Ad Hoc Sub-Investigator – Remote Clinical Trial Role

About the role

SPRIM PRO is seeking qualified clinicians to join its urology clinical trial on an ad‑hoc, remote basis. This position is ideal for MDs or DOs who want to contribute to high‑impact research without a full‑time commitment, performing study visits and assessments that fit their schedule.

Key responsibilities

• Assess and confirm participant eligibility against protocol inclusion/exclusion criteria.
• Conduct protocol‑specified medical assessments, physical exams, and study visits.
• Evaluate, document, and manage adverse events, including causality and severity assessment.
• Review concomitant medications and prescribe investigational products as required.
• Maintain accurate, timely source documentation and ensure data integrity.
• Participate in site initiation, protocol training, and ongoing study updates.
• Ensure compliance with the approved protocol, GCP, regulatory, and IRB/EC requirements.

Required profile

• MD or DO with board certification and an active, unrestricted medical license (multistate preferred).
• Prior experience as an Investigator in industry‑sponsored clinical trials, with at least 3 years working with the study population.
• Current ICH‑GCP certification or willingness to obtain it before study start.
• Working knowledge of FDA 21 CFR, ICH E6, informed consent, and human subject protection.
• Flexible availability and reliable turnaround on assigned studies and visits.

Required skills

• ICH‑GCP certification
• Knowledge of FDA 21 CFR and ICH E6 regulations
• Familiarity with electronic data capture (EDC) systems
• Experience with clinical trial conduct and adverse event management