Remote Travel Sub-Investigator

Summary

Join our team as a Sub-Investigator at Care Access, where you will be responsible for supporting clinical research studies through travel and remote tele-medicine work. As a highly motivated Nurse Practitioner or Physician's Assistant, you will oversee the execution of study protocols, administer investigational products, and perform physical examinations.

Requirements

• 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
• Excellent working knowledge of federal regulations, good clinical practices (GCP)
• Ability to communicate and work effectively with a diverse team of professionals
• Strong organizational skills: Able to prioritize, support, and follow through on assignments with good understanding of medical terminology
• Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors
• Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals
• Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
• Ability to balance tasks with competing priorities
• Critical thinker and problem solver
• Curiosity and passion to learn, innovative, and able to take thoughtful risks while communicating concerns and mitigations
• Good management and organizational skills, understanding of medical procedures
• Exceptional interpersonal skills, willingness to the ability to work independently
• Ability to lift a minimum of 50 pounds
• Command of professional and Business English (written and spoken)

Responsibilities

• Work closely with the Principal Investigator to oversee the execution of study protocols
• Delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols
• Read and understand the informed consent form, protocol, and investigator's brochure
• Be available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visit
• Sign and ensure that the study documentation for each study visit is completed
• Perform all study responsibilities in compliance with the IRB approved protocol
• Administration of Investigational Products (via subcutaneous, transdermal, intramuscular, intravenous, or oral routes)
• Proficiency in starting, monitoring, and maintaining intravenous lines
• Contribute as an active member of clinician team involved in the management of infusion or other investigational product related reactions
• Maintain a clean, efficient clinical area to assure the highest standards of patient care
• Follow safety and PPE procedures as well as maintain proper documentation of infusion procedures
• Timely communications with internal teams, investigators, review boards, and study subjects
• Perform trial procedures as per delegation which can include the following but not limited to
• Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling screening appointment
• Obtain informed consent per SOP
• Administer delegated study questionnaires, as appropriate
• Collect and evaluate medical records
• Complete visit procedures and ensure proper specimen collection, processing, and shipment in accordance with protocol
• Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc
• Review screening documentation and approves subjects for admission to study
• Review admission documentation and approves subject for randomization
• Provide ongoing assessment of the study subject/patient to identify Adverse Events
• Ensure that serious and unexpected adverse events are reported promptly to the Pl
• Review and evaluates all study data and comments to the clinical significance of any out-of-range results
• Perform physical examinations as part of screening evaluation and active study conduct
• Provide medical management of adverse events as appropriate
• Dispense study medication per protocol and/or IVRS systems. Educate patient on proper administration and importance of compliance
• Monitor patient progress on study medication

Benefits

• PTO/vacation days, sick days, holidays
• 100% paid medical, dental, and vision Insurance. 75% for dependents
• HSA plan
• Short-term disability, long-term disability, and life Insurance
• Culture of growth and equality
• 401k retirement plan