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Overview
The Sub-Investigator will oversee the execution of study protocols, ensuring site compliance with regulations, GCP, and SOPs, while delegating duties to site staff as appropriate. Responsibilities also include seeing subjects virtually or in-person, resolving medical issues, and administering investigational products via various routes.
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Compensation
$130,000 - $165,000 / YEAR
Posted
14 days ago
Civia Health
Conduct study visits including medical assessments and protocol-specific procedures. Partner with principal investigators to ensure quality, safety, and regulatory compliance.
Salary not listed
17 days ago
Fortrea
The Nurse Practitioner provides clinical expertise for Phase I trials, performing physical exams and participant assessments. They ensure adherence to GCP, FDA, and ICH regulations while serving as a technical advisor to clinical pharmacology teams.
23 days ago
Provide clinical expertise and serve as a sub-investigator to ensure participant safety and protocol adherence in Phase I clinical trials. Responsibilities include performing medical assessments, reviewing screening data, and ensuring compliance with FDA, GCP, and ICH regulations.
25 days ago
The Physician Assistant provides clinical expertise and support for Phase I clinical trials, including performing physical examinations and participant assessments. The role involves acting as a technical advisor to clinical teams and ensuring compliance with FDA, GCP, and ICH regulations.
1 month ago
Gastromed, LLC
The Sub-Investigator performs clinical assessments, ensures protocol adherence, and monitors subject safety throughout clinical trials. They collaborate with investigators and sponsors to maintain high-quality data and support patient recruitment efforts.
K2 Staffing LLC
The Sub Investigator ensures adherence to clinical trial protocols and federal regulations while protecting the rights and welfare of study subjects. They are responsible for managing the medical care of participants and maintaining the integrity of the data generated at the site.
Centricity Research
The Sub-Investigator supports the Principal Investigator in the oversight and conduct of clinical trials to ensure participant safety and protocol compliance. Responsibilities include performing physical exams, medical decision-making, obtaining informed consent, and mentoring site staff.
M3USA
The Sub-Investigator/Rater provides oversight in medical and clinical issues, working with the Principal Investigator to ensure all study procedures adhere to Good Clinical Practices (GCP). This role is primarily responsible for the accurate completion of visit procedures, collection of participant information per protocols, and protecting the health and safety of research participants.
$110,000 - $145,000 / YEAR
2 months ago
The Nurse Practitioner will conduct study visits, including medical assessments and physical exams, while partnering with principal investigators to ensure quality, safety, and regulatory compliance across clinical trials. Responsibilities also involve engaging participants empathetically, managing adverse events, and maintaining accurate documentation in source records and EDC systems.
Tandem Intermediate LLC
The Sub-Investigator provides direct medical care and oversight for patients within a clinical trial setting, including performing physical exams and administering investigational products. They collaborate with the Principal Investigator to ensure protocol compliance and accurate documentation of clinical data.
$120,000 - $135,000 / YEAR
3 months ago
The Sub Investigator is responsible for promoting Good Clinical Practice by ensuring adherence to protocol requirements, protecting study subjects' rights and welfare, and assuring data integrity at the site. This includes assuming responsibility for the conduct of the clinical investigation according to all federal and state regulations.
