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Clinical Research Specialist I Jobs

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.
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.
Solution Specialist, Safety, Clinical Research
By Verily At , Remote
10+ years of relevant experience in Enterprise sales or business development focused on SaaS, Real Word Data and scientific services.
Experience selling complex solutions and driving significant revenue growth.
Excellent communication, presentation and analytical skills.
Proven ability to work with complex, technical software and service offerings, and processes involving multiple stakeholders.
Experience with Google suite of productivity applications (gMail, gCalendar, Sheets, Slides, Docs).
Build and maintain strong relationships with customers and partners.
Dps Clinical Research Assistant I - Outcomes Research
By City of Hope At Duarte, CA, United States
Experience may substitute for minimum education requirements
Basic education, experience and skills required for consideration:
Preferred education experience and skills:
Conducts protocol management for an assigned set of multiple research protocols.
Performs data management and data analyses, as required by the research study.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.