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Clinical Study Manager Jobs in Texas (NOW HIRING)

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Required Experience * 2+ years of global study management experience * Experience across multiple countries/regions * Phase I-III clinical trials experience (Phase III required) * Oncology experience ...

DM Clinical

Study Manager I (4011)

Sugar Land, TX · On-site

A Study Manager I is responsible to ensure that quality research is conducted at assigned ... Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator ...

Clinical Research Solution LLC

Be Seen First

Clinical Study Coordinator

Houston, TX · On-site

$49K - $59K/yr

Position Summary The Clinical Research Coordinator will support daily clinical trial operations ... Manage investigational product accountability * Communicate with sponsors/CROs regarding queries ...

DiaSorin

Clinical Study Coordinator

Austin, TX · On-site

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Excellent communication, organizational and time management skills * Proficiency with Microsoft ...

DiaSorin

Clinical Study Coordinator

Austin, TX · On-site

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Excellent communication, organizational and time management skills * Proficiency with Microsoft ...

SGS

Clinical Study Project Manager

Richardson, TX · On-site

... data management), study/project execution, data analysis and clinical study report/other deliverables, and archiving. During study/project execution, the Study Project Manager tracks project ...

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How much do clinical study manager jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for clinical study manager in Texas is $58.24, according to ZipRecruiter salary data. Most workers in this role earn between $47.26 and $65.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Texas?

The most popular types of Clinical Study jobs in Texas are:

What are popular job titles related to Clinical Study Manager jobs in Texas?

For Clinical Study Manager jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Texas look for?

The top searched job categories for Clinical Study Manager jobs in Texas are:

What cities in Texas are hiring for Clinical Study Manager jobs?

Cities in Texas with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Texas as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, 2% Contract, and 1% Nights. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $121,147 per year, or $58.2 per hour.

Clinical Study Manager

Plano, TX • On-site

Argon Medical Devices Inc
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

6.5

Company rating: 6.5 out of 10

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Learn more about Argon Medical Devices Incexternal

Full-time

Posted 12 days ago

Job description

Company Overview:
Argon Medical Devices is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon's brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.
Position Overview:
The Clinical Study Manager (CSM) is responsible for the planning, execution, and oversight of clinical investigations for medical devices across the product lifecycle, including pre-market and post-market studies. The CSM ensures that clinical studies are conducted in compliance with applicable regulatory requirements, including ISO 14155, FDA regulations, EU MDR, and Good Clinical Practice (GCP).
This role serves as the operational lead for assigned studies and as a primary point of contact for study timelines, budgets, site performance, vendors, and data integrity. The CSM collaborates closely with cross-functional partners including Regulatory Affairs, Quality, Medical Affairs, and Product Development to generate high-quality clinical evidence that supports product safety, performance, and regulatory objectives.
What you will do:
Study Planning & Execution
  • Lead the planning, design, and execution of clinical studies (IDE, post-market, PMCF, registries, and observational studies) in alignment with business and regulatory strategy.
  • Manages and oversee all aspects of clinical research projects.
  • Ensure projects are timely, are evaluating accurate data, and are producing precise results.
  • Plans, directs, creates, and communicates the study timeline.
  • Develops detailed project plans, and monitors project milestones against performance indicators.
  • Ensures the project is planned and conducted in accordance with all applicable regulations, standard operating procedures, and good clinical practices (GCP).
  • Manages risk assessment and mitigation.
  • Generates reports to provide periodic status updates.
  • Develop, review, and manage clinical study documentation, including protocols, informed consent forms, case report forms (CRFs), statistical plans (as applicable), and clinical trial agreements.
  • Serve as the primary operational lead for assigned studies from site selection through study closeout.

Site Management
  • Coordinate site feasibility, selection, qualification, initiation, monitoring, and close-out activities.
  • Provide oversight of site performance, enrollment, data quality, and protocol compliance.
  • Support training and ongoing communication with investigators and site staff

Regulatory & Compliance
  • Ensure clinical investigations are conducted in accordance with ISO 14155, FDA regulations, EU MDR, and applicable international GCP requirements.
  • Support regulatory submissions, audits, and inspections by maintaining inspection-ready Trial Master Files (TMF) and related clinical documentation.
  • Collaborate with Regulatory Affairs to ensure alignment between study design, clinical evidence generation, and regulatory strategy.

Vendor & Budget Oversight
  • Manage and oversee clinical research organizations (CROs), laboratories, and other vendors to ensure delivery of contracted services.
  • Develop and manage study budgets, forecasts, and resource plans; monitor expenditures against approved budgets.
  • Identify and mitigate operational, timeline, and budgetary risks.

Data & Project Management
  • Track study milestones, timelines, and deliverables using clinical trial management tools.
  • Monitor data quality and completeness; coordinate resolution of data queries and issues.
  • Ensure accurate, timely reporting of study status, risks, and results to internal stakeholders.

Team Leadership & Collaboration
  • Provide guidance, training, and operational oversight to Clinical Research Associates (CRAs) and other study team members, as applicable.
  • Provide guidance, training, and operational oversight to Clinical Research Associates (CRAs) and other study team members, as applicable

Contribute to continuous improvement of clinical operations processes, procedures, and best
Skills for Success:
Required education and experience
  • Bachelor's degree in Life Sciences, Engineering, or a related field required.
  • Master's degree or PhD preferred.
  • 3-8+ years of experience in clinical research, with a minimum of 2+ years in medical device study management.
  • Demonstrated experience managing pre-market and/or post-market medical device clinical studies.
  • Hands-on experience with site start-up, enrollment management, monitoring oversight, and CRO management.

Preferred Education and experience
  • Certification through a professional organization such as ACRP or SOCRA.
  • Experience working with interventional or procedural studies (IR, vascular, cardiology preferred)

Knowledge & Technical Skills
  • Strong knowledge of ISO 14155, FDA regulations, EU MDR, and GCP.
  • Proficiency with Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and electronic Trial Master Files (eTMF).
  • Working knowledge of medical device quality systems and clinical documentation requirements

Core Competencies
  • Strong project management, organizational, and risk-management skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a fast-paced, cross-functional environment.
  • Demonstrated leadership and problem-solving capabilities.

Physical demands & Travel required
  • Ability to travel to clinical sites and industry meetings as required (up to 40%).

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