Propharmagroup
Registered Nurse-Clinical Trial-Tracy, CA
United States
Work authorization requiredDetected 21 days ago
GCPProduct ManagementClinical TrialsClinical ResearchPharmacovigilanceResearchMicrosoft Office
About the role
- Provides quality DCV services to patients at a location outside of the investigator site (e.g., home, office, school).
- 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.
Responsibilities
- Collaborates with Director of Nursing and GoClinical Clinician Manager to apply clinical research and nursing practices to develop solutions to complex problems.
- 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.).
- 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 partners with its clients through an advise-build-operate model across the complete product lifecycle.
- We celebrate our differences and strive to create a workplace where each person can be their authentic self.
- We do not rely on AI screening tools to support our hiring process.
Requirements
- Minimum 2+ years post-graduate experience
- Ability to communicate in English (both verbal and written).
- Working knowledge of MS Office suite and Google applications.
- Willingness to gain expertise in the use of propriety eSource software.
- All candidates must be legally eligible to work in the US
- Education & Experience
- Active, unencumbered RN licensure or certification in US
- Basic Life Support (BLS) Certification
- 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:
Nice to have
- Multistate practice/licensure preferred where applicable
- Clinical research experience preferred
- Preferred Skills
- Ability to work afterhours or weekends preferred.
Benefits
- We are committed to diversity, equity, and inclusion.
- Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.
Equal opportunity
- With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
- Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
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This listing is sourced directly from Propharmagroup's careers page and normalized into a canonical job model.