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Clinical Monitoring Jobs in Texas (NOW HIRING)

Pharmacist PRN

Sherman, TX · On-site

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

Pharmacist -PRN

Sherman, TX · On-site

$52 - $62.50/hr

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely ...

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Clinical Monitoring: Continuously monitor patients during hyperbaric sessions, assess vital signs, and respond immediately to any changes in condition or adverse events. * EMR Documentation: Complete ...

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

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

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 21-40

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.

$52 - $62.50/hr

Other

Re-posted 10 days ago


Job description

The Pharmacist is responsible for the review and interpretation of physician orders, the dispensing of medications, the clinical monitoring of drug therapies and the provision of accurate and timely drug information while complying with all legal and practice standards. In the absence of the Director of Pharmacy, the Pharmacist may be required to assume the essential responsibilities and perform the duties of the Director.

EDUCATION, EXPERIENCE, TRAINING

1. Current pharmacist license from the Texas Board of Pharmacy.
2. Graduate from an accredited College of Pharmacy
3. Sterile IV Preparation Certification as described in the Texas State Board of Pharmacy Laws, Rules, and Regulations.

1. Prepares and dispenses medications, including sterile, chemotherapy, and parenteral nutrition preparations safely and accurately using appropriate techniques.
2. Assists with pharmacokinetics consult service and drug dosing per Hospital policies/protocols.
3. Reviews/interprets culture and susceptibility data for antibiotic appropriateness and recommends changes, as needed.
4. Reads, extracts, and interprets information in patient charts accurately.
5. Detects and reports suspected adverse drug reactions and medication errors accurately and in a timely manner.
6. Sustains the formulary by minimizing non-formulary procurements, utilizing therapeutic substitution protocols, and promoting rational medication therapy selection.
7 Provides clinical consultation and clarification to practitioners. Recommends evidence based medication therapy regimens and monitoring plans. Suggests appropriate cost effective therapeutic alternatives to medical staff, as needed.
8. Provides accurate, adequate and timely drug information to the professional staff.
9. Provides drug information to patients and families, as needed.
10. Documents all clinical activities and interventions accurately and completely.
11. Supervises and directs pharmacy support personnel. Verifies the daily activities of the pharmacy technicians.
12. Completes and documents inspections of all assigned medication storage areas. Identifies and replaces outdated and unusable medications.
13. Ability to communicate effectively (orally and in writing).
14. Maintains regular attendance.
15. Performs other duties as assigned or required.