Per Diem Research Nurse — Mobile Clinical Trials

Syneos Health, Inc.; Washington; On-site; USD 69,000 - 83,000; Full time

Benefits offered by this job

Company car or car allowance

Medical, Dental and Vision benefits

401k company match

Employee Stock Purchase Plan

Bonuses based on performance

PTO and sick time

Job summary

Illingworth Research Group in Vancouver, WA is seeking a Per Diem Research Nurse to support clinical trials across phases. You will work with the RN team to visit sites, collect data, administer study medications, and ensure protocol adherence.

The role requires an RN with at least 2 years post-qualification experience, GCP certification, and strong communication skills. You will handle documentation, data entry, adverse event reporting, and coordination with stakeholders.

Qualifications

• Registered nurse with a minimum of 2 years' post qualification experience.
• GCP certification.
• Knowledge of research design and methodology desirable.
• Experience with Venepuncture and ECG preferable.

Responsibilities

• Fully conversant with trial protocol, CRFs/eCRF, off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs.
• Coordinate (working with the RN team) and complete subject trial visits on- and off-site.
• Maintain accurate documentation including electronic transfer of data as per SOPs throughout the trial, ensuring subject confidentiality and data protection.

Skills

Nursing

Communication skills

Time management

Education

RN qualification

Tools

Outlook

Word

Excel

PowerPoint

Job description

Illingworth Research Group in Vancouver, WA is seeking a Per Diem Research Nurse to support clinical trials across phases. You will work with the RN team to visit sites, collect data, administer study medications, and ensure protocol adherence.

The role requires an RN with at least 2 years post-qualification experience, GCP certification, and strong communication skills. You will handle documentation, data entry, adverse event reporting, and coordination with stakeholders.