Registered Nurse-Clinical Trial-New Glasgow, Nova Scotia CAN

ProPharma; Windsor; Hybrid; CAD 70.000 - 95.000; Vollzeit

Zusammenfassung

ProPharma is seeking qualified nursing professionals to perform data collection visits (DCVs) for clinical studies across Canada. The role requires active RN licensure in the US with current BLS and the ability to travel to patient sites such as homes, offices, or clinics.

Responsibilities include completing study-specific trainings, ensuring Good Documentation Practices, and coordinating with project teams.

Qualifikationen

• Active, unencumbered RN licensure or certification in US
• Multistate practice/licensure preferred where applicable
• Minimum 2+ years post-graduate experience
• Clinical research experience preferred
• Basic Life Support (BLS) Certification

Aufgaben

• Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training.
• Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school).
• Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems.
• Completes source documentation during DCVs following Good Documentation practice and submits source to project team in a timely manner.
• Communicates issues and patient safety concerns to GCPM, GCPC, and investigator site as appropriate.
• Physically able to perform assigned nursing tasks and lift equipment up to 25lbs in weight.
• Access to a reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).

Kenntnisse

English communication

Travel readiness

Multitasking

Organized

Ausbildung

RN licensure in US

BLS Certification

Multistate licensure

Tools

MS Office

Google applications

Proprietary eSource software

Jobbeschreibung

Key Responsibilities:

• Completes study-specific requirements for each assigned study which may include GCP training, IATA (dangerous goods) training, and study-specific training.


• Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school).


• Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems.


• Completes source documentation during DCVs following Good Documentation practice and submits source to project team in a timely manner.


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


• Physically able to perform assigned nursing tasks and lift equipment up to 25lbs in weight.


• Access to a reliable transportation to perform DCVs and transport necessary supplies and equipment (e.g., centrifuge, ECG machine, etc.).

Qualifications:

• Education & Experience


• Active, unencumbered RN licensure or certification in US


• Multistate practice/licensure preferred where applicable


• Minimum 2+ years post-graduate experience


• Clinical research experience preferred


• Basic Life Support (BLS) Certification

Preferred Skills:

• Ability to communicate in English (both verbal and written).


• Flexible and able to make quick accommodations to schedule changes as well as process changes and to travel with limited notice. Ability to work afterhours or weekends preferred.


• Computer skills/experience. Working knowledge of MS Office suite and Google applications. Willingness to gain expertise in the use of propriety eSource software.


• Organized and able to multitask; prioritizes based on protocol and visit parameters.


• Consistent preparedness for specific visits requirements as well as equipment and additional supplies for potential trouble shooting at the visit.

Additional Information:

All candidates must be legally eligible to work in Canada

Our Culture and Commitment to Equality:

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you’re successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.

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