TalentBurst | Professional - Miscellaneous - Technical Documentation Specialist II TX | fort worth, tx - TalentBurst
fort worth, TX 76102
About the Job
Job Title: Technical Documentation Specialist II
Location: Ft Worth, TX
Duration: 24 Months
Job Description:
Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions.
Ensure accuracy and quality of site documents included in the site initiation packets and throughout the duration of the study.
Enter and maintain site information and document tracking in current clinical trial management systems.
Ensure trial documentation is well organized, available, current, and archived in a timely manner in the sponsor Trial Master File and ensure audit readiness.
Follow applicable work processes, SOPs, communication plans, etc.
Ensure timely elevation of issues with sites related to preparation/collection of trial documents, initiation packets, site budget and contracts, or other relevant documentation.
May interact with and advise other functions on CTDM responsibilities. Interactions include but are not limited to Global Clinical Site Development, Clinical Trial Lead, Clinical Site Managers, etc.
May provide support before and during audits, both internal and external when applicable.
Self-starter
Customer Focus
Action Oriented
Communicates Effectively
Collaborates
Preferred Qualifications:
Bachelor's degree in life sciences (Medical, pharmaceutical, biology, chemistry degree or RN)
*2 years related experience (e.g., business administration)
1 year clinical trial experience (e.g., ophthalmology, study coordinator, etc.)
Proficient in Microsoft Office to include Word, Excel, PowerPoint
Excellent verbal and written communication skills
Excellent organization skills with exceptional attention to detail
History of working with multiple internal and external customers
#TB_PH
Location: Ft Worth, TX
Duration: 24 Months
Job Description:
Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions.
Preferred Qualifications:
*2 years related experience (e.g., business administration)
#TB_PH
Source : TalentBurst