Register
Recruit Create CV

Research Clinical Coordinator Jobs in Union, Arkansas

Clinical Coordinator Jobs
By Valleywise Health At United States
Requires four (4) years of experience providing mental health services that demonstrates an understanding of the required knowledge, skills and abilities.
Requires extensive knowledge and/or previous experience with the ACT service delivery model.
Prefer prior direct or indirect supervisory experience.
Must be able to communicate effectively and have excellent customer service skills.
Must possess solid analytical and problem-solving skills.
Requires a Master's degree in a Behavioral Health 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.
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.
Research Coordinator Jobs
By Georgia College & State Univ At , State Univ, Ar $47,476 - $50,000 a year

About Us Georgia College & State University is the state's designated public liberal arts university. As a member of the prestigious Council of Public Liberal Arts Colleges (COPLAC), ...

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 Coverage Analyst
By Medix™ At United States
● Knowledge of clinical research protocol management.
Job Summary & Preferred Qualifications:
● Certification in Health Research Compliance preferred.
● Experience with institutional research activity billing compliance with all
● Knowledge of clinical research budgeting.
● Experience with Oncore preferred
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
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-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
Clinical Research Manager Jobs
By Masis Professional Group At United States
Minimum of 5 years' experience working in a Clinical Research Manager or Clinical Project Manager role with relevant experience.
Experience with FDA and US requirements for the conduct of clinical studies is a must.
Multi-disciplinary international project management managing diverse relationships.
Exciting job opportunity with project responsibilities and freedom for professional growths and acquisition of new skills
Supervision (remote and in-person) of participating study centers
Ability to manage multiple projects in parallel and prioritize across study, regulatory, and company goals.
Research Coordinator, Nigeria Jobs
By 60 Decibels At United States
Lead day-to-day management of remote Research Assistant teams across different regions
Ability to juggle multiple tasks; proven self-starter, proactive problem-solver with strong communication and project management skills
Ensure data collection timelines are met through proactive planning and problem-solving as well as management of Research Assistants and third-party partners
3+ years of relevant professional experience; candidates with experience managing data collection, field operations or agent networks strongly preferred
Ensure complete, accurate, clean and consistent data is collected and shared with project teams for analysis and reporting
Communicate project updates both in various project channels on Slack, and with Research Assistants reliably and consistently
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 Engineer Jobs
By OrganOx At United States
· Knowledge of project management tools and practices
· Experience with perfusion devices and management of patients or donor organs is a must
· Identify and report study protocol challenges and compliance issues to clinical management
Responsibilities may include the following and other duties may be assigned:
· Experience in a clinical setting and clinical studies is beneficial
· Excellent presentation and computer skills

Are you looking for an exciting opportunity to make a difference in the lives of patients? We are seeking a Clinical Coordinator to join our research team and help us develop innovative treatments for a variety of medical conditions. As a Clinical Coordinator, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements, and providing support to research staff. If you are passionate about making a difference in the lives of patients, this is the perfect job for you!

Overview Research Clinical Coordinators are responsible for coordinating and managing clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. Detailed Job Description Research Clinical Coordinators are responsible for the planning, implementation, and management of clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. They must also ensure that all research results are accurately reported and that all research activities are conducted in compliance with applicable laws and regulations. Job Skills Required
• Excellent organizational and communication skills
• Ability to manage multiple projects and tasks simultaneously
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Ability to work independently and as part of a team
• Ability to work with a variety of stakeholders
• Ability to analyze and interpret data
• Knowledge of budgeting and financial management
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research or related field (preferred)
Job Knowledge
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Knowledge of budgeting and financial management
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in recruiting and training research staff
• Experience in managing research budgets
• Experience in ensuring regulatory compliance
Job Responsibilities
• Plan, implement, and manage clinical research projects
• Ensure that all research protocols are followed
• Collect and analyze data accurately
• Ensure that research is conducted in a safe and ethical manner
• Recruit and train research staff
• Manage research budgets
• Ensure that all regulatory requirements are met
• Report research results accurately
• Ensure that all research activities are conducted in compliance with applicable laws and regulations