Clinical Research Nurse

Evolution Research Group; Lemon Grove (CA); On-site; USD 51,000 - 58,000; Full time

Benefits offered by this job

Medical & dental coverage

401(k) match

Paid time off

Job summary

Evolution Research Group is seeking a Clinical Research Nurse in Lemon Grove, CA. This full-time role involves performing clinical duties, data collection, and patient care within a multi-disciplinary team across Phase I–IV trials.

Must hold RN licensure with ACLS and be able to manage protocol requirements in a fast-paced environment. The position emphasizes administering study drug, informed consent, safety monitoring, and compliance with GCP/ICH guidelines.

Qualifications

• RN licensure in the applicable state with ACLS certification.
• Clinical research experience preferred but not required.
• Excellent communication and multitasking skills.
• Ability to work in a fast-paced clinical trial setting.

Responsibilities

• Perform study events and collect data per protocol.
• Administer study drug as assigned.
• Assist medical personnel with participant care duties.
• Discuss and obtain Informed Consent as assigned (site dependent).
• Notify staff of abnormal results and adverse events.
• Maintain safety and well-being of study participants.
• Maintain telemetry and ECG proficiency.

Skills

RN licensure

ACLS certification

Excellent communication

Regulatory knowledge

Education

RN licensure (state)

ACLS certification

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Nurse

Full Time Lemon Grove, CA, US

2 days ago Requisition ID: 1471

Salary Range: $37.00 To $42.00 Hourly

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us:

We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Registered Nurse will perform a variety of activities related to the clinical area, including medical support systems and assisting medical personnel with study participants care duties as assigned. Incumbents work under supervision of clinical staff, performing routine duties and primarily, referring questions and problems to the Clinical Research Coordinator assigned to study or the PI.

Responsibilities:

Clinical:

• Perform study events and collects clinical data as per protocol requirements.
• Administer study drug as assigned.
• When assigned, serve as Pharmacy Staff.
• Discuss and administer Informed Consent Form, as assigned (dependent on site)
• Notify appropriate staff of abnormal results while collecting data, adverse events, or unusual incidents.
• Assure minimal discomfort for study participants while performing all duties.
• Working knowledge of telemetry monitoring and interpretation of tracings
• Maintain safety and well-being of study participants during assigned shift.
• Knowledge of Holter monitor skills.
• Prepare participants for events.
• Understand all functions of telemetry monitoring machine.
• Collect all telemetry tracings for licensed personnel to review.
• Ability to use proper advanced life support equipment and supplies.
• Maintain skills in the use of ECG machine, taking accurate vital signs and IV insertion.
• Keep apprised of all new OSHA, BLS, ACLS and GCP/ICH rules, regulations, and procedures.
• Perform initial evaluation of adverse event.
• Knowledge of drug reactions and the synergistic effects of drugs combined with other medicines.
• Ability to apply basic principles of mathematics to the calculation of problems associated with medication dosages.
• Must be capable of providing advanced life support emergency medical services, including conducting of and interpreting ECGs, electrical interventions to support cardiac functions, performing advanced endotracheal intubations in airway management and relief of pneumothorax and administering of appropriate intravenous fluids and drugs under direction of a designated physician.
• Stay focused while assuming the leadership role inherent in carrying out the functions of the position.
• Provide top quality care and concurrently handle high levels of stress.

Administrative:

• Read and understand each protocol in which he/she is involved.
• Maintain knowledge and understanding of SOP for data collection.
• Maintain accurate and neat documentation records as required by the protocol.
• Follow proper safety procedures and report to supervisor immediately all injuries, unsafe practices, and unusual incidents.
• Know OSHA and GCP/ICH rules and regulations and comply with all requirements.
• Perform inventory of supplies needed and report deficiencies to clinical staff supervisor.
• Stay on duty/assigned shift until relieved by oncoming staff.

Educational:

• Maintain current licensure, registration and/or certification within educational background.
• Maintaincurrent BLS and/or ACLS certification
• Maintain necessary CEU’s for licensure, registration and/or certification.
• Assist in training new Paramedics, Emergency Medical Technicians (EMT), Medical/ Nursing Assistants (MA, NA) and Phlebotomy Technician
• Actively participatein ongoing Quality Assurance Program, HIPAA, and Compliance Programs
• Keepapprised of all new OSHA and GCP/ICH Rules and Regulations
• Attend all appropriate team meetings regarding study protocols.
• Learn and maintain skills in use of EKG machines and taking accurate vital signs.
• Read and understand site policy and procedures manuals, SOP manual, and employee handbook.

Additional Responsibilities:

• Comply with all site policies and procedures, especially those regarding protocol confidentiality.
• Demonstrate a caring, professional attitude and behavior toward study participants and staff, actively contributing to the well-being and dignity of the clinic.
• Maintain an overall good work attitude, promoting cooperation and professionalism and interactions with other staff members.
• Maintain assigned work areas in a clean, safe condition, and report any potential hazards immediately.
• Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

• Education and experience
  • Licensure as a Registered Nurse (RN) in the applicable state with ACLS Certification and a minimum of one year experience as an
  • RN in a medical facility
  • Clinical Research experience preferred but not required.
  • ACLS certification required.
• Requirements
  • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Knowledgeable in medical terminology
  • Good organizational and interpersonal skills
  • Attention to detail.
  • Excellent communication skills (interpersonal, written, verbal)
  • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as RealTime)