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Research Clinical Coordinator Jobs in 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 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
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.
Research Coordinator Jobs
By QUALITY EDUCATION FOR MINORITIES NETWORK At Washington DC-Baltimore Area, United States
Strong verbal and written communication skills
Strong organizational skills and attention to details
Experience working with the Indigenous community
Previous experience in an office setting
Previous experience in a team-based environment
Experience with meeting rigid deadlines
Research Coordinator Jobs
By Vacasa At United States
Please visit our careers page to review our full benefits offerings
GIS experience is a bonus!
Employer Sponsored & Voluntary Supplemental Benefits
Locate and search local planning and zoning codes for STR regulation information
Present STR regulation information researched to applicable stakeholders
Keep track of updating regulations around the country and notify teams of changes
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 Specialist Jobs
By Roth Staffing At United States
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Must have knowledge in reference to good clinical practices regulations and standard operating procedures.
The job requires the ability to make judgements based on practice and previous experience.
Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.
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

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