Executive Director, Investigator Development / Sub-Investigator

🔥 0 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🔴 Lead

👔 Director

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ObjectiveHealth

WebsiteLinkedInAll Job Openings

201 - 500 employees

🏥 Healthcare

💼 Consulting

⚕️ Healthcare Insurance

💰 $7M Venture Round on 2022-11

Healthcare • Consulting • Healthcare Insurance

ObjectiveHealth is a healthcare company dedicated to integrating clinical trials into standard medical practice, particularly at the point of care. Specializing in areas such as gastroenterology, dermatology, urology, oncology, and metabolism disorders, ObjectiveHealth offers a unique technological platform that facilitates patient enrollment, screening, and trial management. By partnering with physicians and community health centers, the company enhances patient access to advanced clinical trials, providing sponsors with a robust research infrastructure. ObjectiveHealth also strives to improve patient outcomes through its innovative use of electronic health records and health algorithms to find suitable patients for trials and optimize trial results.

📋 Description

• Partner with executive leadership to identify and develop future Investigators and research providers • Engage with new and emerging investigators to explain investigator responsibilities, expectations, and time commitments • Lead training and mentorship programs for new Principal Investigators and Sub-Investigators • Assess investigator readiness and provide individualized mentoring for clinical trial conduct • Facilitate mentoring on sponsor requirements and emerging industry best practices • Serve as a subject matter expert in clinical research regulations, investigator responsibilities, and GCP compliance • Advise investigators on protocol interpretation, study procedures, eligibility assessments, and participant management • Support investigators with CRIO • Participate in sponsor visits, Site Initiation Visits, monitoring visits, audits, and regulatory inspections as needed • Support and perform patient care activities, including informed consent, physical assessments, blood draws, specimen handling, medication administration, FibroScans, ECGs, and other protocol-required procedures • Investigate, track, and report Adverse Events and Serious Adverse Events as instructed by study sponsors • Monitor investigator effectiveness using performance metrics, quality indicators, audit findings, and compliance outcomes • Identify and implement updates to SOPs and policies affecting investigator roles and operational requirements • Attend investigator meetings and study-related training sessions required by sponsors • Review scientific literature and participate in continuing education, industry conferences, and seminars

🎯 Requirements

• Must hold and maintain licensure as a Physician Assistant or Nurse Practitioner • Willingness to obtain and maintain multi-state licensure as appropriate • Prior experience in clinical research, preferably in a clinical role • At least two years of experience in industry-funded clinical research • Experience serving as a Sub-Investigator for Phase 2–3 clinical trials • Experience with EMR and/or EDC systems • Knowledge of biological and medical terminology • Ability to travel up to 40% • Legal authorization to work in the United States • Work visas are not currently accepted