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Altos Labs
Overview
Execute research and development experiments using human iPSC models to support cellular rejuvenation and aging studies. Develop innovative laboratory techniques and provide technical mentorship and training for specialized in vitro culture workflows.
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Compensation
$109,200 - $140,000 / YEAR
Posted
10 days ago
American Addiction Centers
Conduct and manage funded neuroscience research projects focusing on neurological function and disease using mouse models and cell culture. Responsibilities include designing experiments, analyzing complex data, preparing manuscripts, and mentoring laboratory personnel.
$31 - $46 / HOUR
Rapport Therapeutics
The Senior Clinical Trial Associate manages clinical study documentation, including the Trial Master File, to ensure inspection readiness and compliance with ICH-GCP standards. They also support the trial team with administrative tasks, vendor invoice tracking, and the preparation of essential study-related documents.
$90,000 - $110,000 / YEAR
The Research Fellow will implement community-based human subjects research studies and manage the collection and analysis of quantitative and qualitative data. They will also engage with community partners and produce high-quality scholarly writing, including manuscripts and grant applications.
17 days ago
Quotient Sciences
The primary duties involve collecting biological samples, performing phlebotomy, recording vital signs, and ensuring all study data collection adheres to Good Clinical Practice (GCP) standards for participant safety.
Salary not listed
21 days ago
Oruka Therapeutics
The Administrative Assistant will manage complex calendars, coordinate travel, and handle expense reporting for multiple team members. They will also oversee office logistics, including meeting support, kitchen inventory, and vendor coordination.
$28 - $35 / HOUR
27 days ago
Castle Biosciences
Responsible for triaging, sorting, and accessioning clinical specimens into the laboratory information system. Ensures accurate data entry and compliance with company policies and quality standards.
28 days ago
The Molecular Technologist performs multiplexed immunofluorescent labeling, digital imaging, and quality control reviews for clinical tests. Responsibilities also include specimen management, reagent preparation, and maintaining documentation for high-complexity laboratory testing.
29 days ago
Sanofi
The MSL provides non-promotional scientific and educational support for Dupilumab in the asthma therapeutic area. They are responsible for building relationships with key respiratory experts and acting as a conduit for medical information between the company and healthcare professionals.
$146,250 - $211,250 / YEAR
1 month ago
Thermo Fisher Scientific
The technician is responsible for collecting and harvesting laboratory specimens such as plasma and serum according to protocol. They also monitor urine and fecal specimens while ensuring processing areas remain clean and organized.
The Clinical Research Nurse conducts clinical trials by providing medical care to patients and ensuring adherence to FDA, GCP, and ICH regulations. Responsibilities include performing protocol procedures, managing patient documentation, and coordinating with site teams from study initiation to closeout.
GRAIL
The Clinical Project Assistant supports study teams in Clinical Operations by managing administrative aspects of clinical trial execution. Key duties include maintaining the Trial Master File, tracking site payments, and assisting with quality metrics and meeting coordination.
$33 - $39 / HOUR
Alnylam Pharmaceuticals
Design and execute in vivo pharmacology studies in autoimmune and tumor models to support therapeutic development. Perform ex vivo analyses and collaborate with internal teams and external CROs to advance drug discovery programs.
$110,400 - $165,600 / YEAR
FULGENT THERAPEUTICS LLC
The Specimen Processing Specialist is responsible for verifying patient and physician data and accurately entering information into the laboratory information system. They must also identify and resolve issues with specimen types or missing information while maintaining productivity and quality standards.
The Imaging Specialist performs quality control functions on pathology cases and captures digital microphotographs for final reports. They are responsible for maintaining accurate documentation, prioritizing cases, and ensuring laboratory safety and quality standards are met.
Immune Biopharma
The administrative assistant will manage inbound communications, coordinate scheduling, and maintain office files and supplies. They will also act as a point of contact for visitors and facilitate executive-level operations such as travel booking and expense reporting.
$41,850 - $54,330 / YEAR
The Grossing Technician II assists pathologists by performing accurate gross descriptions and dissections of surgical specimens. They are responsible for maintaining laboratory documentation, ensuring regulatory compliance, and managing specimen triage and chemical waste.
The Molecular Technologist is responsible for extracting and analyzing RNA samples using various molecular techniques including PCR and quantification. They must also ensure data accuracy, maintain laboratory instruments, and collaborate with team members to optimize workflow.
Medpace, Inc.
The role involves engaging in day-to-day clinical trial management, working closely with the CTM to ensure timely and accurate task delivery. Responsibilities also include compiling status reports, interacting with various stakeholders, and managing internal regulatory filing oversight and study supplies.
