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Senior Clinical Research Associate Jobs in Spring, TX

MD Anderson

Sr Clinical Dietitian

Houston, TX · On-site

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Senior Clinical Dietitian plays a vital role in advancing ...

MD Anderson

Sr Clinical Dietitian

Houston, TX · On-site

$77K/mo

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Senior Clinical Dietitian plays a vital role in advancing ...

MD Anderson Center

Sr Clinical Dietitian

Houston, TX · On-site

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Senior Clinical Dietitian plays a vital role in advancing ...

MD Anderson Center

Sr Clinical Dietitian

Houston, TX · On-site

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Senior Clinical Dietitian plays a vital role in advancing ...

MD Anderson

Sr Clinical Dietitian

Houston, TX · On-site

The University of Texas MD Anderson Cancer Center is a leading institution focused on cancer care, research, education, and prevention. The Senior Clinical Dietitian plays a vital role in advancing ...

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All JobsClinical Research Associate JobsSenior Clinical Research Associate JobsSenior Clinical Research Associate Jobs in Spring, TX

Senior Clinical Research Associate information

See Spring, TX salary details

$32K

$83.9K

$127.7K

How much do senior clinical research associate jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior clinical research associate in Spring, TX is $83,929.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,600.00 and $113,900.00 per year, depending on experience, location, and employer.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

What are the key skills and qualifications needed to thrive as a senior clinical research associate, and why are they important?

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
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Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research Associate job openings in Spring, TX as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $83,929 per year, or $40.4 per hour.

Unblinded Clinical Research Coordinator II (4015)

Dm Clinical Research Group

Houston, TX • On-site

$55 - $75/hr

Other

Re-posted 9 days ago

Job description

Job Details

Job Location: CyFair - Houston, TX 77065DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Pharmacy Technicians, LPN's and CMA's are encouraged to apply!


Duties & Responsibilities

  • Compound and dispense prescribed IP as needed by Sponsor approved protocol

  • Study IP management

  • Provide training and guidance for new team members

  • Assist in all aspects of company start up activities as required

  • Supervise and maintain records of all medications

  • Ensure compliance with study-specific blinding plans

  • Perform regular audits on the clinical data to assess percent completeness and accuracy

  • Assist in onboarding training for new members

  • Ensure external sites’ regulatory documents and required site certifications are up to date

  • Provide consultative support regarding the preparation and dosing of drugs

  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction

  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials

  • Understand and apply all applicable site procedures

  • Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting

  • Develop operating procedures, guides and best practices for data entry portals and project workflows

  • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.

  • Any other duties or tasks assigned by the manager


Knowledge & Experience

Education:



  • Associates Degree required or 2 years of formal educational coursework

  • Bachelor's degree, preferred

  • Secondary or Foreign Medical Graduate, preferred


Experience:



  • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required

  • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required

  • 1+ year utilizing CRIO, preferred


Credentials:



  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred

  • Pharmacy Technician Certification, preferred

  • Completion of DMCR-required training, including GCP, OSHA and IATA


Knowledge and Skills:



  • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.

  • Excellent communication and customer service skills, both written and verbal

  • Excellent time-management skills

  • Ability to remain composed under pressure and high-stress situations

  • Outgoing personality

  • Well-organized with attention to detail.

  • Must be able to multitask.

  • Bilingual (Spanish) preferred


Qualifications
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