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Johnson County Clintrials LLC
Overview
The Sub-Investigator provides medical oversight, evaluations, and care for volunteers participating in clinical research studies. They are responsible for screening participants, managing health toxicities, and ensuring strict adherence to study protocols and regulatory requirements.
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Compensation
Salary not listed
Posted
4 days ago
Evolution Research Group
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
10 days ago
IQVIA
The role involves performing physical exams, assessing lab values, and monitoring subject compliance and response to therapy. Additionally, the provider must document adverse events and communicate with primary care physicians and the research team.
$95,100 - $237,700 / YEAR
11 days ago
Hawthorne Health
Assist the Principal Investigator in managing clinical trials, ensuring adherence to protocols, GCP, and regulatory requirements. Provide medical oversight for study participants, including performing physical exams and interpreting diagnostic tests.
$100,000 - $150,000 / YEAR
DM CLINICAL RESEARCH GROUP
The Sub-Investigator is responsible for ensuring adherence to study protocols and protecting the rights and welfare of research subjects. They perform clinical safety assessments, manage medical care for subjects, and maintain data integrity according to federal and state regulations.
Be Well Clinical Studies
The Sub-Investigator supports the Principal Investigator in conducting clinical trials by performing medical procedures and ensuring protocol adherence. They are responsible for subject eligibility assessments, patient safety, and maintaining high standards of data integrity.
$65 - $90 / HOUR
12 days ago
SRI International
Perform Sub-Investigator duties including medical oversight, participant eligibility determination, and safety monitoring for clinical trials. Ensure all activities comply with study protocols, GCP guidelines, and regulatory requirements while collaborating with the Principal Investigator.
$43 - $61 / HOUR
Care Access
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.
$130,000 - $165,000 / YEAR
14 days ago
Greenlife Healthcare Staffing
Conduct on-site surveys and investigations at nursing homes to evaluate nutritional services and ensure regulatory compliance. Analyze findings to prepare detailed reports and assess the implementation of corrective action plans.
$39 / HOUR
16 days ago
17 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.
ObjectiveHealth
The Principal Investigator will serve as the lead for assigned clinical trials, ensuring overall study oversight and enforcing strict compliance with protocols while always prioritizing subject safety. This role involves conducting and documenting medical assessments and providing continuous medical oversight throughout the trial lifecycle.
29 days 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.
1 month ago
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.
Pinnacle Clinical Research
The Sub Investigator serves as a key team member responsible for conducting follow-up visits, reviewing labs, and recruiting subjects for study protocols. They perform clinical procedures and ensure strict adherence to FDA regulations and Good Clinical Practice (GCP) guidelines.
Assist the Principal Investigator in overseeing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all study-related data.
$150 / HOUR
Assist the Principal Investigator in managing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical trial data.
Conduct surveys and complaint investigations at nursing homes to ensure compliance with federal and state regulations. Produce written documentation, draft Statements of Deficiencies, and participate in state monitoring during immediate jeopardy situations.
$60 / HOUR
The IMA Group
The Principal Investigator will lead clinical trials, ensuring strict adherence to study protocols and regulatory requirements. They are responsible for evaluating participant eligibility, monitoring patient safety, and maintaining accurate study documentation.
Circuit Clinical
The Principal Investigator is responsible for the regulatory oversight, subject safety, and protocol compliance of industry-sponsored clinical research trials. They will perform study assessments, review adverse events, and provide medical supervision to research staff.
$120 - $150 / HOUR
