Data Manager, ACDS Informatics

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 90,000 - 140,000; Full time

Benefits offered by this job

Hybrid work environment

Travel up to 10%

Job summary

Scorpion Therapeutics seeks a Data Manager specializing in pharmaceutical analytical data and regulatory submissions to support decision‑making across drug development stages. You will design automated data workflows, build dashboards using Spotfire and Power BI, and collaborate with scientists, regulatory, and digital teams to translate needs into scalable digital solutions.

Requires GxP experience, data integrity, laboratory informatics, and proficiency with SQL/SAS; hybrid work with travel is

Qualifications

• Bachelor's degree in a relevant field and 10+ years in pharmaceutical data management, informatics, analytics, or regulatory support.
• Experience with data governance, data integrity, and GxP.
• Proficiency in data visualization and laboratory informatics.

Responsibilities

• Deliver compliant, submission-ready data for regulatory filings.
• Design automated data workflows and scalable digital solutions.
• Develop dashboards using Spotfire and Power BI and collaborate across functions.

Skills

Spotfire

Power BI

SQL

SAS

Data visualization

GxP

Data integrity

Education

Bachelor's degree in Chemistry / Pharmaceutical Sciences / Biology / Data Science

Tools

Spotfire

Power BI

SQL

SAS

Job description

Role: Data Manager specializing in pharmaceutical analytical data and reporting to support regulatory submissions and scientific decision-making across drug development stages.

Responsibilities

deliver compliant, submission-ready data; design automated workflows; develop dashboards using tools like Spotfire and Power BI; collaborate with scientists, regulatory, and digital teams to translate needs into scalable digital solutions; promote data standards, integrity, and process modernization; support laboratory informatics platform enhancements and governance.

Qualifications

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biology, Data Science, or related field; 10+ years (or master's with 6+ years, Ph.D. with 3+ years) in pharmaceutical data management, informatics, analytics, or regulatory support; experience with GxP, data integrity, laboratory informatics, and visualization tools (e.g., SQL, SAS).

Preferred

knowledge of CMC regulatory submissions, cloud analytics, generative AI, and digital transformation leadership.

High-value specifics

supporting analytical data for regulatory filings, working across QA, R&D, and regulatory functions; focus on laboratory informatics, automation, and data democratization; 10% travel; hybrid work environment.