Sub Investigator

Benefits

Qualifications

• •A Master's level Science Degree, Nurse Practitioner with 5+ years of clinical experience
• •Clinical practice experience with an infusion skillset
• •Currently licensed in good standing in one or more states
• •Ability to check, perform, and document vitals as well as EKG (ECG)
• •Phlebotomy and expert IV skills
• •Excellent working knowledge of medical and research terminology
• •Strong organizational and communication skills
• •Ability to work effectively with a diverse team
• •Strong computer skills with experience using clinical trials databases, IVR systems, electronic data capture, MS Word, and Excel
• •Maintaining an inclusive environment through persistent self-reflection
• •7 more items(s)

Responsibilities

• •As a Sub Investigator, you will work closely with the Principal Investigator to oversee the execution of study protocols and ensure site compliance with various regulatory standards
• •You will be responsible for maintaining the highest standards of patient care and safety, while also contributing to the successful management of clinical trials
• •Oversee the execution of study protocols, delegating study-related duties to site staff, and ensuring compliance with Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and other relevant regulations
• •Participate in meetings with the director, other managers, and staff as necessary
• •Read and understand the informed consent form, protocol, and investigator's brochure
• •Be available for virtual or in-person consultations with subjects, addressing their questions and resolving medical issues during study visits
• •Complete and sign study documentation for each study visit
• •Administer investigational products via various routes, including subcutaneous, transdermal, intramuscular, intravenous, or oral
• •Perform proficiency in starting, monitoring, and maintaining intravenous lines
• •Contribute to the management of infusion or other investigational product-related reactions
• •Maintain a clean and efficient clinical area
• •Follow safety and PPE procedures, maintaining proper documentation of infusion procedures
• •Communicate timely with internal teams, investigators, review boards, and study subjects
• •Perform trial procedures as per delegation, including pre-screening study candidates, obtaining informed consent, administering questionnaires, collecting and evaluating medical records, and ensuring proper specimen collection
• •Train others and complete basic clinical procedures
• •Review screening and admission documentation, approving subjects for study participation and randomization
• •Provide ongoing assessment of study subjects to identify and manage adverse events
• •Evaluate study data for clinical significance and perform physical examinations as part of study conduct
• •Dispense study medication per protocol, educate patients on administration, and monitor progress
• •Other duties as assigned
• •This position requires working 5 days on-site
• •You will be part of a dynamic team in a fast-paced environment, contributing to cutting-edge clinical research
• •Building a culture of care, engagement, and recognition with clear outcomes
• •20 more items(s)