Clinical Research Specialist I Jobs in California

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

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

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.

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.

• 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

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).

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

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.

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).

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.

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

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.

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

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

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).

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.

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).

1 year of Clinical research related experience

Schedules patients for research visits and procedures.

Maintains accurate source documents related to all research procedures.

Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.

Schedules and participates in monitoring and auditing activities.