Manager, Global Clinical Programs

Company Overview

ImmunityBio, Inc. (NASDAQ : IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.

We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system.

Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow.

The goal : to reprogram the patient's immune system and treat the host rather than just the disease.

Why ImmunityBio?

• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.

Position Summary

The Manager, Global Clinical Programs (MGCP) will serve as the clinical operations leader in an assigned therapeutic program.

This individual will be responsible for implementing the company's goals and priorities as they relate to the assigned therapeutic program.

The MGCP must be effective in leading clinical research staff as well as being accountable to the highest levels of management.

They will be an expert with regards to the clinical operations and status of the assigned therapeutic program. This is a highly visible role within the company.

Essential Functions

• Lead a team of Clinical Trial Managers, Clinical Research Associates and Clinical Trial Associates to meet the goals and timelines of the assigned therapeutic program.
• Act as the representative for program's global clinical operations to functional group leaders, external vendors, and senior management.
• Partner effectively and synergistically with stakeholders across the entire company
• Manage, train and mentor Clinical Trial Managers on day-to-day activities and strategic initiatives.
• Performs other special projects and duties as assigned.

Education & Experience

• Minimum of Bachelor's degree in science (Master's or PhD preferred)
• At least 7 years of experience working as a Clinical Trial Manager or Clinical Program Manager
• Experience with feasibility, project, budget, and resource management.
• Global experience managing Clinical Research Organizations (CROs), central labs and other vendors required
• Previous people management experience.
• Previous experience working in a dynamic and fast-paced environment.
• Comfortable working directly with the highest levels of the company.
• Experience in NDA submissions, experience with BLA submissions is ideal.
• Strong background in oncology clinical development

Knowledge, Skills, & Abilities

• Demonstrated ability working directly with the highest levels of the company with ease
• Excellent verbal and written communication skills in English
• Knowledge of FDA guidelines as well as ICH / GCP Guidelines.
• Deep understanding of the drug development process and prior experience in the biopharmaceutical industry.
• Excellent time- and project-management skills, attention to detail, and ability to balance multiple projects simultaneously
• Strong critical and logical thinking with ability to analyze problems, identify alternative solutions, and implement recommendations for resolution
• Ability to work collaboratively in a dynamic environment
• Ability to mentor and develop junior employees within the assigned therapeutic program and more broadly across the clinical operations organization
• Highly proficient in, MS Office (Word, Excel, PowerPoint, Outlook), Adobe Acrobat, eTMF, CTMS, and eCTD authoring templates
• Maintain corporate confidentiality at all times.

Working Environment / Physical Environment

• This position will work on site
• Ability to work flexible hours for various time zones (management located in Southern California)
• Ability to travel as needed on a limited basis

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below.

The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$166,000 (entry-level qualifications) to $190,000 (highly experienced)

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families.

Our competitive total rewards benefits package, for eligible employees, include : Medical, Dental and Vision Plan Options

• Health and Financial Wellness Programs
• Employer Assistance Program (EAP)
• Company Paid and Voluntary Life / AD&D, Short-Term and Long-Term Disability
• Healthcare and Dependent Care Flexible Spending Accounts
• 401(k) Retirement Plan with Company Match
• 529 Education Savings Program
• Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks
• Paid Time Off (PTO) includes : 11 Holidays
• Exempt Employees are eligible for Unlimited PTO
• Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day
• We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and / or expression, or other status protected by law.

ImmunityBio is a mandatory vaccination employer for COVID-19 and its variants. The Company requires that its employees be fully vaccinated as of their start date.

If you require a medical or religious accommodation we will engage in the interactive process with you. Proof of vaccination will be required prior to start.

If we make you an offer and you are not yet vaccinated, we will accommodate a delay in start date. ImmunityBio may also mandate that its employees receive vaccine boosters, and all accommodation laws will be followed.