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 the US