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Clinical Research Scientist I Jobs in San Mateo, California

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 Associate I
By Nevro Corp. At , Redwood City, 94065, Ca $67 an hour
2 years of related experience in supporting medical device clinical trials
Strong interpersonal and communication skills
Able to manage multiple tasks
Experience working directly with US and EU sites strongly desired
Experience working with clinical data and databases (desirable)
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
Clinical Research Associate I
By Nevro At Redwood City, CA, United States
2 years of related experience in supporting medical device clinical trials
Strong interpersonal and communication skills
Able to manage multiple tasks
Experience working directly with US and EU sites strongly desired
Experience working with clinical data and databases (desirable)
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
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.
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 - Smidt Heart Institute
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1-year Clinical Research Related Experience
Join our team and use your skills with an organization known nationally for excellence in research!
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Research Scientist I Jobs
By Public Health Institute At , Sacramento, Ca $80,043 - $118,302 a year
Three years of relevant research and/or evaluation experience.
Bachelor’s degree required, or substitute with four additional years of related experience.
Intermediate to advanced skills in MS Office Word, Excel, and PowerPoint.
Research or evaluation experience with quantitative statistical software, such as SAS, SPSS, or R.
Demonstrated abilities of independent work, scientific reasoning, verbal presentation of scientific data, and production of written reports and/or scientific publications.
Substantial experience with evaluation-related technical assistance to local agencies.
Research Scientist I Jobs
By Public Health Institute At Greater Sacramento, United States
Three years of relevant research and/or evaluation experience.
Bachelor’s degree required, or substitute with four additional years of related experience.
Intermediate to advanced skills in MS Office Word, Excel, and PowerPoint.
Research or evaluation experience with quantitative statistical software, such as SAS, SPSS, or R.
Demonstrated abilities of independent work, scientific reasoning, verbal presentation of scientific data, and production of written reports and/or scientific publications.
Substantial experience with evaluation-related technical assistance to local agencies.
Clinical Research Associate I - Regenerative Medicine Institute
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
Understanding of general clinical research objectives. One (1) year of clinical research experience is preferred.
Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations.
Must possess computer skills, including Word and Excel, and the ability to use standard office equipment is required.
Assists with clinical trial budgets and patient research billing.
Completes Case Report Forms (CRFs).
Clinical Research Associate I Prdm
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Clinical Research Associate I, Rosser
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1 year of Clinical Research Related Experience preferred
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Clinical Research Data Specialist I - Cedars-Sinai Center For Outcomes Research And Education (Cs-Core) - Part-Time
By CEDARS-SINAI At , Los Angeles, Ca $23.39 - $39.76 an hour
Participates in required training and education programs.
Experience in a similar position is highly preferred.
Maintains the accuracy, integrity and security of complex, large computerized records systems.
Understands regulations, policies, protocols, and procedures to control and maintain accurate records.
Performs data searches and other related administrative tasks.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Clinical Research Specialist I
By Cedars-Sinai At Los Angeles, CA, United States
May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
Participates in required training and education programs.
Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution.
Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
Coordinates research projects at an institutional or departmental level.
Communicates project status and improvement areas with leadership in a timely manner.
Clinical Research Scientist Jobs
By Johnson & Johnson At Milpitas, CA, United States
Represent Clinical Science in cross-functional project team meetings, provide project team requirements as needed, with input/guidance from senior function members.
Align with Clinical Operations team (study managers, CRAs) on project status/updates and identify issues or impact to project timelines as appropriate.
At least 6 years of work experience
Experience in clinical or scientific research
Experience in class III medical device research
Solid understanding of industry regulatory and compliance requirements
Clinical Research Coordinator I, Strive & Bhs
By Tulane University At , Bogalusa, La
Strong communication skills both verbal and written, report writing, and ability to meet deadlines
Good team member and experience in working in an office environment
LPN with current state licensure at the time of hire and three (3) years of related work experience
Experience working on a research study or clinic is preferred, but not required
Experienced with research coordination and teams
Ability to acquire and maintain all required CITI training certificates
Research Scientist I Jobs
By Exact Sciences Corporation At , San Diego, Ca $90,000 - $144,000 a year
Support and comply with the company’s Quality Management System policies and procedures.
Basic knowledge of statistical and mathematical methods in biology/genetics/genomics; including experience with statistical software, such as JMP.
Assist in collection, documentation, communication, and review of product requirements.
Strong attention to detail skills.
Excellent analytical, problem solving, and decision-making skills.
Apply technical knowledge, scientific creativity and rigor, collaboration with others, and independent thought; ability to provide insights and defend scientific ideas.
Clinical Research Associate I
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1 year Clinical Research Related Experience
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Clinical Research Specialist I - Clinical Research Office
By Cedars-Sinai At Beverly Hills, CA, United States
Maintains all DSMC required documentation and ensures accurate recording of DSMC reviews into the clinical trial management system (OnCore).
Works with CCTO management to establish and optimize metric reports.
Assists in management of SOCCI Protocol Review and Management Committee by serving as a backup when necessary.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law. Participates in required training and education programs.
3 years of related experience in a similar position is required.
Prior monitoring or auditing experience in clinical research preferred.
Clinical Research Coordinator I
By Children's Hospital Los Angeles (CHLA) At Los Angeles, CA, United States

NATIONAL LEADERS IN PEDIATRIC CARE

Clinical Research Associate I - Regenerative Medicine Institute
By CEDARS-SINAI At , Los Angeles, Ca $17.57 - $29.87 an hour
Participates in required training and education programs.
Understanding of general clinical research objectives. One (1) year of clinical research experience is preferred.
Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations.
Must possess computer skills, including Word and Excel, and the ability to use standard office equipment is required.
Assists with clinical trial budgets and patient research billing.
Completes Case Report Forms (CRFs).

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