Location
London

Hours
Full Time

Salary
Negotiable

About the Role
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. You will play a supportive role in late stage oncology clinical development. Working in collaboration with the Clinical Scientist Program Lead, you are accountable for various aspects of ongoing clinical trial program-related activities. These include collaboration on functional area activities during program implementation, clinical study start-up, execution, close out, data analysis and reporting, and support of regulatory filings. You will acquire and use knowledge of clinical trial design to develop study concept sheets and protocols, participate in protocol review discussions, prepare study protocols and related documents with guidance, and contribute to the design of CRFs, Data Management Manuals, and Data Analysis Plans. You will assist in addressing scientific and procedural questions from Investigators, prepare and review data listings, summary tables, study results, manuscripts, and scientific presentations, and support regulatory document preparation and review. You will anticipate and help resolve moderately complex obstacles within clinical studies and may coordinate teams or provide clinical monitoring for studies or study components. Adherence to regulatory requirements, Good Clinical Practice, and company SOPs is essential. Join Kite and help create more tomorrows.

Experience
- Typically requires a PharmD or PhD in clinical research or clinical pharmacology with scientific and/or drug development experience in biopharma, healthcare, consulting, academia, or related environments.
- 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.

About you
- Demonstrated ability to be a fast learner.
- Flexible and adaptable to change, able to move between projects and provide support where needed.
- Proven analytical abilities demonstrated through past experience and/or academic research.
- Understands drug development phases and clinical trial nature across phases.
- Knowledge of FDA and EMA regulations, ICH guidelines, GCP, and familiarity with standard clinical procedures.
- Strong communication and organizational skills.

Qualifications
- PharmD, PhD, MS, BS, or RN degrees as outlined above.
- Scientific and drug development experience relevant to clinical research.
- Commitment to regulatory compliance and Good Clinical Practice standards.