Clinical Research Training Specialist 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

• 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

Display strong time management skills, including timely responsiveness to students, sites, and colleagues.

Essential Knowledge, Skills, and Abilities:

60% Director of Training responsibilities and 40% Provision of direct clinical services.

Collaborates with operational and business leadership at this mental health organization to meet fiscal responsibilities and goals for the training programs.

Monitors and reports on all training experiences.

Supports interns in all aspects of their clinical training experiences.

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

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.

Equipment and Computer Software Skills and Abilities:

Gather feedback from trainers and trainees after each educational session

Training Coordinators should have at least 3 years of work experience.

Previous work experience as a Training Coordinator, Training Facilitator, Trainer or a similar role in a corporate environment is preferred.

Bachelor’s degree in healthcare administration, business administration preferred or equivalent experience.

General Duties/Responsibilities (May Include But Are Not Limited To)

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.