD in a related discipline.
• Strong proficiency in SAS programming; experience with SQL, R, or Python.
• Solid background in disease epidemiology, population sizing, and handling Electronic Medical Records (EMR) or disease registries.
• Excellent cross-functional communication and literature synthesis skills.

Preferred:

• Direct pharmaceutical or biotech industry experience.
• Prior clinical research or outcomes research background.

skills: SAS, R Language

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

,

• Support Real-World Data (RWD) and Real-World Evidence (RWE) analysis across therapeutic areas, focusing on AI initiatives and obesity research.
• Contribute to the design and execution of pharmacoepidemiologic studies, protocol development, and statistical analysis plans.
• Evaluate, synthesize, and present epidemiology literature and secondary data sources, including administrative claims and health records.
• Generate and validate tables, listings, and graphs for clinical compound projects in compliance with quality assurance standards.
• Support key safety, risk management plans, and regulatory deliverables.

SAS, R Language