Clinical Development Scientist, Senior Manager

Scorpion Therapeutics; New York (NY); Hybrid; USD 180,000 - 240,000; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

Scorpion Therapeutics is seeking a Senior Manager, Clinical Development Scientist to oversee internal medicine trials with a focus on scientific integrity, data quality, and regulatory compliance. The role emphasizes leadership, collaboration, and mentoring, including potential supervisory responsibilities.

The position requires advanced degrees with substantial clinical research experience in biopharma, along with strong regulatory and cross-functional coordination skills.

Qualifications

• PhD or PharmD with 1+ years in clinical development.
• MA/MS with 5+ years in clinical research within biopharma.
• BA/BS with 6+ years in clinical research.
• Biopharma industry background.

Responsibilities

• Provide clinical development oversight for internal medicine trials.
• Input protocol and support clinical operations.
• Review safety and data for trials.
• Contribute to regulatory documents and submissions.
• Support site selection and investigator interfaces.
• Assist with audits and regulatory interactions.

Skills

Clinical development

Leadership

Regulatory knowledge

Data review

Education

PhD/PharmD

MA/MS

BA/BS

Tools

GxP compliance

Job description

Role: Senior Manager, Clinical Development Scientist overseeing clinical trials in Internal Medicine. Primary objectives include ensuring scientific integrity, data quality, and compliance across studies, with potential supervisory responsibilities. Emphasizes leadership, collaboration, and mentoring capabilities.

Responsibilities

• clinical support
• protocol input
• safety and data review
• regulatory document contributions
• site selection
• investor interface
• audit preparedness

Requirements

• PhD/PharmD with 1+ year
• MA/MS with 5+ years
• BA/BS with 6+ years of clinical research experience
• biopharma industry background

Preferred

• cardiometabolic disease expertise
• experience in study design
• regulatory submissions
• scientific publication record

High-value

• involvement in clinical phases
• GxP compliance
• data review
• safety monitoring
• regulatory interactions within internal medicine

Work setup

Hybrid role based in the U.S., with global travel possible.