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Headlands Research
Overview
The Nurse Practitioner or Physician Assistant will serve as a Sub-Investigator, ensuring the safety and welfare of clinical trial subjects. Responsibilities include conducting medical history interviews, performing physical examinations, and reviewing lab results according to research protocols.
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Compensation
Salary not listed
Posted
6 days ago
Lead and oversee clinical trials, ensuring compliance with protocol requirements and regulatory standards. Provide leadership and mentorship to site staff while fostering a culture of inclusivity and professionalism.
Evolution Research Group
The Sub-Investigator acts as the secondary physician overseeing clinical trials, ensuring protocol adherence and regulatory compliance at the research site. They are responsible for managing subject care, documenting study procedures, and maintaining the integrity of clinical data.
$100,000 - $150,000 / YEAR
9 days ago
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.
The Sub-Investigator will ensure the safety and welfare of study subjects by maintaining in-depth knowledge of all research protocols, screening subjects, conducting medical interviews and exams, reviewing results, and providing necessary medical care during trials. Responsibilities also include providing home-based on-call availability and attending Investigator Meetings when required.
Lead and oversee clinical trials ensuring compliance with protocols and ethical guidelines. Provide leadership and mentorship to site staff while overseeing subject safety and trial conduct compliance.
$130 - $160 / 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
13 days ago
Nira Medical
Provide specialized care for patients with movement disorders, including Parkinson's disease and dystonia, within an outpatient setting. Manage advanced therapeutics such as DBS programming and botulinum toxin injections while participating in clinical research trials.
25 days ago
Alcanza Clinical Research
Acts as a Sub-Investigator to perform medical assessments, manage subject safety, and implement IRB-approved protocols. May also function as a Clinical Research Coordinator to manage daily research activities and regulatory documentation.
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.
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.
Hawthorne Health
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.
$150 / HOUR
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.
Assist the Principal Investigator in managing clinical trials, ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical data.
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
Civia Health
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.
Sansum Diabetes Research Institute
The Nurse Practitioner will serve as a Sub-Investigator, leading the clinical research team in medical aspects of trials under the Principal Investigator's supervision. Key duties include performing clinical research activities, ensuring protocol compliance, administering investigational medications, and providing direct care to study patients.
$70 - $100 / HOUR
3 months ago
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
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.
