Senior Contracts Administrator, Research & Development

Job description

Company Overview ImmunityBio is a vertically integrated commercial stage biotechnology company developing next-generation therapies that bolster the natural immune system to defeat cancers and infectious diseases. The Company’s range of immunotherapy and cell therapy platforms, alone and together, act to drive and sustain an immune response with the goal of creating durable and safe protection against disease. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response. The Company is applying its science and platforms to treating cancers, including the development of potential cancer vaccines, as well as developing immunotherapies and cell therapies that we believe sharply reduce or eliminate the need for standard high-dose chemotherapy. These platforms and their associated product candidates are designed to be more effective, accessible, and easily administered than current standards of care in oncology and infectious diseases. 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 Senior Contracts Administrator position will provide all forms of contract-related support through all phases of the contract lifecycle. The role will partner with a variety of key business stakeholders throughout the company. Essential Functions Manage the end-to-end administrative lifecycle of clinical research agreements, including CTAs, CRO agreements/SOWs, HCP/consulting agreements, MTAs, clinical supply agreements, investigator-initiated research agreements, and related amendments. Monitor, triage, and process group email inbox used for contract requests and questions, including assignment of requests for review; assign and track action items and file processed emails. Track contracts from intake, drafting, negotiation, approval and execution; maintain comprehensive contract trackers and dashboards showing agreement status, aging, cycle times, outstanding actions, upcoming expirations, amendments, site activation dependencies, and other key metrics. Prepare first drafts of clinical research agreements by selecting and populating approved company templates with study-, site-, vendor-, investigator-, and transaction-specific information; prepare amendments, SOWs, work orders, change orders, exhibits, schedules, and other contracting documents using approved templates and established forms. Maintain and administer the company's library of approved clinical contracting templates, forms, SOWs, checklists, clause libraries, and country-specific documents under Legal supervision. Ensure only current, Legal-approved templates are used and maintain appropriate version control over contracting documents. Route contracts through the company’s required approvals process and facilitate electronic execution and finalization. Manage the signature process for clinical research agreements, including routing documents through electronic signature systems, monitoring outstanding signatures, and ensuring fully executed copies are distributed and retained. Ensure agreements are appropriately executed, stored, indexed, and associated with the relevant study, site, investigator, CRO, or vendor in the contract management system; upload contracts and input relevant data into Company’s contract management repository. Produce regular clinical contracting reports and metrics for Legal and Clinical Operations leadership. Support audits, inspections, diligence exercises, and internal reviews by locating agreements and assembling complete contracting documentation, approval records, and audit trails. Assist Legal with development and implementation of clinical research policies, SOPs, contracting procedures, checklists, templates, forms, and training materials; develop and maintain standard operating instructions and process maps for clinical contracting workflows. Identify administrative bottlenecks and recurring process issues and recommend improvements to workflows, templates, intake processes, tracking systems, and contracting technology. Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities. Education & Experience High School Diploma, with a minimum of 7+ (including but not limited to internships and/or coursework) years of relevant experience required; or Associate’s degree, with a minimum of 5+ (including but not limited to internships and/or coursework) years of relevant experience required. Knowledge, Skills, & Abilities Excellent written and oral communication skills Strong organizational skills and attention to detail Ability to exercise professionalism, poise and tact in all verbal and written correspondence Strong time management skills Ability to multitask in a fast-paced work environment Ability to set priorities under pressure Proficient knowledge of MS Office Willingness to take initiative to complete projects Good judgment and practicality Working Environment / Physical Environment This role will be an onsite role in El Segundo, CA 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. Lift and carry materials weighing up to 20 pounds. This position is eligible for a discretionary bonus and equity award. The hourly 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. $42.50 (entry-level qualifications) to $46.75 (highly experienced) per hour ImmunityBio uses artificial intelligence (AI) tools to assist with sourcing and identifying potential candidates for open positions. These tools help us reach qualified applicants and improve the efficiency of our recruitment outreach. No preference is given to applicants sourced or identified by AI tools. Important: AI is not used to screen, evaluate, rank, assess, or make hiring decisions about applicants. All applications are reviewed by human recruiters and hiring managers. Hiring decisions are made solely by ImmunityBio personnel without automated decision-making. We are committed to equal employment opportunity and ensure that all candidates are assessed based on their qualifications, skills, and experience through human review. 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.