Clinical Development Scientist, Senior Manager

Scorpion Therapeutics; Pennsylvania; Hybrid; USD 140,000 - 200,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Manager, Clinical Development Scientist to oversee internal medicine trials, focusing on protocol development, data integrity, safety oversight, and regulatory interactions. You will lead study design, conduct risk assessments, and ensure compliance across GxP and industry standards.

The role may involve mentoring junior staff, coordinating cross-functional teams, and managing global travel for site visits and audits, while operating in a hybrid work

Qualifications

• PhD, PharmD, or equivalent with 1+ years in clinical research.
• MA/MS with 5+ years in clinical research.
• BA/BS with 6+ years in clinical research.

Responsibilities

• Oversee clinical trials in Internal Medicine with focus on protocol development, data integrity, safety, and compliance.
• Support study design, safety monitoring, regulatory submissions, and data review.
• Coordinate stakeholder communications and provide supervision/mentorship as needed.

Skills

Clinical research

Regulatory knowledge

Study design

Education

PhD/PharmD or equivalent

MA/MS with 5+ years

BA/BS with 6+ years

Job description

Role: Senior Manager, Clinical Development Scientist overseeing clinical trials in Internal Medicine, focusing on protocol development, data integrity, safety, and compliance.

Responsibilities include supporting study design, safety monitoring, regulatory submissions, data review, and stakeholder communications, with potential supervision and mentorship duties.

Qualifications: PhD, PharmD, or equivalent with 1+ years; or MA/MS with 5+ years; or BA/BS with 6+ years of industry experience in clinical research.

Preferred: cardiometabolic disease expertise, experience in study start-up to close-out, regulatory and GxP knowledge, scientific publication record, leadership skills, and ability to manage complex projects and teams.

High-Value: involvement in biopharma clinical development, study design, safety oversight, and regulatory interactions within internal medicine or cardiometabolic areas.

Work Setup: hybrid (onsite ~2.5 days/week) with global travel required.