Clinical Research Nurse - Red Deer, AB TP K

Job Summary

We are seeking a full-time Clinical Research Nurse (LPN) to join our team in Red Deer.
Clinical research nurse required for clinical trials providing clinical expertise and patient care ensuring health safety of participants.
Key responsibilities include overall care educational support to patients participants review referrals medical histories determining eligibility suitability for clinical trial protocols based on assessment information. Follow GCP ICH guidelines Clinic SOPs at all times complete participant screening utilizing appropriate tools clinic procedures employing advanced knowledge skill history physical assessment assess clinical needs patients prior presenting research options determine plan based assessment adjust work schedules integrate newly approved clinical trials ongoing research activities demonstrate professional behavior dealing patients families visitors physicians healthcare providers clinic staff coordinate aspects clinical trial coordination including screening informed consent process randomization treatment follow-up study subjects arranging external services diagnostic imaging eye exams biopsies etc responsible lab sample collection processing administer study drugs supplies questionnaires implement clinical study protocols monitor daily study activities progress prepare reports updates investigators management as appropriate monitor enrolment goals modify recruitment strategies necessary ensure all clinical activities carried out established research protocols standards compliance applicable laws regulations policies including but not limited to GCP ICH Clinic SOPs maintain study regulatory documents report abnormal results adverse events serious adverse events Investigator Sponsor according study protocol local ethics board regulatory agencies sponsor requirements perform miscellaneous job-related duties assigned schedule study participant visits per protocol perform delegated protocol-specific activities vitals ECGs laboratory assessments questionnaires IP administration obtain necessary documentation required by protocol create source documents other research documents successful conduct clinical research study meet Sponsor representatives discuss conduct review data follow-up required based meeting/review raise community awareness trials CaRe Clinics contributions medical advancement.

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Job description