Clinical Research PA Sub-Investigator

Revival Research Institute, LLC; McKinney (TX); On-site; USD 98,000 - 135,000; Full time

Job summary

Revival Research Institute, LLC is seeking a Physician Assistant (Associate) to serve as a Clinical Research Sub-Investigator, supporting safe, compliant conduct of trials under the Principal Investigator. The PA will ensure timely medical care and documentation per protocol, GCP, and sponsor requirements.

Responsibilities include clinical assessment, safety surveillance, data integrity, protocol discipline, and regulatory compliance across study sites.

Qualifications

• Graduate of an accredited Physician Assistant program; master's degree or higher preferred/required in accordance with licensure standards.
• Current, unrestricted Physician Assistant license in each state where duties are performed.
• Current NCCPA certification.
• Basic Life Support required; ACLS when applicable to study population/site.
• DEA registration and state controlled-substance authorization when required.
• At least two years of direct patient-care experience preferred; clinical research experience preferred.

Responsibilities

• Clinical assessment and protocol execution within delegated authority.
• Participant safety surveillance and escalation of safety concerns.
• Source documentation and data integrity; accurate medical records.
• Protocol discipline and adherence to approved materials.
• Regulatory compliance including informed consent, safety reporting, and essential documentation.
• Operational reliability: manage visits, signatures, queries, and follow-ups.
• Cross-functional coordination with clinical, regulatory, pharmacy, laboratory, recruitment, quality, and sponsor teams.

Skills

Communication

Attention to detail

Safety awareness

Education

PA program graduate

Tools

EMR systems

CTMS

eSource

Job description

Revival Research Institute, LLC is seeking a Physician Assistant (Associate) to serve as a Clinical Research Sub-Investigator, supporting safe, compliant conduct of trials under the Principal Investigator. The PA will ensure timely medical care and documentation per protocol, GCP, and sponsor requirements.

Responsibilities include clinical assessment, safety surveillance, data integrity, protocol discipline, and regulatory compliance across study sites.