CenExel
Psychiatric Clinical Research RN (Day Shift)
Join CenExel as a Psychiatric Clinical Research RN (Day Shift). This role focuses on overseeing the daily clinical study activities, serving as a liaison between the investigative site and the Sponsor, and accurately documenting all information throughout the clinical research process. About Us
CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence are renowned and long‑standing, with specialty areas including Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We have in‑patient capability and a history of success in complex early‑phase trials. Shift
Monday, Tuesday, Wednesday, 6 am – 6 pm. Essential Responsibilities and Duties
Provides general nursing care to study participants as necessary, including monitoring vitals, lab tests, and other assessments. Reviews and executes clinical research protocols. Maintains study documents in accordance with sponsor and site requirements. Recruits potential study subjects and screens subjects for eligibility. Completes and maintains Case Report Forms per protocol. Accompanies sponsor representatives during visits and maintains effective communication with the sponsor. Maintains adequate inventory of all data and supplies. Regularly attends training, staff, initiation, study start‑up, and other meetings as assigned. Observes, documents, reports, and follows up on adverse events and serious adverse events. Conducts the informed consent process per CenExel Standard Operating Procedures. Follows up on laboratory results and maintains safety standards. Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens. Assists with quality assurance activities, completes queries, and obtains necessary signatures. Oversees or coordinates the 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 best practices, FDA Code of Federal Regulations, ICH, GCP, CenExel standard operating procedures, site working practices, protocol, and company guidelines. Assumes other duties and responsibilities as assigned. Education, Experience, and Skills
Registered Nurse with a current state license and no disciplinary action. BLS or ACLS certification or ability to obtain. 1+ years of experience required. IV certification required, depending on site. Capable of performing all clinical tasks relevant to licensure and/or training. Excellent verbal and written communication skills. Strong interpersonal skills with patients, staff, and sponsor representatives. Self‑motivated and able to perform tasks independently. Calm and effective in emergency situations. Professional image that upholds company vision. Working Conditions
Indoor clinic environment. Sitting, typing, standing, and walking required. Lightly active position; occasional lifting up to 20 pounds. On‑site work arrangement. CenExel 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.
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Join CenExel as a Psychiatric Clinical Research RN (Day Shift). This role focuses on overseeing the daily clinical study activities, serving as a liaison between the investigative site and the Sponsor, and accurately documenting all information throughout the clinical research process. About Us
CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence are renowned and long‑standing, with specialty areas including Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We have in‑patient capability and a history of success in complex early‑phase trials. Shift
Monday, Tuesday, Wednesday, 6 am – 6 pm. Essential Responsibilities and Duties
Provides general nursing care to study participants as necessary, including monitoring vitals, lab tests, and other assessments. Reviews and executes clinical research protocols. Maintains study documents in accordance with sponsor and site requirements. Recruits potential study subjects and screens subjects for eligibility. Completes and maintains Case Report Forms per protocol. Accompanies sponsor representatives during visits and maintains effective communication with the sponsor. Maintains adequate inventory of all data and supplies. Regularly attends training, staff, initiation, study start‑up, and other meetings as assigned. Observes, documents, reports, and follows up on adverse events and serious adverse events. Conducts the informed consent process per CenExel Standard Operating Procedures. Follows up on laboratory results and maintains safety standards. Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens. Assists with quality assurance activities, completes queries, and obtains necessary signatures. Oversees or coordinates the 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 best practices, FDA Code of Federal Regulations, ICH, GCP, CenExel standard operating procedures, site working practices, protocol, and company guidelines. Assumes other duties and responsibilities as assigned. Education, Experience, and Skills
Registered Nurse with a current state license and no disciplinary action. BLS or ACLS certification or ability to obtain. 1+ years of experience required. IV certification required, depending on site. Capable of performing all clinical tasks relevant to licensure and/or training. Excellent verbal and written communication skills. Strong interpersonal skills with patients, staff, and sponsor representatives. Self‑motivated and able to perform tasks independently. Calm and effective in emergency situations. Professional image that upholds company vision. Working Conditions
Indoor clinic environment. Sitting, typing, standing, and walking required. Lightly active position; occasional lifting up to 20 pounds. On‑site work arrangement. CenExel 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.
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