Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Registered Nurse Clinical Trial Regina, Saskatchewan, Canada

Propharma
Propharma
2+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Registered Nurse Clinical Trial - Regina, Saskatchewan, Canada

Location: Regina, Saskatchewan, Canada
Job Category: Clinical Trial Nursing
Time Type: Part-time
Posted on: 4 Days Ago

Apply Now

About ProPharma:

ProPharma has been advancing patient health for over 20 years by providing expert advice and solutions to biotech, pharmaceutical, and medical device companies. Through a comprehensive advise-build-operate model, ProPharma offers customizable consulting solutions that de-risk and accelerate drug and device programs. With expertise in regulatory sciences, clinical research, pharmacovigilance, and more, ProPharma supports clients throughout the product lifecycle.

Position Overview:

ProPharma is seeking a Registered Nurse Clinical Trial to join our team in Regina, Saskatchewan, Canada. This part-time role involves providing Direct Clinical Visit (DCV) services outside the investigator site, collaborating with the clinical research team, and ensuring the safety and well-being of study patients.

Key Responsibilities:

  • Complete study-specific requirements, including GCP and IATA (dangerous goods) training.

  • Provide quality DCV services at locations outside of the investigator site (e.g., home, office, school).

  • Collaborate with the Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to complex problems.

  • Document source information during DCVs in adherence to Good Documentation Practices and submit to the project team in a timely manner.

  • Communicate patient safety concerns and issues to the GCPM, GCPC, and investigator site as appropriate.

  • Perform assigned nursing tasks and lift equipment (up to 25lbs).

  • Ensure reliable transportation for DCVs and transport necessary supplies (e.g., centrifuge, ECG machine).

Qualifications:

  • Active, unencumbered RN licensure or certification in Canada.

  • Multistate practice/licensure preferred.

  • Minimum 2+ years of post-graduate nursing experience.

  • Clinical research experience preferred.

  • Basic Life Support (BLS) Certification.

Preferred Skills:

  • Strong verbal and written communication skills in English.

  • Flexible and adaptable to schedule and process changes with the ability to travel on short notice.

  • Experience with computer systems, MS Office, and Google applications.

  • Willingness to gain expertise in propriety eSource software.

  • Organized, able to multitask, and prioritize tasks based on protocol and visit requirements.

  • Prepared for specific visit requirements and troubleshooting at visits.

Additional Information:

  • Candidates must be legally eligible to work in Canada.

Workplace Commitment:

ProPharma values diversity, equity, and inclusion. We provide a safe and empowering workplace for employees to thrive, embracing innovative and entrepreneurial spirits. As an Equal Opportunity Employer, we ensure that all employees feel empowered to succeed.

Additional Notes:

  • ProPharma does not accept unsolicited resumes from recruiters or third-party agencies.

  • No phone calls or emails regarding this posting, please.