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Orlando HealthNew
Overview
Develop and implement administrative strategies to manage clinical trials and coordinate large-scale research studies. Responsibilities include assessing patient eligibility, monitoring adverse reactions, and ensuring adherence to FDA and protocol guidelines.
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Compensation
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Posted
New
UTHealth HoustonNew
Assists with the conduct and management of human subject research projects, including participant recruitment and data collection. Responsible for maintaining databases, preparing progress reports, and supporting grant proposals and regulatory submissions.
The Ohio State UniversityNew
Provide support for clinical research studies within the Division of Cardiovascular Medicine, including study implementation and coordination. Responsibilities include recruiting participants, performing diagnostic testing, and managing clinical research data.
Medical University of South CarolinaNew
The incumbent will coordinate the recruitment, screening, and enrollment of research participants while collecting psychological and biological data. They are also responsible for maintaining regulatory documentation and providing administrative support for grant proposals and publications.
$37,200 - $59,500 / YEAR
Mass General BrighamNew
Coordinate and run study visits involving neuroimaging and biological sample collection for infection-associated health conditions. Manage IRB compliance documents, screen potential participants, and assist with data processing and analysis.
$21 - $29 / HOUR
UVA HealthNew
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
$28 - $81,500 / HOUR
1000 Wellstar Health System, Inc.New
The role involves owning the nursing process from assessment through evaluation to deliver personalized, evidence-based care while building meaningful connections with patients and families. Responsibilities also include fostering a safe, respectful team environment and actively participating in performance improvement projects and shared governance.
The coordinator will recruit, screen, consent, and enroll participants across multiple cancer clinical trials while building relationships with study participants. Key duties include coordinating study visits, collecting high-quality data, maintaining accurate documentation, processing specimens, tracking adverse events, and ensuring protocol compliance.
$28 - $82 / HOUR
Children’s Hospital of PhiladelphiaNew
The physician evaluates and treats patients in applicable medical or surgical specialties within various care settings, documenting findings in EPIC and collaborating with clinical and administrative staff. Responsibilities include providing direct patient care, supervising clinical providers, performing therapeutic interventions to stabilize acute problems, and managing the plan of care based on patient response.
$36,279 - $678,760 / YEAR
BHSNew
The Physical Therapist will evaluate and treat patients, develop individualized treatment plans, and educate patients and families. Additional responsibilities include supervising departmental personnel and communicating with healthcare providers regarding patient care.
As a Med Surg RN, you will deliver personalized, evidence-based care while building meaningful connections with patients and families. You will also contribute to performance improvement projects and support continuous improvement through data and research initiatives.
The RN Medsurg will own the nursing process from assessment through evaluation, delivering personalized, evidence-based care while building meaningful connections with patients and families. They will also contribute to teamwork, engage in performance improvement projects, and support continuous improvement initiatives.
Syneos HealthNew
The Medical Assistant will ensure the safety and well-being of study participants while performing clinical tasks and supporting clinical trials. They will also guide participants through the informed consent process and manage study supplies.
$35,600 - $60,400 / YEAR
Arizona Liver HealthNew
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
$28 - $36 / HOUR
University of Massachusetts Medical SchoolNew
The Research Associate I provides operational support to the laboratory by performing experiments and maintaining accurate research records. They are responsible for interpreting data, monitoring supply levels, and ensuring compliance with safety and institutional protocols.
UT Southwestern Medical CenterNew
The role involves performing technical research on genetic programs in the brain and analyzing mouse models of autism using molecular and genomic approaches. Additionally, the assistant is responsible for mouse colony management and general laboratory maintenance.
UT Health San Antonio
The research assistant will coordinate and participate in clinical research activities including participant recruitment, consenting, and cognitive assessments. They will also perform administrative duties, data entry, and quality control reviews while working closely with investigators.
2 days ago
UT Southwestern Medical Center
Provide technical assistance for preclinical research studies evaluating gene therapy in rodent models of neurological disorders. Responsibilities include conducting behavioral assays, monitoring animal health, and maintaining research rodent colonies.
The role involves performing technical research on genetic programs in the brain using molecular, biochemical, and genomic approaches. Responsibilities also include managing mouse colonies, general lab maintenance, and collaborating on scientific papers.
