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Clinical Research Coordinator Jobs in Arkansas

Clinical Research Coordinator (Part-Time) - Tisch Cancer Institute
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
0-2 years of experience in a hospital or academic (research) environment preferred.
Excellent written and oral communication skills
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Clinical Research Coordinator Ii-Psychiatry - Ism - Ft - Day
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator I - Neurology
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Coordinator I - Tisch Cancer Institute
By Mount Sinai Health System At United States
Assists with coordination and management of clinical trials including communication with Sponsors.
Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.
1-2 years of research experience
Experience in a hospital or academic (research) environment preferred
Excellent written and oral communication skills
Collects and records study data; inputs all information into database.
Clinical Research Coordinator I
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Coordinator - Hybrid/Remote - 122856 ($33.60 - $43.81 / Hour)
By Talentify.io At United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
Strong knowledge of investigational protocols especially with pediatric protocols (data management, query resolution, protocol design, protocol writing and protocol implementation).
Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
Experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Clinical Research Regulatory Coordinator
By Medix™ At United States
Experience using standard word processing and data management software programs, including Word and Excel, in order to develop and prepare reports.
Experience creating Informed Consent Documents that comply with HRPP/ IRB policies and procedures, FDA regulations, and sponsor requirements.
Experience with editing, including summarizing information into concise and condense documents.
Knowledge of oncology and hematology.
Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research.
Working knowledge of Human Research Protections Program (HRPP/IRB) policies and Procedures.

Are you looking for an exciting opportunity to make a difference in the medical field? We are seeking a Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, coordinating patient visits, and ensuring compliance with regulatory standards. If you have a passion for helping others and a commitment to excellence, this could be the perfect job for you!

A Clinical Research Coordinator (CRC) is responsible for the coordination and management of clinical trials and research studies. They are responsible for ensuring that the research is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP).

What is Clinical Research Coordinator Skills Required?

• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of medical terminology
• Knowledge of clinical research regulations and guidelines
• Proficiency in computer applications
• Ability to manage multiple tasks and prioritize
• Ability to work in a fast-paced environment

What is Clinical Research Coordinator Qualifications?

• Bachelor’s degree in a health-related field
• Certification in clinical research (CCRC)
• Previous experience in clinical research

What is Clinical Research Coordinator Knowledge?

• Knowledge of clinical research protocols
• Knowledge of clinical trial design and data management
• Knowledge of medical terminology
• Knowledge of Good Clinical Practice (GCP)

What is Clinical Research Coordinator Experience?

• Previous experience in clinical research
• Previous experience in data management
• Previous experience in clinical trial design

What is Clinical Research Coordinator Responsibilities?

• Develop and implement clinical research protocols
• Monitor clinical trial progress and data
• Ensure compliance with applicable regulations and GCP
• Prepare and submit regulatory