Part-Time Sub-Investigator, Psychiatry CNS Trials

Empathx Clinical Research

Dallas (TX)

Vor Ort

USD 83.000 - 138.000

Teilzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Empathx Clinical Research is seeking a Part-Time Sub-Investigator to provide medical oversight for psychiatric/CNS trials across Phases I–IV at our Dallas site. This on-site role requires reviewing eligibility, performing protocol-required assessments, and ensuring regulatory compliance with ICH-GCP and FDA rules.

The position supports 3–4 days per week (20–24 hours) with scheduling coordinated with the site. Licensure in Texas and experience in clinical research are essential.

Qualifikationen

  • Current and unrestricted licensure in the State of Texas (MD/DO/NP/PA‑C).
  • Master's Degree or equivalent in a related field or equivalent experience.
  • Experience as Sub Investigator or Clinical Research Coordinator preferred.

Aufgaben

  • Provide medical oversight for psychiatric/CNS trials across Phases I–IV.
  • Assess participant eligibility and safety per protocol and regulatory requirements.
  • Conduct informed consent processes and document in case report forms.
  • Evaluate AEs/SAEs and communicate safety concerns to the PI.
  • Collaborate with study staff to ensure protocol compliance and data integrity.

Kenntnisse

Clinical Trial Oversight
Psychiatry/CNS
EDC familiarity
Team leadership
Bilingual Spanish preferred

Ausbildung

Master's Degree or equivalent
MD/DO/NP/PA‑C license (TX)

Tools

EDC systems (Medidata Rave, REDCap)
CTMS/eRegulatory/eTMF
EMR/EHR

Jobbeschreibung

Empathx Clinical Research is seeking a Part-Time Sub-Investigator to provide medical oversight for psychiatric/CNS trials across Phases I–IV at our Dallas site. This on-site role requires reviewing eligibility, performing protocol-required assessments, and ensuring regulatory compliance with ICH-GCP and FDA rules.

The position supports 3–4 days per week (20–24 hours) with scheduling coordinated with the site. Licensure in Texas and experience in clinical research are essential.

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