Job Overview
Location
Remote
Job Type
Full-time
Category
Product Management
Date Posted
June 23, 2026
Full Job Description
đź“‹ Description
- • Develop, review, and update clinical study training materials including site initiation slides, informed consent form templates, procedures manuals, and laboratory and pharmacy manuals.
- • Interpret the medical and scientific intent of clinical protocols, including study procedures, logistics, subject safety, and data evaluation methods.
- • Communicate the scientific rationale of assigned clinical studies to internal teams and external clinical sites.
- • Serve as the Subject Matter Expert for clinical sites, providing guidance on protocol interpretation, eligibility criteria, and regulatory compliance.
- • Create, edit, distribute, and collect site feasibility questionnaires to support study start-up activities.
- • Oversee and support the collection and review of essential regulatory and study documents during clinical trial initiation.
- • Collect and maintain study and site metrics, including tracking key performance indicators and study progress using internal trackers.
- • Participate in case report form (CRF) data review and source document verification, resolving data queries in collaboration with clinical sites.
- • Coordinate regular communication with field and in-house Clinical Research Associates before and after site visits to ensure alignment and issue resolution.
- • Partner with field CRAs to identify, troubleshoot, and resolve operational issues identified during site monitoring visits.
- • Collaborate with Supply Chain to ensure clinical sites maintain adequate investigational product (IP) inventory and address temperature monitoring excursions.
- • Train investigators, study coordinators, and vendors on study-specific requirements, procedures, and regulatory expectations.
- • Review clinical specimen logs and coordinate the shipment of specimens to the sponsor or contracted vendors.
- • Conduct remote monitoring activities, including reconciliation of investigational product accountability and documentation review.
- • Provide mentorship and onboarding support to newly hired Clinical Research Associates and other research staff.
- • Maintain strict adherence to company SOPs, ICH E6 guidelines, and Code of Federal Regulations throughout all clinical trial activities.
- • Ensure corporate confidentiality and data integrity at all times during clinical trial operations.
- • Work independently with minimal supervision while maintaining high accuracy in documentation, communication, and compliance tasks.
- • Travel up to 75% of the time as required by study protocols and site monitoring needs.
- • Operate effectively across multiple time zones with flexible working hours to support global clinical trial operations.
- • Utilize clinical trial systems including EDC, eTMF, CTMS, MS Word, Excel, PowerPoint, Outlook, and Adobe for daily responsibilities.
- • Demonstrate strong organizational, time management, and multi-tasking skills to manage multiple studies and deadlines simultaneously.
- • Exhibit an outgoing, confident demeanor and persuasive communication style to influence and guide clinical site personnel.
- • Identify operational issues proactively and propose practical, compliant solutions to internal teams and external partners.
- • Complete projects reliably with minimal oversight and maintain accountability for deliverables across all assigned studies.
🎯 Requirements
- • Bachelor’s degree in clinical research, science, or health-related field with 6 years of clinical research experience OR high school diploma with 8 years of clinical research experience
- • Minimum of 2 years’ experience as a Clinical Research Associate II or higher
- • Proficiency in EDC, eTMF, CTMS, MS Office Suite, and Adobe
- • Working knowledge of ICH E6 and Code of Federal Regulations
- • Ability to travel up to 75% of the time
- • Strong written and oral communication skills with ability to serve as Subject Matter Expert
🏖️ Benefits
- • Medical, Dental, and Vision Plan Options
- • Health and Financial Wellness Programs
- • Employer Assistance Program (EAP)
- • 401(k) Retirement Plan with Company Match
- • Unlimited PTO for Exempt Employees
- • Discretionary bonus and equity award eligibility
Skills & Technologies
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About NantWorks, LLC
NantWorks is a diversified holding company founded by Dr. Patrick Soon-Shiong that invests in and operates businesses across biotechnology, healthcare data infrastructure, digital entertainment, and secure communications. Its portfolio includes initiatives in precision medicine, genomic sequencing, AI-driven clinical decision support, low-latency networking, and immersive media technologies. The company integrates advanced data analytics, cloud computing, and machine learning to accelerate biomedical research and deliver personalized therapies. Through subsidiaries and strategic partnerships, NantWorks seeks to create an integrated ecosystem linking patients, providers, researchers, and payers to improve outcomes and reduce healthcare costs while advancing innovation across its sectors.
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