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Summit Therapeutics
Overview
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.
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Compensation
$200,000 - $235,000 / YEAR
Posted
3 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
9 days ago
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
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.
Salary not listed
15 days ago
M3USA
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.
$30 - $40 / HOUR
16 days ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
Chiesi Group
The MSL is responsible for building partnerships with Key Opinion Leaders (KOLs) and healthcare professionals to exchange scientific data and provide medical education. They support clinical development, gather field insights, and represent the company at scientific meetings within the Central US territory.
$165,000 - $190,000 / YEAR
20 days ago
PsychoGenics Inc.
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.
29 days ago
Kamada
The MSL will build trusted relationships with Key Opinion Leaders and healthcare professionals to provide scientific education and identify clinical opportunities. They will also collaborate on data generation initiatives and relay medical insights to internal stakeholders to inform company strategy.
1 month ago
Pharmaron
Support preclinical translational research in ophthalmology by performing in vivo procedures, dosing, and imaging on rodent and rabbit models. Ensure study compliance with GLP regulations and maintain accurate data entry within internal systems.
$25 - $35 / HOUR
Perform clinical procedures including phlebotomy, ECGs, and specimen collection while ensuring strict protocol adherence. Support daily study operations, real-time data entry, and provide high-quality care to research participants.
$20 - $23 / HOUR
Vedanta Biosciences
The Senior Clinical Trial Associate serves as a central hub for the clinical study team, supporting the planning, implementation, and wind-down of clinical trials. Key duties include managing the Trial Master File, coordinating with CROs, and tracking study status and enrollment.
$48 - $55 / HOUR
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.
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, and ensuring all activities comply with the research protocol and regulations.
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 and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening study participants, maintaining documentation, and ensuring compliance with research protocols.
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with screening, maintaining documentation, collecting and entering data, and mentoring junior staff.
PharmaEssentia U.S.A.
The Medical Science Liaison will facilitate the exchange of medical information with healthcare professionals regarding myeloproliferative neoplasms. They are responsible for building relationships with key opinion leaders and providing scientific support for clinical trials and medical education.
$170,000 - $230,000 / YEAR
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
