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Clinical Research Nurse- Full Time Days

1+ years
Not Disclosed
10 Nov. 14, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Nurse – Full Time (Day Shifts)

Location: Las Vegas, Nevada, USA
Job ID: R-01331634
Job Type: Full Time
Category: Clinical Research
Work Arrangement: Fully Onsite
Shift: 12-hour day shifts


About the Organization

Thermo Fisher Scientific’s PPD® clinical research services support end-to-end clinical trial operations globally across 100+ countries. The Clinical Research team drives the development of life-changing therapies by ensuring quality, accuracy, and patient safety.


Role Overview

The Clinical Research Nurse supports the execution of multiple in-patient clinical trials, ensuring patient safety, protocol adherence, and a positive patient experience throughout the study lifecycle.


Key Responsibilities

1. Patient Screening & Enrollment

  • Review inclusion/exclusion criteria with patients.

  • Coordinate with Principal Investigator (PI) for eligibility confirmation.

  • Review and witness the informed consent process.

  • Prepare study-specific documentation for trial visits.

2. Patient Safety & Clinical Monitoring

  • Monitor and assess adverse events (AEs).

  • Report any serious findings to the Investigator/physician.

  • Ensure complete adherence to GCP, ICH, FDA, OSHA standards.

3. Clinical Procedures

Perform all relevant in-patient procedures including:

  • Patient check-ins & recovery management

  • Gauze management

  • Administration of investigational drugs (oral, IV, topical, etc.)

  • Blood draws

  • Vital signs

  • ECGs

  • Specimen processing and handling

4. Study Conduct & Compliance

  • Attend initiation meetings as needed.

  • Support multiple ongoing studies simultaneously.

  • Continuously ensure a positive patient experience.

  • Oversee staff adherence to clinical guidelines.

5. Additional Duties

  • Perform other study-related tasks as per training and certification.

  • Respond to medical emergencies per ACLS and protocol procedures.


Required Qualifications

Education

  • RN or LVN degree from an accredited institution.

  • Active nursing license (State of Nevada).

Experience

  • Minimum 1 year of experience as an RN or LVN.

  • Experience in oral surgery clinical settings preferred.

Knowledge, Skills & Abilities

  • Ability to administer investigational drugs using various routes.

  • Skilled in technical procedures: blood draw, ECG, vital signs, lab specimens.

  • Strong organizational and multitasking abilities.

  • Good handwriting and high attention to detail.

  • Excellent verbal & written communication skills.

  • Ability to work well in a team and interact professionally with staff, patients, and clients.

  • Basic computer literacy.


Work Environment & Physical Requirements

  • Office/clinic setting with exposure to electrical equipment & biohazard materials.

  • Frequently stationary for 4–6 hours.

  • Repetitive hand movements required.

  • Light to moderate lifting (15–20 lbs).

  • Occasional travel/driving may be required.

  • Must be reachable via cell phone after hours.

  • Frequent long hours, weekends, or holidays based on study needs.

  • Ability to perform under stress and adapt to changing conditions.


Benefits

  • Competitive compensation

  • Annual incentive bonus

  • Healthcare and insurance benefits

  • Strong career development opportunities

  • Innovative and inclusive company culture (Integrity, Intensity, Involvement, Innovation)