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Clinical Research Data Specialist Jobs in California

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
Clinical Data Specialist Jobs
By Intellectt Inc At Alameda, CA, United States
At Least 3 years of experience in clinical data management and computer savvy. Some project management skills are needed.
Clinical data management experience needed.
They must be open to do menial tasks if they have 5 years experience.
Hybrid role (4 days onsite and 1 day remote)
A team player and flexible; quick and eager to enter into ADC.
Product: a sensor that will b put on the patient
Clinical Research Specialist Jobs
By Mindlance At Irvine, CA, United States
• Demonstrated experience in establishing and maintaining effective relationships with management, peers and subordinates and customers.
5) What are the top 5 skills/requirements this person is required have?
• Manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges.
a. Required Skill 1: Organized and great attention to detail
b. Required Skill 2: Strong communication skills and intrapersonal skills
c. Required Skill 3: Takes initiative and works well alone and also within a team
Research Data Technician/Specialist - Usds
By TikTok At Mountain View, CA, United States

Responsibilities TikTok is the leading destination for short-form mobile video. Our mission is to inspire creativity and bring joy. TikTok has global offices including Los Angeles, New York, ...

Clinical Research Specialist, (Hybrid, Irvine)- Tmtt
By Edwards Lifesciences At Irvine, CA, United States
Experience in site monitoring/central monitoring skills, site qualification, and site training
Data management experience or analytics
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
Clinical Data Management Specialist
By TalentBurst, an Inc 5000 company At Irvine, CA, United States
Proven track record or validating, testing, and meeting reoccurring deadlines regarding data management.
Position: Analyst, Clinical Data Management
2-4 years of experience required.
Experience with EDC (Electronic Data Capture) systems required.
Good computer skills in Microsoft Office Suite
Good written and verbal communication skills and interpersonal relationship skills
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 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.