Clinical Trial Management System Designer

Job overview

The Clinical Trial Management System Designer works onsite in San Antonio, TX, in an office, laboratory, or clinical environment. Compensation is not specified. The role supports Pinnacle Clinical Research’s eSource and data-management work across multiple research sites.

What you'll do

• Create and manage eSource for document capture in the site’s CRIO clinical trial management system
• oversee CTMS functions related to eSource and data management
• coordinate with site staff and external personnel
• manage multiple projects and deadlines across locations
• maintain eSource integrity and version control
• secure accurate documents and remove obsolete versions
• lead applicable eSource meetings
• and ensure staff approvals before documents are published. Occasional domestic or international travel may be required.

What we're looking for

Skills & competencies

clinical trial management system

esource

clinical research

crio

data management

document control

gcp

ich

hipaa

fda requirements

san antonio tx

pinnacle clinical research

Work arrangement

• Weekend coverage required

Benefits & perks

• 401(k), medical, dental, vision, short- and long-term disability, FSA, life insurance, three weeks of paid time off, and 14 paid company holidays.

Why this role

The posting requires knowledge of clinical research regulations, CITI and GCP training certification, and familiarity with clinical trial management systems; an associate degree in a scientific field or equivalent is required.

About the employer

Pinnacle Clinical Research is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.