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Research Clinical Coordinator Jobs in Maryland

Clinical Research Coordinator Jobs
By CAMRIS At Bethesda, MD, United States
Knowledge of clinical quality management and systems (such as Veeva, Master Control, etc.) is preferred.
Assist in the management of Division contract records. Tasks include the following:
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at
Minimum of five (5) years of experience in clinical research or a related field.
Excellent communication, grammar and writing skills required.
Demonstrated superior knowledge of research protocols and clinical, scientific and/or medical terminology.
Clinical Research Coordinator Jobs
By Axle Informatics At Rockville, MD, United States
Supports the creation and management of clinical websites and web-based tools.
Manages conflicts issues that arise in clinical research setting, by utilizing strong communication and collaboration skills.
Educational Benefits for Career Growth
Assist researchers with study testing, observations data entry and other duties associated with study sessions. 5
Assesses ongoing consent through discussions with participants and reinforcement of education
Create mock ups and visualizations to illustrate to web developers how to execute web enhancements or new web requirements.
Outpatient Services Coordinator (Clinical Research)
By Pharmaron At Baltimore, MD, United States
Works with management to develop optimal workflow of screening activities.
Maintain knowledge of protocols and general operation of the unit.
Coordinates with other departments in preparing study screening documentation.
Conducts screening activities of potential subjects.
Assists with Outpatient follow-up visits.
Performs administrative tasks to support team members with clinical trial execution as needed.
Research Coordinator - Neurogenetics Research
By Kennedy Krieger Institute At Baltimore, MD, United States
Two years’ experience working in a human subject research or clinical care environment involving genetics,
Previous professional experience with multi-site and investigator-initiated research protocols.
Attending study-related meetings, conferences, teleconferences, as well as participating in any additional planning- and development-related activities, as needed.
Responsible for data analysis which includes performing statistical analyses, presentation of results, and initial data interpretation.
Assistance with preparation of trial/study related materials progress reports, and any other research execution/implementation pertinent documentation.
Will work closely with Principal Investigator in developing and implementing standard operating procedures.
Coordinator, Research Project Jobs
By University of Maryland, Baltimore At , Baltimore, Md $44,000 - $52,000 a year
Knowledge of all applicable requirements, regulations, and laws.
May supervise those who perform data entry and perform non-routine data analysis.
Skill in effective use of applicable technology/systems.
Develop and produce reports of study data for project staff and stakeholders.
Obtains, processes, and transports specimens to the appropriate laboratory according to established aseptic technique.
Performs venipunctures and finger sticks to obtain blood specimens.
Clinical Research Specialist Jobs
By University of Maryland Medical System At Baltimore, MD, United States
Reports adverse events and near misses to appropriate management authority.
Skill in statistical programming, interpretation and data analysis using statistical software as well as spreadsheet and database software applications.
Ability to apply knowledge of scientific theory and computer capability to design and recommend changes to methods for clinical research.
Knowledge of best practice in Clinical Research.
Recruit and screen subjects for research studies.
Perform administrative duties such as providing training and guidance to other clinical research staff.
Clinical Protocol Coordinator Jobs
By Axle Informatics At Rockville, MD, United States
Help to maintain a project management plan encompassing planning, tracking, execution, and completion of activities for all tasks.
Must demonstrate a history of proven success in study management
Educational Benefits for Career Growth
Assist staff to establish standardized infrastructure and procedures for recruitment and follow-up while accommodating site-specific requirements.
Assist researchers collect, organize and maintain all study documentation to include investigator qualifications, trial logs, and safety reports.
*Willing to accept candidates both local and remote - max flexibility permissible.
Clinical Research Coordinator Jobs
By Massachusetts General Hospital(MGH) At , Charlestown, 02129, Ma
Experience working with individuals with ASD.
Experience with the ADOS assessment of ASD.
Research coordination experience via internship or otherwise.
Experience with administering psychological assessments.
Experience with Excel, and Microsoft office more generally
Outstanding telephone and oral / written communication 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