Hybrid Project Administrator - Medical Writing & Trials

Technical Resources International, Inc.; Bethesda, Northern (MD, KY); Hybrid; USD 57,000 - 65,000; Full time

Job summary

Technical Resources International, Inc. is seeking a Project Administrator to support clinical trials from Bethesda, MD. The role blends project management tasks with document editing and reporting, requiring solid communication and meticulous data handling.

The position is full-time in a hybrid setup with 2 days in the Bethesda office and 3 days remote. A Bachelor’s degree and clinical research exposure are preferred for this role.

Qualifications

• Bachelor's degree required.
• Strong written and verbal communication skills.
• Experience in clinical research preferred.
• Detail-oriented with ability to multitask and meet deadlines.

Responsibilities

• Assist on project management activities and produce reports.
• Generate level of effort reports and monitor project status.
• Draft and submit project progress reports.
• Coordinate conference calls and distribute meeting minutes.
• Prepare, revise, and reconcile SOPs and project plans within timelines.
• Assist with QA audit findings resolution.
• Maintain data in project tracking systems.
• Provide ad hoc support as needed.

Skills

Communication skills

Interpersonal skills

Attention to detail

Multitasking

Flexibility

FDA guidelines knowledge

Education

Bachelor's Degree

Tools

Microsoft Office

Clinical trial databases

AI tools

Job description

Technical Resources International, Inc. is seeking a Project Administrator to support clinical trials from Bethesda, MD. The role blends project management tasks with document editing and reporting, requiring solid communication and meticulous data handling.

The position is full-time in a hybrid setup with 2 days in the Bethesda office and 3 days remote. A Bachelor’s degree and clinical research exposure are preferred for this role.