Katalyst CRO
Posted 31 days agoVerified live 1d ago
Business Analyst – Clinical Trials
Brief overview
Remote
32 H-1B approvalsDept. of Labor
9 green cardsCertified filings
Clinical Trials Business AnalysisLife Sciences Business AnalysiseSourceDirect Data Capture (DDC)eCOA/ePROClinical Trial WorkflowsClinical Data CaptureClinical Practice (GCP)FDA 21 CFR Part 11Business Requirements Documents (BRD)Functional SpecificationsUser Acceptance Testing (UAT)ValidationCDISC/SDTM
About the company
Katalyst CROkatalysthls.com
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide.
Visa sponsorship history
4 years sponsoring, last filed FY2026
Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.32H-1B approved
89%approval rate
3new H-1B hires
9PERM certified
$240,000median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
202319
20249
20254
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20236
20242
20259
20262
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20235
20241
20253
Top sponsored roles
VALIDATION ENGINEERQUALITY ENGINEERCLINICAL DATA ANALYSTPRODUCT DEVELOPMENT ENGINEERCLINICAL DATA MANAGER
Sponsored employees from
India
Job description
Summary
Katalyst CRO is seeking a Business Analyst to support clinical trials and life sciences projects. The role focuses on clinical trial workflows, data capture, eSource, DDC, eCOA/ePRO, business requirements, functional specifications, user acceptance testing, and validation.
Skills
- Clinical Trials / Life Sciences BA experience
- ESource, DDC, eCOA / ePRO experience
- Clinical trial workflows & data capture
- GCP, FDA 21 CFR Part 11
- BRD, Functional Specs, UAT & Validation
- CDISC / SDTM knowledge preferred
Qualifications
Must Haves
- Clinical Trials / Life Sciences BA experience
- eSource, DDC, eCOA / ePRO experience
- Clinical trial workflows & data capture
- GCP, FDA 21 CFR Part 11
- BRD, Functional Specs, UAT & Validation
Nice to Haves
- CDISC / SDTM knowledge preferred
Benefits
- Remote work arrangement
