Senior Scientist, Clinical Science IMM

Scorpion Therapeutics; Spring House (PA); On-site; USD 120,000 - 170,000; Full time

Job summary

Johnson & Johnson's Therapeutic Area in Spring House, PA is seeking a Senior Clinical Scientist to support clinical research across early to late-phase development. You will assist with protocol development, data review, and regulatory document preparation, collaborating with physicians, scientists, and cross-functional teams.

Responsibilities include supporting trial initiation, monitoring, and closeout, and contributing to scientific and compliance standards in multi-regional trials.

Qualifications

• Bachelor's degree in a scientific discipline is required.
• Advanced degrees (MS, PharmD, PhD) are preferred.
• Minimum 1 year in clinical research within pharma, biotech, or CRO.

Responsibilities

• Assist with clinical trial protocol development and data review.
• Prepare regulatory documents and ensure regulatory compliance.
• Collaborate with physicians, scientists, and cross-functional teams.

Skills

GCP

Regulatory guidelines

Data review

MS Office

Clinical trial management tools

AI

Data management

Regulatory affairs

Scientific research

Biologics/Small molecules development

Education

Bachelor's degree in a scientific discipline

MS/PhD/PharmD preferred

Tools

MS Office

Clinical trial management tools

Job description

Role

Senior Clinical Scientist supporting clinical research within Johnson & Johnson's Therapeutic area, focusing on early to late-phase development activities. Responsibilities include assisting with clinical trial protocol development, data review, and regulatory document preparation; collaborating with physicians, scientists, and cross-functional teams; supporting trial initiation, monitoring, and closeout; and contributing to scientific and compliance standards.

Qualifications

Bachelor's degree in a scientific discipline required; advanced degrees (MS, PharmD, PhD) preferred; minimum 1 year in clinical research within pharma, biotech, or CRO.

Skills

understanding of GCP, regulatory guidelines, data review, literature interpretation, and proficiency with MS Office; familiarity with clinical trial management tools and AI is advantageous. Preferred skills include data management, regulatory affairs, and scientific research. Experience with biologics or small molecules in clinical development stages (preclinical to Phase 3) and experience in multi-regional trials are desirable. Cross-functional collaboration, strong communication, organizational, and problem-solving skills are essential.

Travel

Travel approximately 10% domestically and internationally.

Work setup

Based in Spring House, PA, with potential for domestic and international travel.