- Performs nursingspecific tasks, as required by protocol, and towards the care andwell-being of study participants
- Confirms thatunit is prepared for upcoming studies, including preparation ofspecimen collection, inventory of medical supplies, and requiredequipment
- Explains protocol procedures toparticipants
- Responsible for the InformedConsent process; from initial informed consent and throughout allphases of study discusses study details with the participant inaccordance with ICH and FDA guidelines
- Performsstudy-related tasks and procedures, such as investigational productadministration, phlebotomy, urine collections, placement andmaintenance of IV catheters, vital signs, ECGs,etc
- Monitors and documents allparticipants' adverse events, medical conditions andresponses to study medications andtreatments
- Quality controls source documentsand other work regularly throughout each shift
- 12-hours shift (7am-7pm, 7pm-7am) -depends on Study schedule
- RNs to be flexible todo Dayshifts and Nightshifts, this doesn't mean you willflip around constantly, but once a while you may need to work theshifts which is not your preferred shift
- Oneweekend every 2 week
- BSN degreerequired
- MD State licenserequired
- 3 to 5 years of nursing experience ina hospital setting
- 1 year of clinical researchexperience is a plus
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Clinical Research Nurse - Dubai, United Arab Emirates - ClickJobs
Description
JobDescription
JobDescription
Pharmaron is a leading clinicalresearch company, and we are currently looking for a ClinicalResearch Nurses to join our team on a part-time basis in Baltimore,Maryland. The Clinical Research Nurse participates throughout theentire clinical trials study process.
As aResearch Nurse, you are responsiblefor a variety of clinical research activities, ensuring thatestablished protocols are followed, maintaining study protocolintegrity, monitoring participant's status and safety, andplaying a significant role in the training of clinicalstaff.
Schedule:
Qualifications: