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PsychoGenics Inc.New
Overview
The candidate will support preclinical studies using rodent models by performing dosing, surgical nursing, and behavioral assessments. They are also responsible for tissue collection, data handling, and coordinating study execution.
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Compensation
Salary not listed
Posted
New
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.
2 days ago
Neurocrine Biosciences
Oversee bioanalytical method development, validation, and sample analysis at contract research organizations (CROs) for small and large molecules. Coordinate with Clinical Pharmacology and Operations to ensure regulatory compliance and timely delivery of study data.
$53 - $77 / HOUR
4 days ago
Summit Therapeutics
The Senior MSL serves as a field-based scientific expert providing strategic support for oncology therapeutic areas and communicating science to healthcare professionals. Key duties include executing territory plans, supporting clinical research initiatives, and maintaining relationships with external experts in Immuno-Oncology.
$200,000 - $235,000 / YEAR
5 days ago
UCB
The MSL provides peer-level scientific exchange with clinicians and researchers to support optimized patient care in neuromuscular diseases. They are responsible for managing stakeholder relationships, generating medical insights, and supporting research collaborations.
$134,000 - $176,000 / YEAR
Assembly Biosciences, Inc.
Execute in vitro experiments to identify and characterize small molecules that inhibit viral infection. Optimize cell-based or biochemical assays and manage compound inventories and experimental data.
$87,000 - $91,300 / YEAR
8 days ago
Entrada Therapeutics
Support day-to-day operations of assigned clinical trials from start-up to close-out in compliance with ICH/GCP guidelines. Manage trial documentation, vendor payments, and clinical trial supplies while providing regular progress updates to the team.
9 days ago
Gilead Sciences
Supports the lifecycle of regulatory documents from creation to completion, ensuring adherence to eCTD specifications and standards. Collaborates cross-functionally with Research, Regulatory Affairs, and Clinical Development to ensure timely availability of submissions.
$117,895 - $152,570 / YEAR
10 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
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
$70,000 - $95,000 / YEAR
Alkermes
The intern will assist with drug discovery, target validation, and assay development using in vitro neuronal cultures. Responsibilities include routine cell culture maintenance, data management, and preparing scientific presentations.
$23 - $27 / HOUR
11 days ago
AstraZeneca
Perform animal husbandry duties including housing, feeding, and sanitation while maintaining high standards of animal welfare. Plan and document in vivo techniques to support preclinical research studies and communicate findings to stakeholders.
$52,245 - $78,367 / YEAR
12 days ago
Supports operational activities for the planning, initiation, conduct, and close-out of domestic and global clinical studies. Manages essential document collection, IRB/IEC submissions, and ensures compliance with GCP and regulatory standards.
$89,800 - $123,000 / YEAR
15 days ago
Javara
Support clinical studies by assisting with data entry, participant recruitment, and screening based on study criteria. Provide in-clinic support including shadowing study visits, processing lab specimens, and preparing research documentation.
16 days ago
Immatics
The MSL will facilitate high-quality scientific exchange and clinical research support with thought leaders and medical centers. They will support pre-launch and launch initiatives for TCR T-cell therapies in melanoma and other solid tumor indications.
$200,000 - $230,000 / YEAR
M3USA
The Clinical Research Assistant supports daily clinical trial activities, ensuring protocol compliance and data quality under the guidance of site leadership. Key duties include managing clinical supplies, performing phlebotomy, and documenting participant data in source records and EDC systems.
18 days ago
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
$30 - $40 / HOUR
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
