Clinical Research PI (GCP/Regulatory)

Dm Clinical Research Group; Houston (TX); On-site; USD 180,000 - 240,000; Full time

Job summary

Paycom - ATS seeks a Clinical Research Investigator to oversee protocol conduct, protect subject welfare, and ensure data integrity at our Houston site. The role requires an MD or DO with an active license and at least two years of clinical research experience.

The investigator will ensure compliance with FDA, GCP/ICH, and SOPs, manage study documentation, and coordinate training and oversight of staff and procedures.

Qualifications

• Must hold MD or DO with active medical license valid in the state of the research.
• At least 2 years of experience as a Clinical Research Investigator.
• Knowledge of FDA regulations, GCP/ICH guidelines, SOPs and study protocols.

Responsibilities

• Complete DMCR-required training including GCP and IATA.
• Maintain knowledge of current FDA regulations, GCP/ICH guidelines, SOPs, and study protocols.
• Manage medical care of subjects and protect their rights and welfare.
• Ensure validity of trial data reported to sponsor and proper documentation of procedures.
• Facilitate patient consent discussions and ensure understanding of risks, benefits, and alternatives.
• Communicate effectively between patients, healthcare providers, and research staff.

Skills

Verbal and written communication

Bilingual English/Spanish

Education

MD or DO with active medical license

Job description

Paycom - ATS seeks a Clinical Research Investigator to oversee protocol conduct, protect subject welfare, and ensure data integrity at our Houston site. The role requires an MD or DO with an active license and at least two years of clinical research experience.

The investigator will ensure compliance with FDA, GCP/ICH, and SOPs, manage study documentation, and coordinate training and oversight of staff and procedures.