Top 6 In house cra Jobs in Washington, Dc

In-House Clinical Research Associate
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
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
Sr. In-House CRA
Emmes Group —Rockville, MD
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Organizational skills
- Health insurance
- 401(k)
2d
MedTech Site Manager 1
IQVIA —Washington, DC
- $74,500 - $124,100 a year
- Full-time
- Remote
- Bachelor of Science
- Mid-level
- Team management
- Work from home
2d
Associate Director, Clinical Operations
Technical Resources International, Inc. —Bethesda, MD
- $130,000 - $175,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Data analysis skills
12d
Associate Director, Clinical Operations
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Microsoft Word
- Microsoft Excel
- Data analysis skills
11d

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Associate Account Manager - Clinical Trial Division - West Coast, US
Thermo Fisher Scientific —Washington, DC
Leverage business intelligence platforms and internal digital tools to identify and advance new business opportunities.
$76,700 - $115,025 a year
11d
Clinical Research Associate
Georgetown University —Washington, DC
Must have a Bachelor's degree and 5+ years of experience or equivalent relevant work experience; Master’s Degree in a related field is a plus.
$47,586.00 - $87,558.13 a year

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In-House Clinical Research Associate

TECHNICAL RESOURCES INT'L
Bethesda, MD

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Job Details

Full-time

Qualifications

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

Full Job Description

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.

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in house cra jobs in washington, dc

In-House Clinical Research Associate

In-House Clinical Research Associate

Sr. In-House CRA

MedTech Site Manager 1

Associate Director, Clinical Operations

Associate Director, Clinical Operations

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