What are the responsibilities and job description for the Principal Investigator (PRN)/ $5,000 SIGN ON BONUS position at Future Med Clinical Research?
Future Med Clinical Research is a growing clinical research site in the Dallas area focused on delivering high-quality, patient-centered clinical trials. We are building a strong foundation to support multiple therapeutic areas and are seeking a motivated Principal Investigator to join us in a flexible, PRN capacity.
This is a unique opportunity to be part of a developing research site with the ability to grow into a long-term leadership role as the site expands.
The PI leads participant safety, study integrity, and regulatory compliance, performing evaluations, reviewing safety data, and supporting trial operations. Success involves strong leadership, protocol ownership, team collaboration, and commitment to safety and data quality.
The role is PRN, onsite, with competitive pay and benefits, requiring English proficiency and availability Monday-Friday, with occasional on-call duties.
The role offers $5,000 sign-on bonus with 2.5 year commitment
Qualifications
- Texas-licensed physician
- Prior clinical research experience preferred (PI or Sub-Investigator)
- Ability to connect and deliver care to patients of all backgrounds
- Passion for relationship-driven, human-centered care
Responsibilities
- Your clinical experience will help drive the technology and care model innovations we build as we continue to enhance the patient experience and instill joy in the practice of medicine
- Your role as a Principal Investigator will help bring clinical trials as a care offering to patients, and grant other clinicians and staff oversight to engage in research
- Serve as a Principal Investigator for multiple clinical trials, Phases I to IV, where you will be responsible for the clinical research conduct and quality assurance, as well as supervising sub-investigators in their clinical trial work
- Attend site initiation visits, sponsor monitoring visits, and national conferences
- Evaluate a study volunteer's eligibility for clinical trials
- Be responsible for the successful execution of research protocols according to FDA regulations and GCP guidelines
- Review and provide guidance on labs, diagnostic reports, diary reports, safety reports, and AEs/SAEs within a trial