Clinical Research Coordinator I
By Emory University At , Atlanta, 30322
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Assists with patient recruitment. Attends study meetings.
Clinical Research Coordinator I
By Morehouse School Of Medicine At , Atlanta, 30310, Ga
Improve the health and well-being of individuals and communities;
Increase the diversity of the health professional and scientific workforce;
You will find a fulfilling career at
Clinical Research Coordinator I
By Emory University At , Atlanta, 30303, Ga
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Orders and maintains equipment and supplies.
Clinical Research Coordinator I
By The Geneva Foundation At , San Antonio, 78234 $43,800 - $58,800 a year
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Knowledge of CFR, GCP and ICH guidelines
Promote safety and confidentiality of research participants at all times
Clinical Research Assistant I-Ebrahimi-Fakhari Lab
By Boston Children's Hospital At , Boston, 02115, Ma
Develop skills in project coordination, data management, and regulatory compliance
Gain experience in conducting clinical research in a multi-center setting
Manage a central clinical database, biobanking of biosamples, and a genome archive
Prior experience in clinical research is preferred but not required
Strong organizational and communication skills
Engage in close collaboration with patients and families, particularly in the context of rare diseases
Clinical Research Assistant I, Pediatric Er Division
By UT Southwestern At , Dallas, 75390, Tx

May perform some or all the following based on research study:

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Clinical Research Assistant I, Psychiatry
By UT Southwestern At , Dallas, 75390, Tx

Experience and Education High School diploma or GED with no experience. A minimum of Heart Saver for non-licensure or BLS for Licensure may be required based on research study protocols or affiliate ...

Research Animal Specialist I
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Provide compliance monitoring of cage conditions. (Overcrowded cage management, spot changing of dirty cages, etc.).
For more information regarding MGH and the extensive benefits package offered to employees, visit: https://www.massgeneral.org/careers
SKILLS / ABILITIES / COMPETENCIES REQUIRED:
Experience in care of animals preferred.
Ability to learn and use bar code/PDA technology and basic computer skills including email and Microsoft Outlook.
The Following Duties may be performed daily under supervision from the Team Lead or Manager:
Temporary Clinical Research Assistant I
By UT Southwestern At , Dallas, 75390, Tx

Why UT Southwestern? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and ...

Clinical Research Assistant I, Neurology
By UT Southwestern At , Dallas, 75390, Tx

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Clinical Research Assistant I
By Boston Childrens Hospital At , Boston, 02115, Ma
One year of relevant work experience is preferred.
Analytical skills to gather and interpret data in which the information or problems are moderately complex to complex.
Working alongside Investigators and collaborators to assist in the start-up and conduct of studies;
Participating in the development of study manuals and other study-related documents;
Assisting the Research Coordinators with IRB applications, preparing amendments and continuing reviews for each study and for each participating site;
Facilitating the scheduling and organizing of calls with Investigators, Research Coordinators and Vendors as needed;
Clinical Research Assistant I, Psychiatry, Mood Disorders
By UT Southwestern At , Dallas, 75390, Tx

