Sr Clinical Development Scientist

Kite Pharma • Foster City, CA

1d • $153,935 - $219,120

About The Position

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. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description As part of the Clinical Development Department, the Sr Clinical Development Scientist fills a key role (Clinical Scientist) on the clinical study team within one of Kite's cellular therapy programs. Working in close collaboration with the study medical monitor, the incumbent will provide scientific guidance and support to the team. He or she will be responsible for various aspects of clinical study execution including protocol writing, building study infrastructure, staff training, data cleaning/analysis, investigator interaction and support of regulatory filings.

Requirements

• BS/BA in biomedical field and 8 + years relevant scientific and/or drug development experience -OR-
• MS in biomedical field and 6+ years relevant scientific and/or drug development experience -OR-
• PhD or PharmD and 2+ years relevant scientific and/or drug development experience
• Strong understanding of ICH GCP, as well as general knowledge of industry practices and standards.
• Excellent interpersonal, organizational, written, and verbal communication skills.
• Ability to work effectively on teams with a combination of remote and office-based team members.
• Exemplify our core values of integrity, accountability, teamwork, excellence, and inclusion.

Nice To Haves

• Advanced degree (PharmD, PhD, MS, etc.). Ideally the candidate will have experience directly in the clinical science role, in a hematology/oncology indication, and on global phase 2 and 3 studies.
• Able to translate technical concepts into accessible language and direction for the broader study team.
• Flexible and adaptable to quickly changing priorities, and willingness to move between projects to provide support/expertise as business needs dictate.
• Experienced in Microsoft Office (Excel, Word, PowerPoint, OneNote), and ideally also with job related programs such as J-Review and Medidata Rave or similar.

Responsibilities

• Integrates scientific knowledge and operational expertise to ensure translation of clinical research plans into efficiently delivered high quality studies.
• Acquires and utilizes knowledge of clinical trial design and relevant disease indications to assist with protocol development.
• Participates in discussions concerning scientific and procedural aspects of study design.
• Coordinates with other departments to produce the final protocol and informed consent documents.
• Contributes to the development of CRFs, edit checks, IVRS specifications, ongoing data cleaning (query generation, coding review, SAE reconciliation) and data trend analysis.
• Designs patient profiles and writes accompanying medical data review rules as directed by the medical monitor.
• Leads data cleaning effort in preparation for dose escalation or DSMB meetings, as applicable to study stage.
• Organizes and manages external medical advisory committees for the study team such Scientific Steering Committees, as directed by the medical monitor.
• Researches and summarizes scientific or technical information available in published literature for continual self-learning and to assist in preparing training, study manual, or investigator meeting materials.
• Participates in the review of statistical analysis plans, table, listing, figure design and presentations of study data.
• Addresses site questions regarding protocol and related scientific issues and attends site initiation visits (SIVs).
• Assists in reviewing briefing books, health authority requests for information, IND annual reports, Investigator Brochures, and other regulatory documents.
• Supports priorities within the functional area and contributes to department initiatives as requested.

Benefits

• This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
• Benefits include company-sponsored medical, dental, vision, and life insurance plans.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level