Research Scientist I Jobs
By Elinor Coatings, LLC At Fargo, ND, United States
[Perform root cause analysis, troubleshoot issues, and manage multiple projects to meet deadlines]{gill="" sans="" mt\",sans-serif\"=""}
[3+ years of experience in a laboratory environment]{gill="" sans="" mt\",sans-serif\"=""}
[Demonstrated experience with:]{gill="" sans="" mt\",sans-serif\"=""}
[Communication and writing skills to enable working with multi-disciplinary groups of individuals]{gill="" sans="" mt\",sans-serif\"=""}
[Conduct protective coating formulation, testing, and corrosion evaluation for customer trials and RandD projects]{gill="" sans="" mt\",sans-serif\"=""}
[Generate, document, and report data and technical progress to internal and external stakeholders]{gill="" sans="" mt\",sans-serif\"=""}
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
Translational Research Scientist - I (Assistant)
By Pacer Staffing LLC At South San Francisco, CA, United States

Qualifications Bio-conjugation Scientist Role. Qualifications: Education Requirement: Minimum qualifications include a B.S./M.S/ PHD in chemistry, biochemistry, or related field, with industrial or ...

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.
Research Scientist I Jobs
By Research Foundation for Mental Hygiene, Inc. At New York, NY, United States

Lab management: Manage purchases and equipment maintenance service contracts.

Present data at meetings and write papers.

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 Laboratory Scientist I
By Charles River Laboratories At Los Angeles, CA, United States
High school diploma or comparable education is required.
At least 1 year of previous CLS working experience.
Blood donor center or transfusion service experience is a plus.
Accurately perform testing of blood products and donor samples (i.e., hematology counts (CBC), and pH).
Accurately record, interpret, and report test results. Ability to recognize and appropriately handle unacceptable test results.
Verify acceptability of blood samples.
Research Scientist I, Biostatistician
By Kaiser Permanente At , Pasadena $141,500 - $183,040 a year
Must be able to work in a Labor/Management Partnership environment.
Serves on and may Chair R&E&SCPMG committees based on experience and expertise.
Mentors junior faculty when experience and opportunities permit.
Doctoral degree (Ph.D.) in biostatistics OR eight (8) years of experience in a directly related field.
High School Diploma or General Education Development (GED) required.
Professional experience (years dependent on rank) in designing and conducting original research and publishing in peer review journals.
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.
Research Scientist I Jobs
By Sony Electronics At , San Jose $170,000 a year
Conduct research on computer vision algorithms with label efficient training methods (e.g. object detection, pose estimation).
Write journal papers, and submit patents applications if necessary
EEO is the Law Supplement
Clinical Research Scientist Jobs
By Seattle Childrens Hospital At , Seattle, 98105 $89,794 - $134,680 a year
Minimum of four (4) years of related research experience.
Advanced degree in scientific related field (Master's, PhD, MD).
Min to Max Annual Salary$89,793.60 - $134,680.00 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Seattle Children's is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.
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 Scientist I Jobs
By Medical College of Wisconsin At , Milwaukee, 53226
Knowledge of standard experimental and computational structural biology techniques, protein biochemistry, molecular biology, documentation, and records management.
Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Appropriate experience may be substituted for education on an equivalent basis
Coordinate research study activities; lead and manage projects.
Minimum Required Education: PhD in physical or biological sciences
Minimum Required Experience: 0 years
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 ...

Senior Research & Development Scientist I
By Chobani At , Twin Falls $84,800 - $127,200 a year
1 year of experience with Lean product development, and statistical analysis;
5 years of experience with basic research tools, statistical analysis, product and process development; and
Maintain pilot plant equipment utilized to manufacture pilot bench top samples;
Be able to multitask on many projects, recognizing and adhering to adjusting priorities and deadline;
Proactively solve complex issues, identifying potential solutions and process improvement opportunities;
Utilize statistical software to generate experiment design, execute experiments, collect and analyze relevant data, with little oversight; and
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.
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.
Clinical Research Associate I, Dcri
By Duke University At , Durham, 27710
Review education and training experience with line manager and complete identified training needs within designated time period.
*Basic knowledge of site management and clinical monitoring for clinical research studies
Maintain job knowledge and skills through independent self-study.
OR EQUIVALENT COMBINATION OF EDUCATION AND EXPERIENCE
None required beyond that described above. OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE
Perform assessment of site personnel and facilities for study conduct through feasibility and site telephone qualification
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

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Scientist I to join our team and help us develop innovative treatments for a variety of diseases. As a Clinical Research Scientist I, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will also be involved in the development of new therapeutic strategies and the evaluation of existing treatments. If you are passionate about making a difference in the lives of patients, this is the job for you!

Overview Clinical Research Scientist I is a professional who is responsible for conducting clinical research studies and trials. They are responsible for designing, planning, and executing clinical research studies and trials, as well as analyzing and interpreting the data collected. They also provide guidance and support to other clinical research professionals. Detailed Job Description Clinical Research Scientist I is responsible for designing, planning, and executing clinical research studies and trials. They are responsible for developing protocols, collecting and analyzing data, and preparing reports. They also provide guidance and support to other clinical research professionals. They are responsible for ensuring that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines. Job Skills Required
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to analyze and interpret data
• Ability to manage multiple projects simultaneously
• Proficiency in computer applications
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (e.g., CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and methods
• Knowledge of regulatory requirements and guidelines
• Knowledge of medical terminology
• Knowledge of clinical trial design and implementation
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in designing, planning, and executing clinical research studies and trials
• Experience in analyzing and interpreting data
• Experience in preparing reports
Job Responsibilities
• Design, plan, and execute clinical research studies and trials
• Develop protocols and collect data
• Analyze and interpret data
• Prepare reports
• Provide guidance and support to other clinical research professionals
• Ensure that all clinical research studies and trials are conducted in accordance with applicable regulations and guidelines