- Comprehend study design of each protocol that is assigned
- Perform procedures in compliance with the study protocol
- Recruit and screen study subjects according to specific protocol requirements
- Collect and record study data in source documents via electronic system (CRIO)
- Manage study related activities
- Adherence to protocol requirements
- Review laboratory data
- Assess and document compliance
- Manage investigational product
- Assess, record, and report Adverse Events as outlined in the protocol
- Manage/train ancillary staff
- Experience and training in conducting clinical trials with knowledge of ICH GCP
- Two years of college in a health-related program or LPN
- Bachelor's degree in a health or scientific related program
- A thorough understanding of regulatory requirements
- Excellent interpersonal and communication skills: Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Experience with CRIO (Clinical Trial Management System) is a plus
- Experience with administering vaccines is a plus
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Johns Hopkins University Baltimore, United StatesThe Department of Child and Adolescent Psychiatry is seeking a **_Research Program Coordinator_** to coordinate various research projects in the Johns Hopkins Division of Child and Adolescent Psychiatry related to mental health interventions in community settings. Projects includ ...
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Research Project Coordinator
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Research Program Coordinator
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Johns Hopkins University Baltimore, United StatesThe Department of Neurology is seeking a **_Research Program Coordinator_** who will coordinate clinical trials and other clinical research projects in the Johns Hopkins Multiple Sclerosis Center. This may involve, but is not limited to data monitoring, screening medical records, ...
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Research Program Coordinator
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Research Program Coordinator
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Research Program Coordinator
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Johns Hopkins University Baltimore, United StatesThe Department of Neurology is seeking a **_Research Program Coordinator _**to join the Brain Health Program in the division of Neuroimmunology & Neurological Infections. In this role, the coordinator will be responsible for implementing clinical research related to understanding ...
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Research Program Coordinator
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Johns Hopkins University Baltimore, United States**Specific Duties and Responsibilities** · - Assist the Principal Investigator in aspects of clinical research such as assisting in starting and conducting a clinical trial. · - Responsible for Data Management for Seizure device and drug trials. · - Assist the Principal Investiga ...
Clinical Research Coordinator - Pikesville, United States - Headlands Research
Description
OverviewAt Headlands Research, we are building a best in class clinical trial network.
We're an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 18 clinical trial sites in the US and Canada with rapid plans for expansion.
The RolePharmasite, a Headlands Research site, is looking for a Clinical Research Coordinator to manage clinical research protocols.
This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
ResponsibilitiesEducation: