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Clinical Research Coordinator Jobs in Little Rock, Pulaski, Arkansas

Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Coordinator I-Iii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3-5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection
Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)
UAMS offers amazing benefits and perks
Part Time Clinical Research Coordinator
By Medasource At United States
3+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Must be available during business hours
Ensure data quality and integrity throughout the life of the study.
Collaborate with members of the research and care teams across MSK regarding data input.
Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
Clinical Research Coordinator I-Psychiatry-Msh-Ft-Day
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.
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.
Secures, delivers and ships clinical specimens as required by the protocol.
Clinical Research Coordinator (Dr. Jessica Robinson-Papp's Lab) - Neurology
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator Ii-Msh-Cs03-12118-013
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-Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.
Collect, process, deliver and ship clinical specimens as required by the protocol.
Clinical Research Coordinator-Msh/Qhc-14100-018
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator I-Emergency Med
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-12910-049
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 - Medicine Clinical Trials Office
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator, Part-Time-Emergency Medicine
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
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 in Science or closely related field.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator Jobs
By Advarra At United States
Remote, onsite, and hybrid opportunities available
Clinical Research Coordinators II/III roles are consulting (contractor) roles. These are not permanent position with benefits.
The benefits of enjoying the Advarra team include:
•Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Potentially higher hourly pay rate than working direct
Clinical Research Coordinator I (All Of Us)
By Mount Sinai Health System At United States
Strong communication and organization skills
Obtain informed consent and educate participants regarding study requirements.
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Background in clinical research or closely related field
Passion for patient care and clinical research
Clinical Research Coordinator - Seaver Center For Autism
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator I-Psychiatry-Ism-Ft-Day
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 Ii-13400-043
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 - Light & Health Research Center
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 - Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
Strong communication and organization skills
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.

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