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Associate Clinical Site Manager Jobs (NOW HIRING)

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As of Sep 10, 2026, the average hourly pay for associate clinical site manager in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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Infographic showing various Associate Clinical Site Manager job openings in the United States as of July 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Clinical Site Manager

Fort Worth, TX

Artech Information System LLC
Recruiting and Staffing Services • 10K+ employees
Learn more about Artech Information System LLCexternal

Contractor

Re-posted 18 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Successfully implements and executes client s phase I III clinical trials at their assigned sites

Ensures compliance with regulations, guidelines and policies for studies implemented at their assigned sites.

Supports budget and contract negotiation with investigational sites, as applicable, at their assigned sites; ensures payment for services.

Ensure recruitment strategies in place to meet study needs, including patient enrollment targets at their assigned sites.

Collaborates with Clinical Study Teams and within GCSM to identify and resolve site, quality or study execution issues.

Manage existing sites and develops new clinical investigator sites to meet client projected patient recruitment needs in their region. Works with Regional Manager to:

Monitor site quality and performance (metrics); develop solutions to optimize performance.

Monitor site availability, commitments, infrastructure and capabilities.

Ensure all safety issue are communicated and managed by Principal Investigator and study team in timelines appropriate to the regulatory and protocol requirements.

Develop and implements effective corrective action plans for all quality issues identified at assigned sites.

Actively participates with study team to stay current with study needs, communicating as needed with sites within defined timelines.

Train and qualify sites and Principal Investigators.

Develop sites to optimally conduct studies.

Maintain thorough knowledge of country regulations with special focus on regulatory requirements, guidance documents, and standards relating to global clinical trial conduct for medical devices, pharmaceuticals and biologics, and uses that knowledge to enhance site compliance and performance.

Performs all monitoring activities according to protocol monitoring plan and relevant WIs

Maintain / demonstrate knowledge of the protocol, General Monitoring Guidelines (GMG), Protocol

Monitoring Plan (PMP) and all protocol specific requirements

Executes and maintains compliance with all established client processes, procedures, and performance metrics.

With support of Regional Manager, demonstrates flexibility to meet changes in work environment and study milestones with efficiency, and with strong communication and prioritization skills.

Builds positive relationship with principal investigators and site personnel under his responsibility.


Qualifications

Skills:

Microsoft Office proficiency required - Outlook, Excel, Word

Electronic Data Capture (EDC) System Experience required Medidata RAVE preferred

Clinical Trial Management System Experience required - Medidata CTMS preferred

Travel required approximately 60%

Minimum of nine years related experience

Five years of direct regional field clinical monitoring / research.

Currently working in a regional position from an established home office is preferred.

Excellent verbal and written communication, problem solving skills and team orientation.

Education:Medical, pharmaceutical, biology, chemistry degree or RN preferred

For any of these locations below:

North Carolina

South Carolina

Georgia

Florida


Additional Information

Best Regards,

Anuj Mehta

973-967-3402


Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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