Clinical Study Assistant Jobs
By Kelly Science, Engineering, Technology & Telecom At Irvine, CA, United States
Run reports including training matrix reports, metrics for management reviews
Support management of IRB/IEC renewal compliance.
Work with management group to help achieve department goals.
Requires experience and knowledge working with computer systems (Microsoft office –
Assist in payments/tracking for patient reimbursements. Performs data entry in systems
Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
Study Coordinator Jobs
By RootStaff At San Rafael, CA, United States
Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills,
Administrative tasks and activities may be requested by a line manager, study team member, or GSO department staff.
Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival
Activities and responsibilities may include:
The SS I is not allocated as a resource to any specific study or program.
BOARD Quarterly MVR GSO Compliance and other metrics
Part-Time Contract Clinical Study Coordinator
By NeuroPace At San Francisco Bay Area, United States
General understanding of clinical documentation management and document control
Manage the eTMF (Trial Master File) system
Minimum of 2 years relevant work experience
Medidata and eTMF experience preferred
Previous experience in a clinical or regulatory department highly preferred.
Proficient in MS Word, Excel and Adobe PDF. Experience with clinical trial software systems, including eTMF, preferable
Clinical Study Coordinator (Remote)
By Guardant Health At Palo Alto, CA, United States
Facilitate the coordination and management of clinical studies
Knowledge of ICH/GCP guidelines, including basic understanding of regulatory requirements in other countries, preferred
A minimum of 1 year experience in a CLIA, CAP-accredited laboratory preferred
A minimum of 1 year of experience as a clinical research coordinator preferred, ideally in a lab or device setting
Working knowledge of local, state, and federal laboratory regulations
Effective interpersonal skills and ability to effectively communicate (verbal and written) across all levels of the company
Clinical Program Nurse Coordinator Iii
By Sutter Health At , San Francisco, Ca $80.50 - $106.26 an hour
Equivalent experience will be accepted in lieu of the required degree or diploma.
DEPARTMENT SPECIFIC CERTIFICATION & LICENSURE
Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.