Senior Clinical Development Scientist – Oncology & CAR-T

Kite Pharma, Inc.; Greater London; On-site; GBP 60,000 - 90,000; Full time

Job summary

Kite Pharma, Inc. is seeking a role focused on late-stage oncology clinical development. You will collaborate on program implementation, start-up/execution/close-out, data analysis, reporting, and regulatory support for ongoing trials.

Responsibilities include contributing to study design, protocols, data listings, and regulatory documents, while adhering to GCP and SOPs. Strong regulatory knowledge and CAR-T experience are valued.

Qualifications

• Typically requires a PharmD or PhD in clinical research or clinical pharmacology with scientific and/or 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.
• Relevant experience in Multiple Myeloma and/or CAR-T Therapy is preferred.
• Experienced with Microsoft Office and other job-related programs.

Responsibilities

• Acquires and uses knowledge of clinical trial design to develop study concepts and protocols.
• Participates in protocol review discussions on study design.
• Prepares study protocols, amendments, and Investigator meeting notebooks with guidance.
• Contributes to CRFs, Data Management Manuals, and Data Analysis Plans with supervision.
• Addresses questions from Investigators regarding scientific and procedural issues.

Skills

Analytical abilities

Fast learner

Strong communication

Regulatory knowledge

Microsoft Office

Education

PharmD or PhD in clinical research or clinical pharmacology

MS with 6+ years’ relevant scientific and/or drug development experience

BS or RN with 8+ years’ relevant scientific and/or drug development experience

Tools

FDA knowledge

EMA regulations

Job description

Kite Pharma, Inc. is seeking a role focused on late-stage oncology clinical development. You will collaborate on program implementation, start-up/execution/close-out, data analysis, reporting, and regulatory support for ongoing trials.

Responsibilities include contributing to study design, protocols, data listings, and regulatory documents, while adhering to GCP and SOPs. Strong regulatory knowledge and CAR-T experience are valued.