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ICON plc
Overview
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.
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Compensation
$91,336 - $114,170 / YEAR
Posted
2 days ago
Avalo Therapeutics
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
Salary not listed
6 days ago
Genmab
The MSL/Sr. MSL will develop and maintain relationships with medical thought leaders to support approved products and those in clinical development, providing scientific information through fair-balanced exchange. Responsibilities also include executing field medical activities, collaborating cross-functionally, and managing Investigator Sponsored Trials (ISTs).
$144,720 - $217,080 / YEAR
9 days ago
argenx
The MSL serves as a scientific expert engaging with Key Opinion Leaders to support medical strategy and identify unmet medical needs. They are responsible for identifying clinical trial sites, supporting research execution, and disseminating scientific data within the organization.
15 days ago
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
$110,520 - $138,150 / YEAR
16 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.
Pfizer
Conduct bifunctional immunological assays to support vaccine clinical development and maintain a detailed inventory of freezer reagents. Present progress on assay development and sample analysis, while executing sample testing and analysis for toxicology and clinical trials.
$60,200 - $100,400 / YEAR
The MSL is responsible for developing and enhancing professional relationships with medical thought leaders to support approved products and those in clinical development, providing scientific information through fair-balanced exchange. They will execute field medical activities, collaborate with cross-functional teams, and support new product launch excellence.
$162,320 - $243,480 / YEAR
The Medical Science Liaison (MSL/Sr. MSL) is responsible for developing and maintaining professional relationships with medical thought leaders to support approved products and those in clinical development. This includes providing scientific information, executing field medical activities, and supporting new product launch excellence through fair-balanced scientific exchange.
The Clinical Research Nurse provides direct clinical care to research participants and administers investigational products while monitoring safety. They also coordinate study procedures, ensure protocol compliance, and maintain accurate documentation of research data.
17 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.
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.
The Senior CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with site staff and contribute to the preparation of study documentation and clinical study reports.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
The Senior CRA oversees clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They conduct site visits, manage data collection, and provide training to site staff to ensure successful trial execution.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with site staff and investigators while performing data review to maintain high-quality clinical documentation.
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.
