Senior Oncology Clinical Development Scientist

Kite Pharma, Inc.; San Francisco (CA); In loco; USD 154.000 - 199.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical, dental, vision, life ins.

Discretionary annual bonus

Stock-based long-term incentives

Paid time off

Benefits package

Descrizione del lavoro

Kite Pharma, Inc. in San Francisco, CA seeks a clinical development professional to support late-stage oncology programs, collaborating on study start-up, execution, data analysis, and regulatory filings.

Responsibilities include protocol development support, CRF design, data listings and regulatory document prep. Strong FDA/EMA, ICH/GCP knowledge and excellent communication are essential for success.

Competenze

• 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.
• Experience in Multiple Myeloma and/or CAR-T therapy preferred.
• Proficiency with common office software.

Mansioni

• Support late-stage oncology clinical development and program activities.
• Collaborate on protocol reviews, study start-up/execution/close-out, and data analysis.
• Assist in regulatory filings and preparation/review of documents.
• Contribute to CRF design, Data Management Manuals, and Data Analysis Plans.
• Address questions from Investigators with supervision and prepare study materials.
• Coordinate with teams and provide direction as needed.

Conoscenze

Fast learner

Flexible

Analytical abilities

Drug development knowledge

FDA/EMA regulations

GCP knowledge

Strong communication

Organizational skills

Willing to travel

Formazione

PharmD or PhD in clinical research

MS in clinical field with 6+ years

BS or RN with 8+ years

Strumenti

Microsoft Office

Descrizione del lavoro

Kite Pharma, Inc. in San Francisco, CA seeks a clinical development professional to support late-stage oncology programs, collaborating on study start-up, execution, data analysis, and regulatory filings.

Responsibilities include protocol development support, CRF design, data listings and regulatory document prep. Strong FDA/EMA, ICH/GCP knowledge and excellent communication are essential for success.