Registered Nurse

at  Cliantha Research Ltd

QUALIFICATIONS:

• Licensed and in good standing with the College of Nurses of Ontario
• Currently hospital employed in acute care
• Intensive care unite, coronary care unit or emergency department experience
• 1 year clinical practice with assessment skills
• Current CPR certification required
• Advanced Cardiac Life Support (ACLS) or other emergency experience desired
• Ability to respond to study participant needs (i.e. lifting, crouching, bending, etc.)
• Ability to recognize inconsistencies or abnormalities
• Professional and positive attitude
• Effective trouble-shooting and decision making skills, able to escalate response to situations when relevant
• Proven solid project planning/ coordination/ management skills
• Strong analytical and problem solving skills
• Excellent organizational skills, detail oriented, efficient and able to multi-task and prioritize effectively
• Excellent interpersonal skills
• Strong written and verbal communication skills
  Job Type: Part-time

Schedule:

• 8 hour shift

Education:

• Bachelor’s Degree (preferred)

Experience:

• Registered Nurse: 2 years (required)

Licence/Certification:

• Registered Nurse (RN) License in Province of Ontario (required)

Work Location: In perso

• Monitor the ongoing safety of Study Participants in house
• Assist in the overall conduct of clinical studies for BE and Phase 1-4 studies including, but not limited to:
• Execution of all aspects of study visits as experience and training allow
• Perform clinical and study procedures as per study protocols, ensuring minimal deviations and proper tracking and reporting when deviations occur
• Interact with Principal Investigator, sponsor, manager and Scientific Director and other study coordinators to ensure all aspects of protocols and study requirements are understood
• Assist in design, implementation and coordination of all aspects of data collection, source documentation and CRF transcription as per protocol, SOPs and ICH/GCP guidelines
• Data entry as required
• Participate in development and execution of Quality Control processes
• Prepare for and support QA audits and sponsor monitoring visits
• Study drug management
• IRBs interactions
• Work with study managers and other members of the study teams to ensure study performance meets or exceeds client expectations
• Participate in Operational kick-off meetings and regular study update meetings
• Ensure study subjects are having the best possible experience while participating in studies conducted at Cliantha Research.
• Assist in development of department SOPs, Equipment Binders, templates; Nurse specific
• Procurement of equipment and supplies as required; Nurse specific
• Participate in training of staff as experience and qualifications permit
• Able to implement and execute emergency measures
• Responsible for adverse drug experience assessment, evaluation, collaboration of medical care, documentation and follow-up during study conduct or until resolution
• Report abnormal vital signs or unusual adverse events of study participants
• Certified to preform and train all nursing tasks (vitals, ECGs, blood draws, etc.)
• Assist in the design of study and time/ event schedules involving special medical procedures
• Input into safety of study design
• Other clinical procedures as necessary
• Certified to preform, monitor and/or train invasive and non-invasive dosing procedures
• Oversee and coordinate contract nurse/ paramedic training
• Train clinic associates on ECG procedures, manual vital procedures, and assessment skills related to reporting adverse events
• May administer Informed Consent Forms
• Other safety duties as assigned
• Participate in Environmental Chamber validations and maintenance; write validation protocols and reports, conduct validation experiments, maintain appropriate logbooks as needed
• Assist in all aspects of company start up activities as required
• Assist in set up and maintenance of laboratory and EMS system
• Ensure study subjects are having the best possible experience while participating in studies conducted at Cliantha Research.
• Ability to demonstrate authority; troubleshoot situations; and make quick, accurate decisions under pressure
• Capable of representing the company in a professional manner
• Model the core values, policies, and procedures for Cliantha
• Uphold the company mission statement and conduct yourself at all times in a respectful and business-like Be a positive role model for all staff and interact with colleagues in a collaborative way.
• Execute other duties as may be required