Senior Oncology Clinical Development Scientist (CAR-T)

Kite Pharma, Inc.; Parsippany-Troy Hills (NJ); On-site; USD 150,000 - 200,000; Full time

Benefits offered by this job

Discretionary annual bonus

Stock-based long-term incentives

Paid time off

Benefits package

Medical insurance

Dental insurance

Vision insurance

Life insurance

Job summary

Kite Pharma, Inc. seeks a Clinical Scientist to support late-stage oncology clinical development. Working with the Clinical Scientist Program Lead, you will assist in program implementation, start-up/execution/close-out tasks, data analysis, reporting and regulatory filings.

Required qualifications include a PharmD or PhD or MS with relevant experience, with preference for multiple myeloma/CAR-T familiarity; strong analytical and communication skills; and willingness to travel as needed.

Qualifications

• PharmD or PhD in clinical research or clinical pharmacology with drug development experience.
• MS with 6+ years’ relevant scientific and/or drug development experience.
• BS or RN with 8+ years’ relevant scientific and/or drug development experience.

Responsibilities

• Acquires and uses knowledge of clinical trial design to develop study concept sheets and protocols.
• Participates in protocol review discussions concerning study design.
• Prepares study protocols, amendments, and manual sections with guidance.
• Contributes to design of CRFs and Data Management Manuals.
• Assists in preparation/review of regulatory documents.

Skills

Fast learner

Flexible/adaptable

Analytical abilities

Strong communication

Education

PharmD or PhD in clinical research or clinical pharmacology

MS with 6+ years’ relevant experience

BS or RN with 8+ years’ relevant experience

Tools

Microsoft Office

Job description

Kite Pharma, Inc. seeks a Clinical Scientist to support late-stage oncology clinical development. Working with the Clinical Scientist Program Lead, you will assist in program implementation, start-up/execution/close-out tasks, data analysis, reporting and regulatory filings.

Required qualifications include a PharmD or PhD or MS with relevant experience, with preference for multiple myeloma/CAR-T familiarity; strong analytical and communication skills; and willingness to travel as needed.