Nurse Practitioner - Must be bilingual (English/Spanish)

Alcanza Clinical Research; Town of Florida (NY); On-site; USD 85,000 - 105,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) plan with a safe harbor match

Job summary

A clinical research organization is seeking a Nurse Practitioner to assist as a Sub-Investigator in research studies. Responsibilities include conducting assessments, ensuring patient safety, and coordinating clinical activities. Candidates should possess a Bachelor's degree, 2 years of clinical experience, and an active professional license. Research experience and BLS/ACLS certification are preferred. The position also offers a range of benefits for full-time employees, including health and retirement plans.

Qualifications

• Minimum of 2 years of clinical experience.
• One year of research experience is highly preferred.
• Bilingual (English/Spanish) proficiency is a plus.

Responsibilities

• Perform functions of Sub-Investigator on research studies under the Principal Investigator's direction.
• Monitor patient status and safety; collect and organize research data.
• Participate at pre-study and site initiation visits.

Skills

Proficiency with computer applications

Basic clinical procedures

Strong organizational skills

Written and verbal communication skills

Interpersonal skills

Integrity and dependability

Education

Bachelor’s degree

Active license as an advanced practice professional

BLS/ACLS certification

Job description

Alcanza is a growing multi‑site, multi‑phase clinical research company with locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have a strong presence across Phase I‑IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

Department: Operations

Location: Innovation - Palmetto Bay, FL

Position Overview

The Nurse Practitioner will be assigned as a Sub‑Investigator in research studies. As delegated by the Principal Investigator (PI), the NP will perform physical and medical history assessments and assist the PI with medical management of subjects on a trial. The Sub‑Investigator may also function in a Clinical Research Coordinator role and coordinate daily clinical research activities according to the organization’s SOPs, GCP, and FDA/ICH guidelines.

Key Responsibilities

• Under the direction of the Principal Investigator, perform the functions of Sub‑Investigator on research studies. Ensure IRB‑approved protocols are implemented and followed.
• Execute the informed consent process and monitor patient status and safety; collect and organize research data; schedule and conduct study‑specific training and site in‑services to study‑related staff on new or amended protocols; educate patients and their families about treatments and possible side effects.
• Ensure and protect the patient’s welfare and rights as a research subject.
• Perform research protocol procedures which may include, but are not limited to: physical exams, injections, IVs, medical history review and assessment, and assessments of vital signs, laboratory results and adverse events. May mix and/or dispense investigational product and instruct subjects on usage and potential drug interactions.
• Participate at pre‑study and site initiation visits, investigator meetings, and other customer‑facing meetings, as needed.
• Assist site management with support in change management and process improvement.
• Assist and participate with new staff training and mentoring.
• Assist and guide employees on study‑specific tasks.
• Utilize and ensure the appropriate equipment is on‑site for Universal Precautions for themselves and others in and around areas that may contain potential biohazards.
• Work with the Principal Investigator to maintain high quality and patient safety.
• Establish rapport with sponsor representatives and maintain frequent face‑to‑face, written and telephone contact with various persons involved in the study, including but not limited to the patients, relatives/friends of the patients, doctors, pharmaceutical sponsors and all levels of the company.
• May perform role of Clinical Research Coordinator on studies as needed.
• Maintain strict confidentiality of patients, employees and company information at all times and adhere to HIPAA Guidelines.
• Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study.
• Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs and maintain ongoing regulatory documents.
• Practical knowledge of document processes and reporting of SAEs, 1572s, CRFs, ICFs, etc.
• Maintain accountability of own ongoing professional growth and development.
• Perform all other duties as requested or assigned.

Minimum Qualifications

A bachelor’s degree and a minimum of 2 years of clinical experience, or an equivalent combination of education and experience is required. An active license (in good standing) to practice as an advanced practice professional in the state of practice is required. One year of research experience is highly preferred. BLS/ACLS certification is required. Bilingual (English/Spanish) proficiency is a plus.

Required Skills

• Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications.
• Ability to type proficiently (40+ wpm).
• Perform basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, reconstitution of IP, injections, and IVs.
• Strong organizational skills and attention to detail.
• Well‑developed written and verbal communication skills.
• Well‑developed interpersonal and listening skills and the ability to work well independently as well as with co‑workers, subjects, managers and external customers.
• Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
• Must be professional, respectful of others, self‑motivated, and have a strong work ethic.
• Must possess a high degree of integrity and dependability.
• Ability to work under minimal supervision, identify problems and implement solutions.
• Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits

• Full‑time employees regularly scheduled to work at least 30 hours per week are benefits‑eligible, with coverage starting on the first day of the month following date of hire.
• Medical, dental, vision, life insurance, short and long‑term disability insurance, health savings accounts, supplemental insurances, and a 401(k) plan with a safe harbor match are offered.