Senior Clinical Project Scientist – IIS & CSS Lead

Biopharma Careers; Horsham (PA); On-site; USD 122,000 - 213,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

Legal insurance

Retirement plan

401(k) savings

Job summary

Johnson & Johnson in Horsham, PA is seeking an Associate Director, Clinical Project Scientist to manage Investigator Initiated Studies, collaborative groups, and company-sponsored trials in a US-focused delivery model.

The role requires cross-functional collaboration with Global Medical Affairs, GD, and TA leads to ensure timely, compliant execution and data generation across assets. Strong program management and budget skills are essential.

Qualifications

• Bachelor's degree required; advanced degree preferred.
• Oncology therapeutic area knowledge highly preferred.
• 7+ years of experience in pharmaceutical industry with IIS/collaborative trials or CSS experience.

Responsibilities

• Oversee internal review and approval of IIS, collaborative studies, and CSS.
• Collaborate with Investigators, Medical Directors, Global Medical Affairs, and other stakeholders to ensure timely execution.
• Contribute to protocol planning, informed consent, and data generation priorities across assets.
• Manage meetings to monitor study status and support IIS/collaborative proposal intake and tracking.
• Assist with contract/budget negotiations and risk mitigation strategies.
• Coordinate adverse event data collection and regulatory document incorporation.
• Lead franchise clinical initiatives and cross-functional teams when needed.
• Ensure compliance with J&J SOPs and health authority regulations.

Skills

Bachelor's degree

Oncology knowledge

7+ years experience

Presentation skills

Analytical skills

Cross-functional leadership

Education

Bachelor's Degree

Job description

Johnson & Johnson in Horsham, PA is seeking an Associate Director, Clinical Project Scientist to manage Investigator Initiated Studies, collaborative groups, and company-sponsored trials in a US-focused delivery model.

The role requires cross-functional collaboration with Global Medical Affairs, GD, and TA leads to ensure timely, compliant execution and data generation across assets. Strong program management and budget skills are essential.