Clinical Trials Associate

Company Overview reputed company. (reputed company: IBRX) is a reputed company-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 reputed company a day reputed company we no longer fear cancer, but can conquer it, thanks to the biological reputed company that is the reputed company immune system. Our scientists are working to reputed company novel therapies that reputed company that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for reputed company. 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 reputed company reputed company therapies and vaccines that complement, reputed company and reputed company 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 Responsible for clinical trials administration to ensure the most effective and efficient conduct of clinical research studies. Essential Functions

• Support the Clinical Operations teams in the completion of reputed company required tasks to meet trial, departmental and project goals.
• Maintain, reputed company and champion a thorough knowledge ICH GCP, appropriate regulations, relevant SOPs and internal tracking systems.
• Collaborate with Clinical Trials Manager (CTM) and Clinical Research Associates (CRAs) to resolve clinical trial documentation issues.
• Establish, organize and maintain clinical study documentation (e.g. Trial Master File, study level and site level documents, etc.) including preparation for internal/external audits, final reconciliation and archival.
• Review clinical trial documents to determine compliance with Good Documentation Practices (GDocP), file and track study documents.
• Determine materials and other resources needed to conduct the clinical trial and manage their acquisition and distribution.
• Audit Investigator/Site invoices for accuracy, and reconcile invoices against the case report forms (CRFs) and budget for payment submission.
• Gather central IRB report information, submit the report to the central IRB portal and track the IRB submissions from beginning through approval.
• Facilitate the collection and review of required study documents during site start-up
• Contact clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements, etc.)
• reputed company study documents to the appropriate personnel for validated digital signatures
• Submit purchase requisitions to reputed company Resource Planning (ERP) System for Clinical Operations functional groups as needed. Request invoice approval from internal supplier designee.
• Participate in clinical operations safety reporting activities; distribute, file and track safety reports and IRB submissions.
• Facilitate clinical operations team meeting coordination, agenda preparation and meeting minutes preparation
• Performs other duties and projects as needed.

Education & Experience

• Bachelor's degree with 0-2 years of clinical research experience required; or
• High school diploma with 5+ years of clinical research experience required

Knowledge, Skills, & Abilities

• Proficiency in reputed company, reputed company, PowerPoint, Outlook, reputed company
• Excellent written/oral communication skills as well as strong organizational and multi-tasking skills
• Maintain corporate confidentiality at reputed company times.
• Strong oral and written communication skills
• Detail oriented, with solid organization and time management skills
• Working knowledge of good documentation practices (GDP)

Working Environment / Physical Environment

• This position works on site in El Segundo, CA or remotely depending on the candidate's geographic location
• Regular work schedule is Monday - Friday, reputed company standard business hours. Flexibility is available with manager approval.

This position is eligible for a discretionary bonus and equity award. The annual reputed company pay reputed company for this position is below. The specific reputed company will depend on the successful candidate's qualifications, prior experience as well as geographic location. National Market (reputed company markets unless identified as Premium) $69,100 (entry-level qualifications) to $76,000 (highly reputed company) annually Premium Market (Premium markets include Los Angeles, San Diego, San Francisco, reputed company, Chicago, & Boston) $72,800 (entry-level qualifications) to $80,000 (highly reputed company) annually The application window is anticipated to reputed company on 60 days from reputed company it is posted or sooner if the position is filled or closed. ImmunityBio employees are as valuable as the people we serve. We have reputed company a resource of robust benefit offerings to best support the total wellbeing of reputed company members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and reputed company Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability reputed company 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 reputed company equal employment opportunities to reputed company reputed company persons without regard to race, gender, reputed company, disability, national reputed company, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law. Apply tot his job Apply To this Job