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Clinical Research Assistant I-Otolaryngology
By Boston Childrens Hospital At , Boston, 02115, Ma
Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study.
Monitor and reviews data collection and data entry, and informed consent procedures ensuring consistency of application for each study.
Analytical skills to gather and interpret data in which the information or problems are moderate to complex.
Consent and recruit patients for research studies through personal interviews and written communications with patients/families.
Provide details to families with detailed background information regarding studies communicate all policies and procedures, and respond to all inquiries.
Coordinate follow-up visits as necessary.
Clinical Research Assistant I Neurology Domd
By Brigham & Women's Hospital(BWH) At , Boston, 02115, Ma
High degree of computer literacy and ability/willingness to learn basic website management skills. Coding skills highly desirable.
Knowledge of data management programs.
Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies.
Assists PI or Research Manager with preparation for presentation and written published articles; there are opportunities to communicate research to colleagues.
Prior experience in the clinic or clinical research is highly desired.
At least one year of work experience in a research setting. Sound independent judgment and competence in research methodologies.
Clinical Research Assistant I (Crci), 40 Hours, Bwh Connors Center For Women’s Health
By Brigham & Women's Hospital(BWH) At , Boston, 02115, Ma
Experience with clinical/psychological research, including recruiting research participants and using electronic data management software.
Working knowledge of literature searches & using reference management software
Assisting with literature reviews and reference management for grant submissions
Experience with PowerPoint and Excel.
Experience with data collection, preferably in clinical setting.
Prior experience working or volunteering in a large, academic research center.
Clinical Research Assistant I- Medicine And Immunology
By Boston Childrens Hospital At , Boston, 02115, Ma
Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study.
Monitor and review data collection, data entry, and informed consent procedures, ensuring consistency of application for each study.
Consent and recruit patients for research studies through personal interviews and written communications with patients/families.
Provide detailed background information regarding studies to families, communicate all policies and procedures, and respond to all inquiries.
Coordinate follow-up visits as necessary.
Act as a resource to study participants, addressing their concerns.
Clinical Research Specialist Jobs
By Enloe Medical Center At , Chico, 95926, Ca $22.92 - $26.93 an hour
Knowledge of Federal and State regulatory issues/mandates concerning Institutional Review Board requirements
This position has potential to work remotely (must live in California).
Two years’ experience with Word, Excel and Internet access/use
Previous experience with clinical research
BS/BA degree in health sciences or related field
Formal training in decision support, databases, spreadsheet, report writer, query/relational database computer software applications
Clinical Research Support Specialist
By Ann & Robert H. Lurie Children's Hospital of Chicago At Streeterville, IL, United States
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Student loan servicing and support
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children’s facilities
Research Data Specialist I
By California Department of Justice At California, United States
Collaborate with management and research specialists to develop data collection methods,
Experience with statistical packages, such as SPSS or SAS.
Experience with independent research or being part of a research team.
**Benefits of working for the State of California**
Determine data sources and availability. Collect or extract data using a variety of established methods
Clinical Research Associate I- Principal
By i-Pharm Consulting At United States
Conduct all types of visits including, qualification, initiaiton, monitoring and close out
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
Minimum 1.5 years monitoring experience
Strong verbal and written communication skills
8-12 days on site per month
Clinical Research Coordinator I/Ii
By Fred Hutch At Seattle, WA, United States
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.
Clinical Research Lab Specialist
By AnMed Health At Anderson, SC, United States
Excellent computer and electronic database management skills.
Must possess excellent communication and interactive skills (both verbal and written), while also remaining flexible in responsibilities and work schedule.
Must maintain current certification for compliance and hazardous transport (IATA training).
Clinical Research, Data Associate I
By Castle Biosciences, Inc. At Phoenix, AZ, United States
Ability to multi-task and have good organizational and time management skills.
Experience in clinical research or the medical field preferred
Experience with Electronic Data Capture (EDC) systems, for the purpose of clinical research, preferred.
Experience with programming and coding (e.g., HTML and Java) required.
Possess excellent written and oral communication skills.
Critical thinking and problem-solving skills
Clinical Research Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
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 Specialist, (Irvine)- Thv
By Edwards Lifesciences At Irvine, CA, United States
Experience in clinical site monitoring, site qualification, and site educational training
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Experience in Medical device trial
Research Specialist I - Behavioral Health Research
By County of Riverside At Riverside, CA, United States
Hybrid remote work options are available but are subject to business needs and are not guaranteed.
Assists in the coordination with staff and outside agencies to obtain data; designs, organizes and develops research plans and evaluation designs.
Advises administrators of research findings and/or procedures; prepares narrative reports of findings with valid conclusions, projects program impacts, and predicts trends.
Riverside University Health System - Behavioral Health
Clinical Research Assistant I
By Beth Israel Deaconess Medical Center At , Boston
7. Assists investigator with correspondence with IRB. (essential)
4. Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
3. Potential exposure to adverse environmental conditions
o Several times a month: Radiation-irradiator possible.
Clinical/Translational Research Coordinator I - Asthma Research
By Vanderbilt University Medical Center At Nashville, TN, United States
Procures equipment and supplies needed to fulfill project requirements
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Specific Tasks and Skills Include But Are Not Limited To:
Communication (Fundamental Awareness): Clearly, effectively and respectfully communicates to employees or customers.
Discover Vanderbilt University Medical Center:
Research Specialist I Jobs
By Princeton University At , Princeton, 08542

Support existing code-base. Apply existing analysis tools on current unique dataset of family life

Analyze datasets. Implement deep conversation models on datasets. Implement deep image models on datasets

Clinical And Scientific - Research Scientist I
By Saviance At Johns Creek, GA, United States

Job Description: Major Accountabilities Performs polymer formulation and engineering in a research and development environment with minimum supervision Use relevant statistical techniques and ...

Clinical Research Data Entry Specialist I/Ii - Remote
By Frederick National Laboratory for Cancer Research At United States
Provides data entry and management support to an assigned caseload of research protocols
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
Reviews study protocols and assists in the planning and implementation of the data management aspects of clinical research projects
Possession of a Bachelor's degree from an accredited college/university, or qualifying experience in lieu of required education
Cloud–based clinical data management systems (e.g., Medidata Rave) and enrollment tracking systems (e.g., OPEN)
Works collaboratively with VRS team members, site staff, and data monitors to meet program and protocol requirements, deadlines, and deliverables
Clinical Research Specialist Jobs
By Össur At , Irvine
2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred
All training related to the quality management system is done in accordance to the Training Management Process.
Medical writer qualifications or Certified Research Associate a plus
Experience with both qualitative and quantitative research a plus
Strong collaborative and teamwork skills
We provide a flexible work environment to offer work/life balance
Clinical Procedure Specialist I
By B. Braun Medical Inc. (US) At United States
Prospects for and qualifies new leads through sales calls in person and remotely, via virtual channels.
Requires full working knowledge of relevant business practices and procedures in professional field.
Relies on experience and judgement to plan and accomplish assigned goals.
0-02 years related experience required.
Calls on clinical decision makers to position products for presentation, evaluation and purchase.
Develops and actively maintains a pipeline of sustainable new sales opportunities sufficient to achieve or exceed sales target/quota.