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IQVIA
Overview
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.
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Compensation
$71,900 - $169,300 / YEAR
Posted
9 days ago
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
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
11 days ago
Olema Oncology
Provide administrative and operational support to clinical teams for in-house and outsourced trials. Manage study documentation, vendor relationships, and investigator site communications to ensure trial execution.
$110,000 - $120,000 / YEAR
27 days ago
Best Care
Coordinates clinical research studies including regulatory compliance, study start-up, subject follow-up, and record maintenance. Manages trial oversight, participant safety, and the handling of investigational products.
Salary not listed
28 days ago
QIAGEN
The CRA acts as the primary contact for clinical study sites, managing start-up, monitoring, and high-quality data collection. They ensure research is conducted according to regulatory standards while protecting the rights and safety of human subjects.
$65,000 - $75,000 / YEAR
1 month ago
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
ZOLL Medical Corporation
Provide administrative and operational support for clinical trials, including the maintenance of trial master files and regulatory documentation. Coordinate study activities, manage clinical data in CTMS and EDC systems, and ensure compliance with GCP and SOPs.
$28 - $32 / HOUR
Pharmaron
The Clinical Regulatory Associate manages essential clinical trial documentation, IRB submissions, and study start-up activities. They ensure compliance with GCP, GLP, and internal procedures while supporting monitoring visits and study closeout activities.
$50,000 - $54,000 / YEAR
Perform site monitoring and management to ensure study compliance with protocols, regulations, and sponsor requirements. Manage study progress, including regulatory submissions, recruitment tracking, and data integrity verification.
$64,000 - $189,000 / YEAR
Johnson & Johnson Innovative Medicine
The Clinical Trials Assistant supports the clinical study team with project communications, site payments, and file management. They are responsible for maintaining clinical databases, processing regulatory documents, and ensuring study supplies are managed effectively.
$41,000 - $66,700 / YEAR
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The Clinical Research Associate is responsible for performing site monitoring visits to ensure study protocol adherence and regulatory compliance. They also manage site recruitment plans, maintain study documentation, and oversee data integrity throughout the clinical trial process.
$87,200 - $182,000 / YEAR
Caris Life Sciences
The Clinical Trial Specialist provides operational and regulatory support for sponsored and collaborative studies, including site onboarding and IRB submission management. They are also responsible for maintaining study documentation, tracking clinical biospecimens, and ensuring compliance with Good Clinical Practice guidelines.
The Senior CRA is responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. They conduct site visits, support subject recruitment, and maintain essential study documentation to ensure data integrity.
$87,200 - $169,300 / YEAR
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
PTC Therapeutics, Inc.
The Contract, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations, assisting Clinical Trial Managers with various activities. Responsibilities include managing clinical documents, ensuring compliance with regulatory requirements, and supporting budget management.
$35 - $47 / HOUR
The Contract, Clinical Trial Associate provides support for clinical study and Trial Master File (TMF) activities, assisting Clinical Trial Managers with study start-up and document management. Responsibilities also include ensuring compliance with regulatory requirements and managing vendor invoices.
Medpace, Inc.
The Clinical Records Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This role involves managing electronic filing systems, tracking documents, and communicating with internal associates globally.
