Clinical Research RN

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About Us
Cen Exel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. All sites have inpatient capability and a history of success.

Job Summary
With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities, serving as a liaison between the investigative site and the Sponsor, and accurately and ethically documenting all information obtained throughout the clinical research process.

Schedule
Monday – Friday 8 am – 4:30 pm

Essential Responsibilities and Duties

• Provides general nursing care to study participants, including monitoring vitals, blood sugar, lab tests.
• Reviews and executes clinical research protocols.
• Completes and maintains study documents in accordance with sponsor and site requirements.
• Recruitment and screening of potential study subjects.
• Schedules subjects for study specific assessments as designated on the Delegation of Authority Log.
• Completes and maintains Case Report Forms according to study protocol.
• Accompanies sponsor representatives during visits and maintains effective communication.
• Maintains adequate inventory of all data and supplies.
• Regularly attends training meetings, staff meetings, initiation, study start-up meetings, and other meetings as assigned.
• Observes, documents, reports, and follows up on adverse events and serious adverse events.
• Conducts the informed consent process per Cen Exel SOPs.
• Follows up appropriately on all laboratory results.
• Maintains safety standards when performing job responsibilities.
• Maintains study logs and site relations.
• Ensures proper collection, processing, and shipment of laboratory specimens.
• Assists with quality assurance activities and completes queries.
• Obtains Principal Investigator signatures on necessary documents.
• Oversees or coordinates administration of investigational medication and follows subjects throughout the study stay per protocol.
• Ensures accountability and adequate supply for study and clinical drugs.
• Supports strict adherence to FDA regulations, ICH, GCP, Cen Exel SOPs, and company policies.

Education / Experience / Skills

• Registered Nurse with a current license in the state in which the employee will be working and no disciplinary action on the license.
• BLS or ACLS certified or able to obtain.
• 0–1 year of experience required.
• IV certified, depending on site.
• Capable of performing all clinical tasks relevant to licensure and/or training.
• Clear verbal communication with patients.
• Good interpersonal skills demonstrated through 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 image of the company, upholding company vision in actions and demeanor.
• Effective verbal and written communication.

Working Conditions

• Indoor clinic environment.
• Essential physical requirements include sitting, typing, standing, and walking.
• Lightly active position, occasional lifting up to 20 pounds.
• Reporting to work, as scheduled, is essential.
• On‑site work arrangement.

Cen Exel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.