Clinical Research Jobs in the United States
Axelon Services Corporation
Los Angeles, CA
AMIA Health Informatics Certification (AHIC): Certified Health Data Analyst (CHDA): Certified in Healthcare Privacy and Security (CHPS): Registered Health Information Administrator (RHIA): Certified Professional in Healthcare Information and Management Systems (CPHIMS): Certified associate in healthcare information and management systems (CAHIMS): **Must Have's:**. Responsibilities include acting as a liaison between clinicians/researchers and data stewards, interfacing with stakeholders on informatics software development, maintenance, and operations, and creating streamlined workflows for the exploitation of healthcare data.
Axelon Services Corporation
New York, NY
Flexibility 2. Excellent written and verbal communication 2. Organized 3. Technology: outlook, Excel, Microsoft 3. Education Requirement: AS Education Preferred: BSN Software Skills Required: Word, Outlook, Excel, Microsoft, Adobe, EMS Required Certifications: RN, NY State Driver s License Required Testing: UAS Each day varies, nurse needs to be flexible with schedule and process changes, critical thinking and problem solving, prepared for travel, weather variability.
Axelon Services Corporation
New York, NY
Flexibility 2. Excellent written and verbal communication 2. Organized 3. Technology: outlook, Excel, Microsoft 3. Education Requirement: AS Education Preferred: BSN Software Skills Required: Word, Outlook, Excel, Microsoft, Adobe, EMS Required Certifications: RN, NY State Driver s License Required Testing: UAS Each day varies, nurse needs to be flexible with schedule and process changes, critical thinking and problem solving, prepared for travel, weather variability.
Axelon Services Corporation
Cambridge, MA
Experience in experimental design, data analysis, troubleshooting, and a range of biology skill sets including in vitro cell assay development, plate-based assays, Western blotting, protein quantification, ELISA, MSD, transfections, lentiviral transductions, siRNA/shRNA/CRISPR, qPCR, and viability assays. The ideal candidate will contribute to our discovery pipeline from the bench by taking responsibility for developing, optimizing, and troubleshooting cellular assays to characterize and advance Client molecules of interest.
Axelon Services Corporation
Cambridge, MA
Experience in experimental design, data analysis, troubleshooting, and a range of biology skill sets including in vitro cell assay development, plate-based assays, Western blotting, protein quantification, ELISA, MSD, transfections, lentiviral transductions, siRNA/shRNA/CRISPR, qPCR, and viability assays. The ideal candidate will contribute to our discovery pipeline from the bench by taking responsibility for developing, optimizing, and troubleshooting cellular assays to characterize and advance Client molecules of interest.
Axelon Services Corporation
Seattle, WA
Responsible for developing potency assays for both early- and late-stage development programs, as well as creating fit-for-purpose biological characterization assays. The Potency Group is seeking a Scientist within the Cell Therapy Analytical Development Organization to lead potency assay development and functional characterization for cell therapy products.
Axelon Services Corporation
Los Angeles, CA
Experimental Frameworks and Healthcare Analytics: While candidates have implemented advanced AI/ML systems, they haven't highlighted their experience in creating experimental frameworks for data collection or healthcare-specific analytics. The incumbent will work closely with Client researcher teams to design analysis specifications, including input data specifications, data cleaning, algorithms, and interpretation of results.
Axelon Services Corporation
Coventry, RI
Education:Bachelor's Degree from an accredited institution in Engineering, Engineering Technology or relevant/related disciplines. Work directly on 3D composites processing equipment and provide hands on support to manufacturing and process engineers.
Axelon Services Corporation
New York, NY
Organize and oversee inventory by keeping a detailed database of available inventory and expected usage per project; Train and instruct other members of the Supply Chain team; Plan and implement supply chain optimization projects; Seek to improve all aspects of the supply chain department by reviewing current methodology and processes; Research and seek out the most cost-efficient shipment procedures and methods; Maintain a friendly and professional relationship with vendors while promoting company initiatives and values; Research partner companies and seek to negotiate best-price contracts to increase business revenue; Work closely with the IT department to create effective databases to manage and organize warehouse inventory. As a supply chain manager, you'll oversee and manage every stage of the production flow, from purchasing the raw materials to the delivery of the final product.
Joulé
Piscataway, NJ
D.", "PhD", "Doctorate", "cell biology", "virology", "protein engineering", "antibody research", "antibody engineering", "protein engineering", "DNA cloning", "protein production", "protein purification", "cell-based assays", "FACS", "transfection", "RNA analysis", "protein analysis", "immunostaining", "viral transduction", "in vitro", "viral transduction assays", "ELISA", "Western blotting", "qPCR", "mammalian expression systems", "protein purification" As a key member of the team, you will play a crucial role in the design, production, and evaluation of bi-specific and multi-specific antibodies, as well as participate in a variety of cell and molecular biology techniques.
Joulé
Princeton, NJ
This position offers invaluable hands-on experience in a dynamic and innovative environment, providing a unique chance to contribute to cutting-edge projects while gaining professional exposure in the field of toxicology. A leading consumer products company based in Central New Jersey is seeking a talented Toxicology student to join their team for an exceptional summer opportunity.
Joulé
Carnegie, PA
Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes. A top-ranked research university is currently searching for a Clinical Research Coordinator for one of its growing departments to be responsible for assisting in the operations of ongoing clinical trials.
Joulé
Asheville, NC
Duties and Responsibilities: Duties include but are not limited to: • Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements . • Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications .
Joulé
Nashville, TN
Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications . Duties and Responsibilities: Duties include but are not limited to: • Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements .
Joulé
Rochester, NY
Key Responsibilities: Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study related supplies and equipment, assisting with monitoring visits, attending Investigator Meetings, and assisting with query resolution, as required. Facilitate ongoing Quality Assurance (QA) review of studies, in collaboration with the QA department, including assisting with risk assessments, root cause analysis, and development of corrective and preventative actions as applicable.
Joulé
Pittsburgh, PA
This role demands expertise in financial management within a clinical trials setting, a strong background in research accounting, and a keen understanding of compliance and auditing. Our client, a newly formed department at a prestigious research university, is seeking a Senior Post Award Analyst.
Joulé
Carnegie, PA
A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process. Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.
Joulé
$32 - $40 undefined
Pittsburgh, PA
The Office of Clinical Trials (OCT) at our client is seeking a Clinical Research Support Specialist with experience in clinical research. Work with study teams and/or sponsors to gather required documents to facilitate central office review process.