Clinical Research Jobs in USA – Clinical Research Specialist Job Openings – Apply Now
Clinical research jobs continue to grow rapidly across the healthcare and MedTech sectors, and the Clinical Research Specialist role at Johnson & Johnson is one of the most sought-after opportunities in the United States. This role offers professionals a chance to contribute directly to clinical trials, R&D operations, and the development of breakthrough medical technologies. Whether youโre exploring Johnson & Johnson careers or searching for top-tier jobs in the United States of America, this position blends innovation, purpose, and career advancement.
About Johnson & Johnson
Johnson & Johnson is a worldwide leader in healthcare innovation, combining biology, technology, and medical science to build solutions that improve lives. With a strong commitment to R&D, MedTech advancements, and employee well-being, the company offers unmatched opportunities for professionals exploring Johnson & Johnson careers or searching for high-impact clinical research jobs in the United States of America.
Job Details:ย
- Job Title: Clinical Research Specialist
- Location: Irvine, California, United States of America
- Function: R&D Operations
- Sub Function: Clinical Trial Project Management
- Category: Analyst, Clinical Trial Project Management (P4 โ E24)
- Work Pattern: Hybrid Work
- Requisition Number: R-044033
- Posting Closure: November 24, 2025
- Anticipated Base Pay Range: $90,100.00 โ $121,900.00
Position Summary
The company is seeking a Clinical Research Specialist to support one or more clinical trials within the Clinical R&D Department. This role involves collaboration across multiple teams and ensuring smooth execution of clinical trial activities.
Key Responsibilities
Under general direction and in compliance with all applicable regulations and company procedures, you will:
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Serve as a Clinical Research Specialist supporting company-sponsored clinical trials under supervision.
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Participate in feasibility, site selection, study setup, conduct, and closure phases in alignment with ICH-GCP, regulatory standards, and SOPs.
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Act as primary contact for clinical trial sites, if applicable.
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Assist in developing clinical trial documents, including protocols, informed consent forms, CRFs, monitoring plans, study manuals, investigator brochures, and annual reports.
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Ensure proper registration and updates on clinicaltrials.gov.
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Coordinate ordering, tracking, and management of investigational products and study materials.
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Collaborate with investigators, site staff, IRBs/ECs, vendors, and company teams.
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Support the development and execution of investigator agreements and trial payments.
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Assist with clinical data review and preparation for statistical analysis and publications.
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Perform monitoring visits (qualification, initiation, interim, close-out), if applicable.
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Support on-site protocol compliance and data collection activities, if required.
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Track assigned project budgets and maintain accurate project knowledge for stakeholders.
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Ensure compliance with all federal, state, local, and corporate regulations and policies.
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Perform additional duties as assigned.
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Make independent decisions in simple scenarios; seek guidance for more complex issues.
Qualifications / Requirements
Education
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Bachelorโs degree in Science or equivalent field required.
Experience & Skills
Required:
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2+ years of relevant experience in a clinical researchโrelated field.
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Strong understanding of clinical trial workflow.
Preferred:
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Experience with eTMF systems.
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Experience with CTMS.
Other Requirements
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Up to 20% travel required.
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All applications will be reviewed despite a pre-identified candidate.
Required Skills for Clinical Research Jobs in USA
- Analytical Reasoning
- Clinical Data Management
- Clinical Trial Design
- Medical Knowledge
- Research & Development
- Project Management
- Clinical Research Regulations
- Trial Execution
- Ethics & Compliance
- Laboratory Operations
- Training Administration
- Process Orientation
