Senior Scientist, Clinical Science IMM (MedTech)

Location: Spring House, Pennsylvania, United States of America

Salary: $109,000–$174,800 per year

Company

Johnson & Johnson MedTech develops healthcare and medical technology solutions focused on preventing, treating, and curing complex diseases.

What you will do

• Support clinical strategies and the execution of clinical trial protocols in accordance with scientific, organizational, and regulatory standards.
• Assist with study initiation, medical data monitoring, training, and study closeout activities.
• Review aggregate and participant-level data, analyze clinical laboratory results, and draft patient narratives for adverse events.
• Prepare and support clinical study reports, regulatory documents, and other study materials.
• Collaborate with Study Responsible Scientists, Study Responsible Physicians, Clinical Leads, cross-functional teams, CROs, and other external partners.
• Identify study-level issues requiring escalation and support product development goals within a matrixed organization.

Requirements

• Bachelor’s degree in a scientific or related discipline; an MS, PharmD, or PhD is preferred.
• At least one year of relevant clinical research and development experience in pharmaceutical, biotech, CRO, or equivalent settings.
• Understanding of regulatory guidelines and Good Clinical Practice (ICH-GCP).
• Ability to interpret scientific literature, analyze clinical data, solve problems, prioritize work, and meet deadlines.
• Excellent written and verbal English communication skills, including the ability to present information to stakeholders.
• Willingness to travel domestically and internationally approximately 10% as required by project needs.

Nice to have

• Experience with clinical data management, clinical evaluations, drug discovery and development, or regulatory affairs.
• Familiarity with Microsoft Office, clinical trial management software, and generative artificial intelligence.
• Experience with coaching, relationship building, and medical device development and regulation.

Culture & Benefits

• Inclusive workplace focused on ethical standards, participant safety, and collaboration across global matrix teams.
• Participation in pension, savings, and 401(k) plans, subject to plan terms.
• Vacation, sick time, holiday pay, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time-off.
• Eligibility for the company’s long-term incentive program.