Clinical Research Nurse Jobs

About The Position

Requirements

• Current Registered Nurse license in California.
• Ability to perform clinical tasks relevant to licensure and/or training.
• Ability to communicate clearly with patients verbally.
• Good interpersonal skills in interactions with patients, staff, and sponsor representatives.
• Self-motivated and able to perform tasks independently.
• Ability to react calmly and effectively in emergency situations.
• Professional conduct that reflects the company’s image and vision.
• Must be available to work weekends.
• Must be available to work an AM shift during a 2–3 week training period.
• Ability to perform the essential physical activities of sitting, typing, standing, and walking, and occasional lifting of up to 20 pounds.
• Ability to report to work as scheduled.

Responsibilities

• Provide general nursing care to study participants, including monitoring vital signs and blood sugar and conducting lab tests.
• Review and execute clinical research protocols.
• Complete and maintain study documents in accordance with sponsor and site requirements.
• Recruit potential study subjects when applicable.
• Screen subjects for eligibility and schedule study-specific assessments as designated on the Delegation of Authority Log.
• Complete and maintain Case Report Forms in agreement with source documentation and study protocols.
• Accompany sponsor representatives during visits and maintain effective ongoing communication with sponsors.
• Maintain adequate inventory of data and supplies.
• Attend training, staff, initiation, study start-up, and other assigned meetings.
• Observe, document, report, and follow up on adverse events and serious adverse events.
• Conduct the informed consent process according to CenExel Standard Operating Procedures.
• Follow up appropriately on laboratory results.
• Maintain safety standards while performing job responsibilities.
• Maintain study logs and site relations.
• Ensure proper collection, processing, and shipment of laboratory specimens when applicable.
• Be on call to answer questions from support staff, study patients, or other medical staff as necessary.
• Assist with quality assurance activities and complete queries as applicable.
• Obtain Principal Investigator signatures on necessary documents.
• Oversee or coordinate investigational medication administration and follow subjects throughout their study stay according to protocol.
• Ensure accountability and adequate supply of study and clinical drugs.
• Perform other duties and responsibilities as assigned.

Benefits

• Health insurance
• Dental insurance
• Vision insurance
• Long-term disability insurance
• Short-term disability insurance
• Life insurance
• 401(k)