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Remote Clinical Research Coordinator Jobs in Union, Arkansas

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.
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
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 Program Coordinator, Employer Strategic Programs (Remote)
By One Medical At United States
Exposure to quality improvement or project management efforts
Troubleshoot issues related to these programs and triage questions from patients and providers
Serve as a liaison between the central team and local teams; provide feedback to continuously improve processes, communication and collaboration
Proficiency at MS Excel / Google Sheets
Paid sabbatical after 5 and 10 years
Employee Assistance Program - Free confidential advice for team members who need help with stress, anxiety, financial planning, and legal issues
Clinical Research Associate - South Region (Remote) ($88480.00 - $139100.00 / Year)
By Talentify.io At United States
Coordinates and manages various tasks in collaboration with other sponsor roles to achieve Site Ready
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines
Contributes to CRA Team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices
Invent | Pursue the Most Promising Internal and External Science to Address Significant Unmet Medical Needs
Execute | Prioritize Resources Behind Our Key Growth Drivers (Oncology, Vaccines, Select Specialty Areas, Animal Health) While Optimizing Our Base Business)
Adapt | Develop Our People, Culture and Business Model to Evolve with a Dynamic Landscape
Clinical Coordinator (Remote) Jobs
By MedCerts At United States
Manage the clinical placement process by determining site-specific requirements and communicate these to student in a timely manner
Bachelor’s Degree from a four-year college or university or equivalent combination of education and experience
Collaborate with MedCerts staff to resolve student concerns of clinical requirements
At least three years of closely related experience
Strong interpersonal and communication skills
Experience with design and implementation of business development strategy
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.
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

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