Clinical Research Nurse Practitioner (APRN) or Physician Associate (PA-C)

Conquest Research is actively seeking a bilingual physician assistant (PA-C) or Nurse Practitioner (ARNP) to join our rapidly growing team. Your work will require providing patient-facing services at 2 free-standing clinical research sites (Winter Park and Lake Nona) focused on phase 2 and phase 3 clinical trials. The clinician will be working with a dedicated team of professionals and will serve as a Sub-Investigator clinician for the research sites, ensuring all elements of the studies are completed in compliance with standard operating procedures. The ability to be proficient in both speaking and writing in English and Spanish is required. Responsibilities include but are not limited to: Perform all study responsibilities in compliance with the approved protocol Participates in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements. Document all findings in subject specific source documents Perform physical examinations as part of screening evaluation and active study conduct Provide ongoing assessment of the study subject/patient to identify adverse events Provide medical management of adverse events as appropriate Communicate with sponsors and auditors as requested Possess a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form. Participate in on-call activities as required to ensure adequate medical coverage Delegate study responsibilities as appropriate to trained study staff Educate patients on health maintenance and respond to patient care inquiries Effectively work within a patient care team, including fellow Providers, Collaborative Physicians, Clinical Research Coordinators, Pharmacists, and other members of the health care team The Sub-Investigator may also perform all or some of the functions of the Principal Investigator and is responsible for performing study-related procedures and /or making important study-related decisions in compliance with the ethical conduct of the study These responsibilities include but are not limited to: General study coordination activities Review participant's inclusion and exclusion criteria Collect medical history Physical exams Collect vitals: body temp, pulse oximetry, respirations, heart rate, etc. Specimen collections and diagnostic assays Facilitate patient surveys and questionnaires Patient education Patient scheduling Treatment administration Required Qualifications Minimum of two years of medically relevant experience or equivalent Effective verbal, written, and electronic communication skills Initiative, problem solving ability, adaptability, and flexibility Ability to work effectively and collaboratively with a health care team Proficiency with information management and technology Capacity to collaborate with professional colleagues as necessary to provide quality care Ability to perform Basic Life Support (BLS) assistance, including but not limited to performing CPR and operating an Automated External Defibrillator (AED) Ability to commute between Winter Park site and Lake Nona site is required Bilingual in Spanish/ English is required Preferred Qualifications Prior experience with Clinical Research Prior experience with Phlebotomy Education Master's Degree level education Current National Board Certification State licensure

Job Type:

Full-time Pay:

$100,000.00 - $120,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Employee assistance program Health insurance Paid time off Vision insurance

Education:

Master's (Required)

Language:

Spanish (Required)

License/Certification:

Certified Nurse Practitioner (Preferred) Ability to

Commute:

Winter Park, FL 32789 (Required)

Work Location:

In person