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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

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 ...

DM Clinical

Study Manager I (4012)

Houston, 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 ...

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How much do clinical study manager jobs pay per hour?

As of Aug 25, 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.

Associate Clinical Study Manager

San Antonio, TX • On-site

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

Other

Posted 5 days ago

Job description

What the Associate Clinical Study Manager does at Worldwide


The Associate, Clinical Study Manager will be responsible for the site-level monitoring activities of on one or more allocated Phase I through IV Clinical Trials that may be local, regional, or global in scope. Supports the CSM with directing the technical, financial, and operational aspects to ensure the successful completion of the clinical trials. Works with functional area leads to identify and evaluate essential project prerequisites. The ACSM cooperates with the CSM to ensure all project deliverables meet client’s time/quality/cost expectations.


What you will do


  • Coordinate study monitoring visits, to include (but not limited to): ensuring the monitor has access to the relevant electronic systems, reserving monitoring space, assembling study documents for CRA review, and ensuring all follow-up action items are completed in a timely manner.
  • Work collaboratively with other clinic departments to ensure all queries are answered in a timely manner.
  • Manage and store signed approval forms for Clinical Lab, PK processing, Clinspark Go live, and Clinspark training and access request forms from clients.
  • Coordinate and collate signature forms for SIV attendance, logistics meetings, and any other protocol training related meetings, file in the appropriate study folder.
  • Ensure staff training is documented in the appropriate study files on the study protocol and other related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations.
  • Facilitate shipment of samples to bioanalytical labs for analysis per the study timeline and/or client request.


What you will bring to the role


  • Excellent communication, planning, and organizational skills.
  • Sense of urgency and ability to be adaptable in a fast-paced and rapidly changing environment.
  • Self-motivated and excellent problem-solving skills.
  • Ability to work independently.
  • Ability to negotiate and liaise with clients in a professional manner.
  • Must have satisfactory customer service skills.


Your experience


  • Bachelor’s Degree (Life Sciences or Health preferred) or 4 years clinical research experience Or Associates Degree with 2 years clinical research experience.
  • Min 1 year as a Clinical Research Coordinator preferred


Apply