Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
University of Massachusetts Medical SchoolNew
Overview
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.
Quick view →
Compensation
Salary not listed
Posted
New
ICON plc
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$91,336 - $114,170 / YEAR
2 days ago
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
$110,520 - $138,150 / YEAR
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
University of Miami
The Research Associate 2 will conduct laboratory assignments, including preparing and preserving peripheral blood mononuclear cells (PBMC) and generating CAR T cells, while participating in scheduling and performing experiments related to immunology and leukocyte biology studies. This role involves conducting experimental procedures, maintaining accurate records, interpreting data, and providing technical support for various immunological and molecular biology assays.
3 days ago
Legend Biotech US
Perform preclinical in vivo pharmacology and toxicology studies using mouse, dog, and NHP models to support pipeline advancement. Responsibilities include cell culture, animal dosing, tumor measurement, and sample processing and analysis.
4 days ago
Keros Therapeutics
The role involves maintaining and culturing cell lines and conducting cellular assays to assess signaling events. The associate will also perform gene expression and protein detection analysis while collaborating on drug discovery projects.
$28 - $32 / HOUR
7 days ago
IQVIA
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
$71,900 - $169,300 / YEAR
9 days ago
St. Jude Children's Research Hospital
The Postdoctoral Research Associate will conduct research focusing on regulatory T cells in the context of autoimmune inflammation and anti-tumor immunity, designing and executing experiments using mouse models and human T cells. Responsibilities also include collaborating on data analysis and presenting findings in scientific journals and conferences.
$72,500 / YEAR
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
Altos Labs
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.
$109,200 - $140,000 / YEAR
10 days ago
The University of Alabama
Provides research support for the Healthy Brain and Child Development Study, including participant recruitment, retention, and guidance. Responsible for collecting data via MRI, EEGs, cognitive assessments, and bio-specimens while tracking community resource usage.
$21 - $27 / HOUR
AstraZeneca
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, and ensuring data quality through monitoring visits and source data review.
$112,154 - $168,232 / YEAR
11 days ago
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
Postdoctoral fellows will conduct research on childhood hematological malignancies, focusing on translating genomic discoveries into experimental models and therapeutic advances. They will participate in a multidisciplinary training program involving genomic analysis and preclinical modeling.
14 days ago
The Medical Research Associate is responsible for greeting clinical research volunteers and performing vital sign assessments and phlebotomy procedures according to study protocols. They also provide personalized care to study subjects and ensure their comfort throughout the research process.
16 days ago
The Medical Research Associate is responsible for greeting clinical research volunteers and performing vital sign assessments and phlebotomy procedures. They also ensure participant comfort and safety while strictly adhering to study protocols.
17 days ago
The Senior CRA will oversee clinical trial monitoring activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also conduct site visits, manage site performance, and collaborate with cross-functional teams to ensure accurate data collection.
The Senior Clinical Research Associate will conduct site qualification, monitoring, and close-out visits while ensuring protocol compliance and data integrity. They will also collaborate with investigators and contribute to the preparation of study documentation and clinical reports.
