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United Urology Group
Overview
The Research Coordinator will screen, enroll, and follow study subjects for clinical trials, ensuring protocol compliance and monitoring. Responsibilities include conducting clinical trials, enrolling subjects, and managing follow-up procedures.
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Compensation
$27 - $31 / HOUR
Posted
24 days ago
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
1 month ago
CenExel
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and performing data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
2 months ago
HUCKEYE HEALTH SERVICES LLC
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$48 / HOUR
The role involves maintaining full knowledge of laboratory procedures, assisting the manager with site preparation, and managing laboratory documentation like harvest logs and sample manifests. Responsibilities also include obtaining, processing, and properly storing study samples according to protocol and ensuring freezer/refrigerator temperatures are maintained.
$20 - $21 / HOUR
The role involves executing laboratory procedures according to protocol, assisting the laboratory manager with site preparation, and maintaining detailed logs for sample handling and inventory. Responsibilities also include obtaining, processing, and properly storing biological samples while ensuring equipment and storage temperatures are maintained.
The role is responsible for assisting in coordinating clinical trials while strictly adhering to ICH, GCP, protocol, and company guidelines, managing all aspects of patient involvement from initiation to completion. Duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments as required.
$30 - $33 / HOUR
The role is responsible for administering various clinical and neurocognitive test evaluations and interviews/ratings on study participants according to the protocol, including assessing cognitive, neuropsychological, behavioral, and functional status. Essential duties involve conducting clinical rating scales to confirm diagnoses, assisting the Principal Investigator (PI) in maintaining data integrity, and ensuring continuity of data collection among rating staff.
Salary not listed
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various study documents for trends, and performing ongoing quality reviews of study records and documentation.
Tribe513 | The Onyx Group
The Clinical Research Coordinator is primarily responsible for conducting Phase II, III, and IV clinical trials according to international standards, overseeing assigned trials under the direction of the Primary Investigator and Site Lead. Key duties include managing the informed consent process, medical record review, protocol compliance, patient relations, and administration of investigational products.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for all Case Report Forms (CRFs).
$20 - $23 / HOUR
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to all relevant guidelines and policies. Key duties involve creating and maintaining patient charts, managing study supplies, timely data entry and query resolution, and assisting with participant assessments and scheduling.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
This role involves performing select diagnostic testing across laboratory disciplines like hematology, urinalysis, and chemistry, requiring minimal interpretation. Essential duties include maintaining laboratory logs, monitoring sample storage temperatures, preparing supplies, and ensuring strict adherence to clinical research regulations and SOPs.
The Research Assistant II provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, conducting specific assessments, and timely completion of data entry and query resolution for CRFs.
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Essential duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely data entry and query resolution for CRFs.
$21 - $25 / HOUR
The Patient Liaison Specialist acts as a representative for patients and their families, directing queries and complaints to relevant healthcare professionals while consulting with providers to evaluate patient progress. Essential duties include meeting with patients to discuss care quality, communicating concerns to staff, explaining policies, and informing families about treatment progress.
$19 - $20 / HOUR
3 months ago
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties involve creating and maintaining patient charts, preparing for participant visits, timely data entry, and assisting coordinators with various assessments and clerical tasks.
The role involves performing various clinical and neurocognitive test evaluations, interviews, and ratings on study participants according to the protocol, including administering and scoring tests related to cognitive, neuropsychological, behavioral, and emotional status. Essential duties also include completing clinical intake forms, assessing subject eligibility, interacting with the medical monitor, and ensuring subject safety throughout the study duration.
$85,000 - $125,000 / YEAR
The Pharmacy Technician I will assist in supporting clinical investigational drug trials by accurately and efficiently dispensing medication under moderate oversight. Key duties include monitoring pharmacy activities for protocol adherence, preparing blinded study products, and ensuring proper storage of investigational drugs according to FDA guidelines.
$19 - $23 / HOUR
