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Evolution Research Group
Overview
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.
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Compensation
$100,000 - $150,000 / YEAR
Posted
9 days ago
Yale New Haven Health
The pharmacy intern provides operational support in the processing, production, inventory, and distribution of pharmaceuticals. They also participate in clinical and administrative functions under the supervision of a licensed pharmacist to gain practical experience.
Salary not listed
1 month ago
Lurie Children's Hospital
The role supports clinical and behavioral health research projects by assisting with study implementation, regulatory documentation, and IRB submissions. Responsibilities also include participant recruitment, data collection via REDCap, specimen processing, and maintaining study-specific records.
$46,280 - $75,670 / YEAR
The Behavioral Research Coordinator II manages research projects, including study start-up, protocol coordination, and regulatory documentation. They also conduct research visits, facilitate behavioral interventions, and perform data abstraction and quality assurance checks.
$49,920 - $81,619 / YEAR
University of Colorado
This position manages clinical trial treatment plans and ensures adherence to FDA, NCI, and institutional regulatory standards. The role involves collaborating with research teams to document clinical procedures and performing informatics support to improve research workflows.
$40,762 - $51,849 / YEAR
This position is responsible for conducting key aspects of Phase I-IV clinical trials in accordance with FDA regulations and institutional standards. The role involves managing treatment plans, performing clinical research informatics, and collaborating with multidisciplinary teams to ensure effective study documentation.
HonorHealth
The coordinator facilitates regulatory affairs for clinical research, ensuring compliance with FDA, ICH, and IRB standards. They manage study protocols from startup through closure, including document preparation and regulatory correspondence.
Dyne Therapeutics
The Principal Scientist will lead the strategic planning and execution of nonclinical safety programs for antibody and oligonucleotide therapeutics. They will manage external CRO relationships, interpret toxicology data, and author regulatory submissions to support clinical development.
$159,000 - $195,000 / YEAR
Flourish Research
The Regulatory Specialist manages and coordinates all regulatory documents and activities for clinical research studies. This includes overseeing submissions to IRBs and sponsors while ensuring compliance with federal regulations and site protocols.
$24 - $29 / HOUR
Taiho Oncology, Inc.
The incumbent manages global regulatory affairs dossier publishing activities, including document preparation and review for various health authority submissions. They also contribute to the development of publishing processes and ensure all dossiers meet regulatory and ICH standards.
$86,700 - $102,000 / YEAR
2 months ago
The incumbent supports global regulatory affairs dossier publishing activities, including document preparation, review, and submission tracking. They collaborate with subject matter experts to ensure all dossiers meet health authority and ICH standards for submissions like IND, NDA, and MAA.
The Regulatory Affairs Coordinator independently manages all IRB and regulatory processes for ophthalmology research studies. Responsibilities include preparing regulatory submissions, maintaining investigator site files, and ensuring compliance with institutional and federal regulations.
$59,995 - $87,761 / YEAR
UCSF
The Clinical Research Coordinator will manage and coordinate research protocols, including patient recruitment, consent, and data collection. They will also oversee data integrity, maintain regulatory documents, and assist with staff training and protocol compliance.
$38 / HOUR
RCCA MSO LLC
The Research Coordinator serves as the primary point of contact for clinical trials, overseeing study procedures from start to finish. Responsibilities include patient recruitment, data management, regulatory documentation, and ensuring compliance with safety protocols and institutional guidelines.
$27 - $37 / HOUR
3 months ago
The Regulatory Coordinator Assistant is responsible for preparing, compiling, and submitting regulatory documents for clinical trials while ensuring compliance with FDA and IRB regulations. They also manage site documentation, coordinate monitoring visits, and address inquiries from sponsors and clinical trial teams.
