ZipRecruiter

Log In

1

Clinical Study Associate Jobs in Dallas, TX (NOW HIRING)

SGS

Clinical Research Coordinator I

Richardson, TX · On-site

$22 - $29/hr

... abiding by Good Clinical Practice (GCP) guidelines. JOB FUNCTIONS * Performs station and ... Arrange work for studies Qualifications EDUCATION AND EXPERIENCE * Associate degree or 2 years ...

previous pagenext page

Showing results 21-40

All JobsClinical Study Associate JobsClinical Study Associate Jobs in Dallas, TX

Clinical Study Associate information

See Dallas, TX salary details

$12

$31

$54

How much do clinical study associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical study associate in Dallas, TX is $31.20, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $41.15 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Study jobs in Dallas, TX?

The most popular types of Clinical Study jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Clinical Study Associate jobs?

Cities near Dallas, TX with the most Clinical Study Associate job openings:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Dallas, TX as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $64,897 per year, or $31.2 per hour.

Clinical Research Coordinator II

ALLIANCE CLINICAL LLC

Lewisville, TX • On-site

$60 - $80/hr

Other

Posted 17 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Coordinator II

FullTime Technical Alliance Clinical Lewisville, Lewisville, TX, US

Summary:

The Clinical Research Coordinator II (CRC II) supports daily clinical research operations under the direction and ongoing supervision of the Site Manager, Site Director, and Principal Investigator, in accordance with required protocols. The CRC II is responsible for coordinating and managing clinical trials designed to test the effectiveness of new drugs or biotechnology across Phases I-IV.

Essential Duties and Responsibilities:
  • Communicate effectively and courteously with study participants regarding study objectives and ongoing instructions.
  • Acknowledge study patients' needs and tend to them appropriately.
  • Collect participant medical history and medical conditions.
  • Obtain informed consent in accordance with regulatory and protocol requirements.
  • Maintain study drug dispensation and accountability records.
  • Coordinate with laboratories to ensure timely participant testing.
  • Collect and review concomitant medication information.
  • Collect and review medical records for protocol and regulatory compliance.
  • Conduct adverse event (AE) and serious adverse event (SAE) assessments.
  • Perform EKGs, vital signs, nasal swabs, and protocol-specific procedures.
  • Manage and oversee clinical laboratory reports.
  • Maintain site regulatory files in accordance with SOPs and regulations.
  • Verify the accuracy and completeness of data collected.
  • Assist with the recruitment and engagement of study participants as needed.
  • Document temperatures for investigational product (IP) stored on‑site.
  • Develop study eSource documents in compliance with study protocols.
  • Manage and lead multiple clinical trials across different therapeutic areas.
  • Manage all required study start‑up documentation, training, and timelines for assigned protocols.
  • Meet all study protocol requirements and deadlines.
  • Manage and adhere to approved study budgets.
  • Participate in and support interim monitoring visits (IMVs) and site initiation visits.
  • Support sponsor audits and regulatory inspections.
  • Perform Quality Control (QC) and compliance reviews within study trials.
  • Adhere to site SOPs, Good Clinical Practice (GCP), and regulatory requirements.
  • Strictly adhere to confidentiality and compliance standards.
  • Perform other duties as assigned.
Qualifications:
  • Associate’s degree in healthcare or related field preferred.
  • Minimum of 4 years of experience in Clinical Research and knowledge of protocols and procedures required.
  • Minimum of 4 years of experience in FDA regulations and GCP.
  • Minimum of 2 years of experience in phlebotomy and EKGs required.
  • Proven track record of analytical reasoning skills.
  • Exceptional attention to detail and organizational skills.
  • Must possess excellent verbal and written communication skills.
  • Excellent customer service skills with internal and external stakeholders.
  • A proven ability to multitask in a rapidly changing environment.
Certificates, Licenses, and Registrations:
  • CPR certification required.
  • Maintain IATA certification and any other required job‑related certifications.
  • Good Clinical Practice (GCP) certification required.
  • Current, active certification as a Medical Assistant required.

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H-1B, TN, or STEM OPT training plans) are not eligible for this role.

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.

#J-18808-Ljbffr

Apply