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Remote 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
Research Analyst-Project Coordinator (Remote)
By Talentify.io At United States
Strong organizational and time management abilities.
Proficiency in project management software.
Knowledge in areas such as early intervention, special education, educational equity, and program evaluation.
Experience in an education organization or agency.
Strong systems thinking and understanding of project management strategies.
Contribute to research, training, and technical assistance activities in the education field.
Clinical Research Analyst *Remote*
By Talentify.io At United States
Communicate extensively with various stakeholders to manage research activities including billing compliance, budgeting, subject tracking, data collection, and sponsor invoicing.
Bachelor's Degree in a health-related field or 4 additional years of related experience.
Three years of IRB, regulatory, or research experience (4 years preferred).
Three years of relevant CTMS experience.
This is a remote position that can be based in any Providence state approved location in the US.
Review clinical research protocol documents and replicate the protocol schedule of events in Velos EResearch CTMS.
Coord,Clinical Research Ii - 100% Remote
By Talentify.io At United States
Track and maintain study-related information in the data management system
Ensure adherence to study protocols and regulatory requirements
Bachelor's degree in a scientific or health-related field, or equivalent experience
1-3 years of related experience
Obtain consent of research participants in accordance with IRB approved protocols and regulations, including HIPAA
Schedule and conduct participant study visits, tests, interviews, and telephone follow-up calls
Clinical Research Trainer - Remote ($59000.00 - $91500.00 / Year)
By Talentify.io At United States
Deliver engaging and logical CRA-sponsored training remotely
Excellent planning and prioritization skills aligned with organizational goals
Develop and update CR education tools and course materials
Schedule MSK-wide CR educational courses for staff
High School Diploma and 2-5 years of relevant experience in training, mentorship, or clinical research
Knowledge of training design, medical terminology, and oncology concepts preferred
Research Specialist - Remote
By Talentify.io At United States
Opportunity to work with a full-service consulting firm that blends creative thinking with technical skills
Remote work with occasional travel to client office in Rockville, MD
Master's degree in behavioral or social science and 2+ years of experience in quantitative research field
US Citizenship required as part of client contract requirement
Experience supporting senior-level Federal civilian client and managing programs for a federal client
Strong organizational and statistical analytical skills
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 Monitor (Remote, Southwest Region) Tmtt
By Edwards Lifesciences At Pueblo-Cañon City Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
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 Associate - Southeast (Remote) ($88480.00 - $139100.00 / Year)
By Talentify.io At United States
Skilled in calendar management and scheduling
Knowledge of internet marketing including email and forum management
Possess strong administrative and organizational skills
Ability to multitask and perform data entry and analysis
Experience in minutes and notes taking
Knowledge of telephone and conference calling
Clinical Research Associate - Southeast Region (Remote) ($88480.00 - $139100.00 / Year)
By Talentify.io At United States
Develop and implement contract management policies and procedures
Manage contracts, global IP portfolio, and litigation matters
Register copyrights and manage annuity payments
Manage all aspects of legal holds and maintain reporting on litigation matters
Manage relationship with insurance providers about claims
Completion of paralegal school/certification highly desired
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.
Research Analyst - Clinical Research - Remote
By Talentify.io At United States
Strong organizational and time management ability.
Manage the study website, update content, and respond to queries from external investigators and NIH clients.
Prepare documents and power points, draft reports, and manage IRB submissions for multiple sites.
Minimum of 2 years of job experience in clinical/scientific research.
Excellent communication and collaboration skills.
Support research committees by organizing virtual and in-person meetings, preparing agendas, materials, meeting minutes, and action items.
100%Remote Role || Clinical Research Specialist
By Cloud Space LLC At United States
Skills & Experience (top 3 skills):
•Quality Management System/Regulatory Compliance Program
Location:100% remote – EST support Henry Ford in Detroit (Remote)
Work Experience (do not edit):
•Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Insert major accountabilities in chart
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.
Research Associate - Communications Coordinator - Remote ($63100.00 - $74800.00 / Year)
By Talentify.io At United States
A minimum of 5 years of demonstrated experience with project coordination and/or project management.
Working experience with content management.
Organization skills, including time management ability
Collaboration with teams, managers and/or clients
Subject To Plan Requirements, Employees May Participate In
Provide logistic support to meet various client requests.

Are you looking for a rewarding career in clinical research? We are seeking a Remote Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, ensuring compliance with regulatory standards, and providing support to research teams. If you are passionate about making a difference in the medical field, this is the perfect opportunity for you!

Overview A Remote Clinical Research Coordinator is responsible for coordinating and managing clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. Detailed Job Description The Remote Clinical Research Coordinator is responsible for the coordination and management of clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. The Remote Clinical Research Coordinator is also responsible for the development and implementation of research protocols, the collection and analysis of data, and the preparation of reports and presentations. The Remote Clinical Research Coordinator must be able to work independently and collaboratively with other team members. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to work independently and collaboratively
• Excellent organizational and communication skills
• Proficiency in data analysis and reporting
• Ability to manage multiple projects simultaneously
• Knowledge of computer systems and software
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Knowledge of Good Clinical Practice (GCP)
• Ability to work in a remote setting
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of computer systems and software
Job Experience
• At least two years of experience in clinical research
• Experience in data analysis and reporting
• Experience in project management
Job Responsibilities
• Develop and implement research protocols
• Collect and analyze data
• Prepare reports and presentations
• Manage multiple projects simultaneously
• Ensure compliance with clinical research protocols and regulations
• Communicate with clinical research teams, sponsors, and other stakeholders
• Work independently and collaboratively with other team members