Travel Sub-Investigator

Overview

Travel Sub-Investigator role supporting clinical research studies through a mix of travel and remote tele-medicine work, administering investigational products and performing physical examinations beyond the standard clinical research Sub-Investigator role.

What you'll do

• Conduct study visits, perform physical exams, and administer investigational products (oral, IV, IM, SQ, transdermal).
• Perform phlebotomy, IV placement, vital signs, ECGs, and specimen collection/processing.
• Monitor participants throughout the study and educate participants on study medications.
• Provide direct clinical care and maintain a safe clinical environment.
• Ensure compliance with study protocols, GCP, SOPs, IRB requirements, OSHA standards, and applicable regulations.
• Review informed consent, protocol, and investigator brochure; complete and sign study documentation.
• Oversee delegated study activities and ensure accurate documentation.
• Assess and manage adverse events and infusion reactions; review laboratory and clinical data for medical significance.
• Provide medical management of study participants; evaluate eligibility, approve enrollment/randomization, and ensure timely reporting of serious adverse events to the Principal Investigator.
• Collaborate with the Principal Investigator and research team; communicate with study participants, sponsors, IRBs, and internal departments; attend meetings.
• Support subject recruitment, prescreening, scheduling, and coordination of study activities.
• Train and mentor clinical staff on study procedures; delegate responsibilities appropriately.
• Maintain clinical readiness; participate in quality improvement activities; complete required documentation and perform other assigned duties.

What you'll need

• Minimum education: at least a Master's level science degree.
• Nurse Practitioner or Physician Assistant with 5+ years of clinical experience.
• Active, unrestricted licensure in at least 10 U.S. states, and willingness to obtain additional state licenses as needed.
• Clinical practice experience with infusion skillset.
• 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 and 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.
• Strong verbal and written communication skills.
• Team collaboration skills; work effectively with other team members to accomplish mutual 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.
• Good management and organizational skills; understanding of medical procedures.
• Exceptional interpersonal skills and ability to work independently.
• Ability to lift a minimum of 50 pounds.
• Command of professional and business English (written and spoken).
• Authorization to work in the US for any employer, with no need for visa sponsorship now or in the future.
• Ability to live in the USA and travel with 24–36-hour notice.

Nice to have

• At least 1 year of relevant work experience as Sub-Investigator in a clinical research setting.
• At least 1 year of experience as a Clinical Research Coordinator, or willingness to learn.

Details

• On-site mixed with remote tele-medicine work position.
• Regional and nationwide travel up to 100% dependent on project design and business need; regularly planned travel required.
• Physical demands: use of keyboards and computer equipment; walking 10%, standing 30%, sitting 50%; lifting up to and overhead 25 lbs.
• Expected pay range $130,000 – $165,000 USD per year for full-time team members.