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Clinical Monitoring Jobs in Texas (NOW HIRING)

Join Us in Shaping the Future of Clinical Research   Adams Clinical is a leading clinical trial ... These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and ...

Clinical Research Assistant

Dallas, TX · On-site

$19.23 - $23.08/hr

Support CRCs during monitoring visits and assist with preparing documentation and materials to ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...

Showing results 41-60

Clinical Monitoring information

See Texas salary details

$11

$38

$64

How much do clinical monitoring jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical monitoring in Texas is $38.31, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $49.04 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical monitoring, and why are they important?

To thrive in Clinical Monitoring, you need a solid background in life sciences or nursing, strong knowledge of clinical trial protocols, and often a relevant degree such as a BS in a scientific field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Exceptional attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing trial sites and ensuring compliance. These competencies are vital for ensuring data integrity, regulatory adherence, and the smooth progress of clinical trials.

What is the difference between Clinical Monitoring vs Clinical Data Management?

AspectClinical MonitoringClinical Data Management
Primary RoleOversees site activities, ensures protocol adherence, monitors patient safetyCollects, validates, and manages clinical trial data
Required CredentialsTypically a degree in life sciences, nursing, or related field; often requires monitoring certificationsDegree in life sciences, biostatistics, or related; data management certifications beneficial
Work EnvironmentOn-site at clinical trial sites or remotely, interacting with site staffPrimarily office-based, working with electronic data capture systems
Industry UsageCommonly used in clinical trial phases, especially during site visitsUsed throughout the trial for data collection, cleaning, and analysis

Clinical Monitoring focuses on overseeing clinical trial sites and ensuring compliance, while Clinical Data Management handles the collection and validation of trial data. Both roles are essential in clinical research, often working closely but with distinct responsibilities.

What is clinical monitoring?

Clinical monitoring is the process of overseeing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures, Good Clinical Practice (GCP), and regulatory requirements. Clinical monitors, often called Clinical Research Associates (CRAs), are responsible for checking the progress of a clinical trial at research sites, verifying data accuracy, ensuring participant safety, and ensuring compliance with regulations. Their work is essential in maintaining the integrity of clinical data and the safety of trial participants.

What are some common challenges faced by professionals in clinical monitoring, and how can they be addressed?

Clinical Monitoring professionals often encounter challenges such as managing multiple study sites, ensuring protocol compliance, and maintaining clear communication with site staff. Navigating regulatory requirements and handling unexpected issues, like protocol deviations or data discrepancies, can also be demanding. To address these, strong organizational skills, proactive communication, and thorough documentation are essential. Building collaborative relationships with site personnel and staying updated on regulatory guidelines can help ensure smoother study progress and data integrity.
What are the most commonly searched types of Clinical Monitoring jobs in Texas? The most popular types of Clinical Monitoring jobs in Texas are:
What cities in Texas are hiring for Clinical Monitoring jobs? Cities in Texas with the most Clinical Monitoring job openings:
Infographic showing various Clinical Monitoring job openings in Texas as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $79,695 per year, or $38.3 per hour.

Lead Dosing Session Monitor

Adams Clinical

Dallas, TX • On-site

$60 - $70/hr

Per diem

Posted 19 days ago


Job description

Join Us in Shaping the Future of Clinical Research

Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. 

At Adams Clinical, you'll find: 

  • A culture of respect, transparency, and continuous improvement 
  • Opportunities for professional growth and learning 
  • A team dedicated to improving lives through innovation and integrity 

If you're passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we'd love to have you on our team. 

Job Role

Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions.

We are seeking a per diem Psychedelic Dosing Monitor/Therapist for exciting clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or more of our research site locations. Willingness to travel between regional sites is a plus but not required (Watertown and Boston; Harlem and Bronx).

Key Responsibilities

  • Serve as Lead Study Therapist in psychedelic clinical trials for depression, anxiety, and other mood disorders. 
  • Complete study-sponsored therapist training, and Adams Clinical site-specific training requirements. 
  • Provide support to participants throughout the clinical trial in alignment with the study protocol and training guidelines. 
  • Collaborate with clinicians and site staff managing participant participation in the study. 

Qualifications

  • Licensed mental health professional in Massachusetts, New York, Pennsylvania, or Texas (e.g., PsyD, PhD, LCSW, LMSW, LMHC, LMFT), with the ability to provide psychotherapy in compliance with state regulations  
  • Attention to detail is critical for this role to ensure accurate observation, documentation, and reporting of dosing sessions, with strict adherence to ICH-GCP standards and protocol requirements. 
  • Experience working with individuals with depression, anxiety, or other mood disorders  
  • Strong interpersonal and communication skills, with an interest in advancing mental health care in a clinical research setting. 
  • Ability to meet fixed scheduling expectations, including consistent on-site availability.  
  • Final candidate must be approved by both Adams Clinical and the study sponsor.  

Commitments

  • This is a per diem, as-needed position, with work hours based on study enrollment, participant availability, and trial timelines.
  • Therapists should anticipate approximately 2-3 days per week of direct participant-facing responsibilities. These include pre-dose preparation, real-time monitoring during psychedelic dosing sessions, and post-dose follow up sessions. The exact schedule will vary based on study volume, participant availability, and internal scheduling priorities.
  • Flexibility and responsiveness to shifting scheduling needs are essential.
  • A majority of the participant appointments must be conducted in person at our research site locations, and a portion can be conducted remotely by the therapist
  • Therapists must be willing to learn and adhere to ICH-GCP standards.
  • Additional responsibilities include administrative tasks, onboard, and study-related training, as well as other tasks assigned.

Pay: $60.00 - $70.00 per hour

Benefits:

  • 401(k) / 401(k) matching

Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.

In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.