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AstraZeneca
Overview
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.
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Compensation
$112,154 - $168,232 / YEAR
Posted
11 days ago
Science 37
Perform mobile clinical research nursing services and care delivery to study participants in their homes. Collaborate with the Nursing Solutions Group and brick-and-mortar sites to implement decentralized clinical trials in compliance with federal regulations.
$50 - $55 / HOUR
16 days ago
Perform mobile clinical research nursing services by visiting study participants in their homes to deliver care and conduct assessments. Collaborate with the Nursing Solutions Group and brick-and-mortar sites to implement decentralized clinical trial protocols.
Perform mobile clinical research nursing services by visiting study participants in their homes to deliver care and conduct assessments. Collaborate with the Nursing Solutions Group and brick-and-mortar sites to implement decentralized clinical trials in compliance with federal regulations.
Medpace, Inc.
The Clinical Data Review Associate will conduct comprehensive manual reviews of clinical data collected in trials and develop clinical review guidelines for specific therapeutic areas. They will also interface with the Data Management team to ensure query resolution.
Salary not listed
28 days ago
Syneos Health
Provide patient-focused clinical services including mobile research nursing and patient concierge for pharmaceutical and biotechnology industries. Support clinical trials across various phases and therapeutic areas to improve the patient experience.
$67,700 - $115,100 / YEAR
1 month ago
Hawthorne Health
Assist the Principal Investigator in managing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical trial data.
$150 / HOUR
Revival Research Institute, LLC
Coordinate and manage multiple clinical studies while assisting principal investigators with participant screening, recruitment, and enrollment. Maintain accurate study documentation, handle data queries, and ensure compliance with regulatory standards and quality control methods.
Nurse Practitioners will collaborate with a physician-led team and serve as subject experts on assigned projects. They will also develop clinical education materials and support study-related activities.
The Clinical Trial Assistant will provide day-to-day support for Training & Development activities, including maintenance of files and scheduling training sessions. Additional responsibilities include conducting quality control reviews and supporting other departments on ad hoc projects.
The TMF Document Administrator supports TMF oversight for a trial by ensuring documents meet established quality standards. This includes managing the electronic filing system for trial documentation and communicating with internal associates regarding errors in trial documents.
Fortrea
The Research Technician will interact with healthy volunteer participants to perform clinical procedures such as venipuncture, ECGs, and biological sample processing. They are also responsible for monitoring dietary compliance and maintaining a clean, safe, and efficient clinical study environment.
2 months ago
K2 Staffing LLC
The role involves performing IV insertions, administering investigational products, and monitoring patient safety during infusion therapy. Additionally, the nurse will assist the Principal Investigator and Clinical Research Coordinators with trial-related procedures such as lab collections and EKGs.
Key responsibilities include interacting directly with healthy volunteer participants, reading clinical research protocols, and accurately performing vital signs, ECGs, and biological sample collection and processing according to protocol specifications. The role also involves monitoring participant dietary compliance and assisting with room and equipment preparation in a fast-paced, team-oriented clinical environment.
Aquestive Therapeutics
The Medical Science Liaison supports therapeutic areas and approved products by engaging with healthcare community members to exchange scientific and clinical knowledge, focusing on educating stakeholders on safe and appropriate product use. This role also supports scientific knowledge generation and advances company projects using subject matter expertise.
$160,000 - $220,000 / YEAR
3 months ago
The Medical Science Liaison acts as a field-based medical expert to advance scientific and medical relationships by engaging with key healthcare community members, focusing on educating stakeholders on the science behind product use. This role supports the generation of scientific knowledge and applies expertise to advance company projects within a defined geographic territory.
The Medical Science Liaison acts as a field-based medical expert, engaging with healthcare community members to exchange scientific and clinical knowledge regarding AQST's therapeutic areas and approved products. This role involves educating stakeholders on safe and appropriate product use, supporting scientific knowledge generation, and advancing company projects.
Provide nursing coverage for the Medpace Clinical Pharmacology Unit according to study protocols and Good Clinical Practice. Perform clinical procedures and ensure accurate medication administration while documenting adverse events.
The Medical Science Liaison acts as a field-based medical expert to advance scientific and medical relationships by engaging with key healthcare community members, focusing on educating stakeholders on the science behind product use. This role supports scientific knowledge generation and applies expertise to advance company projects.
