Specialist II, Regulatory Lifecycle Maintenance

Company OverviewImmunityBio, 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 SummaryThe Specialist II, Regulatory Lifecycle Maintenance will contribute to the development and maintenance of global clinical for investigational and marketed products and contribute towards the preparation of dossiers in eCTD format. This position will support the organization in the management and conduct of clinical programs, clinical programs and preparation of documentation to support clinical submissions including the preparation of clinical reports and summaries,Essential FunctionsReview clinical data, reports, and summaries for compliance with the protocol, statistical analysis plan, monitoring guidelines, and data management plan.Contribute to the design, central monitoring, and reporting of clinical studies performed by IBRX or by CROs.Assist with written summaries for regulatory submissions including INDs, NDAs, and BLAsContribute to the preparation or review of documents including Investigator’s Brochures, protocols, Clinical Study Reports, annual reports, DSURs, clinicaltrials.gov entries, etc.,Ensure that all documents are properly labeled, dated, and stored in accordance with company policies and regulatory requirementsEnsure compliance with BLA, MAA, IND, and CTA, submission and reporting requirements with the U.S. and ex-U.S. Health AuthoritiesReview submission packages including version verification, link checking, and coordination with the publishing group.Maintain accurate records of filed documents, including updating tracking systems and databases as neededCreate and maintain project plansParticipate in cross-functional teams and provide support to others in the preparation, analysis, and documentation of studiesServe as a trainer for RA SOPs, processes, and templates for review, preparation, QC, and finalization of documents and major sections of applications.Perform ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.Education & ExperienceBachelor’s degree in life sciences or a related field required; 3+ years of relevant regulatory clinical Science experience is required; ORMaster’s degree in life sciences or a related field required; 2+ years of relevant regulatory clinical Science experience is required2+ years clinical programs experience in the biotechnology or pharmaceutical industry preferredExperience in the preparation of the submission of clinical modules in eCTD format is preferredFamiliarity with organizing responses to Health Authority information requests is preferredFamiliarity with regulatory submissions internationally is preferred.Knowledge, Skills, & AbilitiesKnowledge of Health Authority clinical guidance documents and requirementsKnowledge of clinical research, Good Clinical Practices, and regulatory requirements and guidelinesStrong Attention to detailStrong knowledge of clinical documentation and terminologyAbility to work with firm deadlines and adapt quickly to changing requirements and prioritiesStrong organizational skills, written and oral communication skills, and attention to detailWorking Environment / Physical EnvironmentThis position works on-site in Summit, NJ.Regular work schedule is Monday – Friday, within standard business hours. Flexibility is available with manager approval.Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.This desk-based role involves close study of scientific and regulatory documents.This position will work closely with scientific colleagues throughout the day, often on a project-team basis.Lift and carry materials weighing up to 20 pounds.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.$110,000 (entry-level qualifications) to $121,000 (highly experienced) annuallyThe 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.