Technical Documentation Specialist
Job Description
R&D Partners is seeking to hire a Technical Documentation Specialist II in Fort Worth, TX.
Your main responsibilities as a Technical Documentation Specialist II:
Coordinate collection and processes essential trial documents between investigator sites and company 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.
What we are looking for in a Technical Documentation Specialist II:
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
Why Choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including:
- Medical insurance PPO, HMO & HSA
- Dental & Vision insurance
- 401k plan
- Employee Assistance Program
- Long-term disability
- Weekly payroll
- Expense reimbursement
- Online timecard approval
Pay Scale:
$78,728 $86,171 (Dependent on Experience)
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.