Registered Nurse - Clinical Research (12:00am - 8:30am)

ABOUT US

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country.

Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.

Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

HOURLY RANGE / SCHEDULE

$39.00 - $41.00 (Depending on Experience) + $3 / hr differential pay (After 90 days)

Wednesday - Sunday (12 : 00am - 8 : 30am)

Why CenExel ACT?

• Be part of one of the largest and fastest-growing clinical research companies in the United States with potential internal growth and advancement
• Work alongside a successful and dynamic team conducting clinical trials for new medications and treatment in various therapeutic areas not limited to psychiatric, general health, and neurological phase I-IV studies
• Great benefits and perks

With continuous growth at CenExel ACT , we are looking to fill our vacant Registered Nurse position. We would love to speak to you if you have :

• Must be able to effectively communicate verbally and in writing.
• Must be a Registered Nurse with a current license in CA.
• Must be capable of performing all clinical tasks relevant to licensure and / or training.
• Must be able to clearly communicate verbally with patients.
• Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
• Must be self-motivated and able to perform tasks independently.
• Ability to react calmly and effectively in emergency situations.
• Must reflect the professional image of the company, upholding the company vision in actions and demeanor.

DUTIES AND RESPONSIBILITIES

• Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
• Reviews and executes clinical research protocols.
• Completes and maintains study documents in accordance with sponsor and site requirements.
• Possible recruitment of potential study subjects.
• Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
• Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
• Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
• Maintains adequate inventory of all data and supplies.
• Regularly attends training meetings, staff meetings, initiation meetings, 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 CenExel Standard Operating Procedures.
• 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 (if applicable) of laboratory specimens.
• Is on call to answer questions for other members of support staff, study patients or other medical staff, as necessary.
• Assists with quality assurance activities and completes queries, as applicable.
• Obtains Principal Investigator signatures on necessary documents.
• 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.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

We offer a competitive pay package which include but not limited to :

• PTO / Holiday
• Medical / Dental / Vision
• 401(k) / Dependent Care FSA / EAP
• Ancillary Benefits / Group Life Insurance / AD&D
• Employee Discount Program

WORKING CONDITIONS

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

CenExel ACT is an equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status regarding public assistance, veteran status, or any other characteristic protected by federal, state or local law.