Clinical Research Sub-Investigator (NP/PA)

Job Title: Clinical Research Sub-Investigator (Nurse Practitioner OR Physician Assistant)Job DescriptionAs 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.ResponsibilitiesOversee 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.Essential SkillsA Master's level Science Degree, Nurse Practitioner, or Physician Assistant with 5+ years of clinical experience.Clinical practice experience with an infusion skillset.Currently licensed in good standing in one or more states.A minimum of 1 year of relevant work experience as a Sub-Investigator in a clinical research setting.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.Additional Skills & QualificationsAt least one year of experience as a Clinical Research Coordinator or willingness to learn.Strong team collaboration skills and a positive attitude.Ability to balance tasks with competing priorities.Critical thinking and problem-solving skills.Curiosity and a passion for learning, with the ability to take thoughtful risks while communicating concerns.Good management and organizational skills.Exceptional interpersonal skills and the ability to work independently.Ability to lift a minimum of 50 lbs.Work EnvironmentThis 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.Job Type & LocationThis is a Contract position based out of Tyler, TX.Pay and BenefitsThe pay range for this position is $58.00 - $73.00/hr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Tyler,TX.Application DeadlineThis position is anticipated to close on Mar 27, 2026.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our peopleActalent is an equal opportunity employer.About ActalentActalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC-with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.