Skip to content

Job Title, Skills or Company

City, State, ZIP or "Remote"

Sort by

RelevanceDate

Distance

Job Type

Minimum Salary

Date Added

Refine Your Search

Sort by

Relevance
Date

Job Type

All Job Types
Full-time

Minimum Salary

All Salaries
$65,000
$75,000
$85,000
$100,000

Date Added

Anytime
24 hours
7 days
14 days
30 days

7

Technical Resources International jobs

In-House Clinical Research Associate
Technical Resources International, Inc. —Bethesda, MD
- $50,000 - $80,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
Quality Assurance Specialist
Technical Resources International, Inc. —Bethesda, MD
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
Medical Writer
Technical Resources International, Inc. —Bethesda, MD
- $70,000 - $85,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Master's degree
S & P Associate
Technical Resources International, Inc. —Bethesda, MD
- $54,000 - $60,000 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Customer service
- Bachelor of Science
13d
Central Monitor
Technical Resources International, Inc. —Bethesda, MD
- $85,000 - $115,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Continuous improvement
Regulatory Specialist
Technical Resources International, Inc. —Bethesda, MD
- $70,000 - $85,000 a year
- Full-time
- Hybrid work
- Background check
- Current TB test
- Mid-level
Quick Apply
S & P Specialist
Technical Resources International, Inc. —Bethesda, MD
- $70,000 - $85,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Master's degree

More jobs to discover

Find similar jobs that you might be interested in.

Call Center Quality Assurance & Training Specialist
Imagine Pediatrics —Remote
Listen to recorded calls and assess the quality of interactions based on predetermined criteria, including adherence to scripts, professionalism, accuracy of…
$65,000 - $85,000 a year
Quick Apply
Commissioning & Quality Assurance Specialist - Commercial HVAC
Optimal Air Solutions —Tomball, TX
Valid driver's license with an insurable driving record. He/she will also have high critical thinking skills and be able to solve issues in the field.
From $30 an hour
Quick Apply
6d

Show more similar jobs

1

I want to receive the latest job alert for Technical Resources International

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

Technical Resources International jobs near

Quality Assurance Specialist jobs in Bethesda, MD

Clinical Research Associate jobs in Bethesda, MD

Medical Writer jobs in Bethesda, MD

Regulatory Specialist jobs in Bethesda, MD

Monitor jobs in Bethesda, MD

Quality Assurance Specialist jobs in Phoenix, AZ

Quality Assurance Specialist jobs in Frederick, MD

Quality Assurance Specialist jobs in New Jersey

Quality Assurance Specialist jobs in Raleigh, NC

Family Support Specialist jobs in Texas

Quality Assurance jobs in Denver, CO

Quality Control Chemist jobs in Chicago, IL

Clinical Research Associate jobs in Richmond, VA

Clinical Research Associate jobs in Colorado

Clinical Research Associate jobs in Orlando, FL

Clinical Research jobs in Virginia

Clinical Research Associate jobs in Morgantown, WV

Patient Service Associate jobs in Philadelphia, PA

Nursing Clinical Instructor jobs in St. Louis, MO

Medical Courier jobs in Methuen, MA

In-House Clinical Research Associate

Technical Resources International, Inc. -
Bethesda, MD

Apply Now

Job Details

Full-time
$50,000 - $80,000 a year

Qualifications

Microsoft Excel
Microsoft Outlook
Phone communication
Writing skills
Word embeddings
Medical terminology

Full Job Description

Location

Bethesda, MD 20817 US (Primary)

Category

Clinical Operations

Job Type

Full-Time

Salary Range

50,000-80,000

Education

Bachelor's Degree

Travel

None

Job Description

The In-House Clinical Research Associate is responsible for supporting clinical study teams, primarily the field CRAs and the Project/Task Manager, as required on clinical trial administrative duties. Duties may include but are not limited to:

Retrieve, file, and maintain essential regulatory documents from clinical trial sites for the Trial Master File (TMF) or another central documents file platform or system held by TRI or Sponsor/Client.
Review site essential regulatory documents for accuracy and completeness as required by FDA regulations, ICH GCP, Sponsor requirements, and corporate or Sponsor SOPs.
Track essential regulatory documents in a centralized web-based system and/or other database.
Troubleshoot essential regulatory document issues by applying existing knowledge to solve new problems.
Coordinate or assist in distribution of trial-related materials to study sites.
May assist in monitoring visit preparation and/or follow up such as teleconference arrangements, regulatory file review, and agenda preparation.

NOTE: Specialized experience in eTMF (e.g., Veeva Vault) processing and system administration skills-sets and/or additional responsibilities may be required for some staff. This job may serve as a transition or training role for the position of field CRA, as appropriate.

Job Requirements

Understanding of medical and clinical trials terminology.
Ability to negotiate with investigators, research nurses, and site staff to reach desired resolution.
Able to work independently or with minimal supervision as well as within a team.
Excellent attention to detail with organizational and prioritization skills for efficient productivity.
Proficiency with Microsoft Office is required (MS Word, Excel, Outlook at a minimum).
Excellent professional writing and verbal communication skills (position requires clear phone and email communication).
Able to multi-task during the review/processing and preparation of essential regulatory documentation.
Must be self-motivated, with a positive attitude, and willing to ask questions to get the job done right.
Must have excellent time management skills, able to adhere to strict timelines and expectations.
Experience with regulatory document review/collection and IRB submissions (including OHRP regulations), a plus.
Experience with using a Trial Master File, a plus.
This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.

Apply Now

Job Seeker Tools

Salary Estimator
Glassdoor Community

Country

Employer Tools

Post Jobs

Browse

All Jobs
All Salaries
All Cities
All Companies

Stay Connected

Contact Us

Job Seeker Tools

Salary Estimator
Glassdoor Community

Country

Employer Tools

Post Jobs

Browse

All Jobs
All Salaries
All Cities
All Companies

Stay Connected

Contact Us

Country

Take your job search wherever you go.

© 2026 SH Inc. SimplyHired is part of the Indeed Site, and by using SimplyHired you agree to the Indeed Terms of Service.

Privacy
Terms
Cookies
Privacy Center
Accessibility
Your Privacy Choices