Adams ClinicalVerified Source

Clinical Research Assistant, Entry Level at Adams Clinical (Dallas)

40K–48K
Onsite · Dallas, Texas
Posted August 14, 2026
full-time

Overview

Join a mission-driven clinical trial network focused on late phase studies for psychiatric and neurological conditions. You will support site operations, data collection, and regulatory compliance under supervision, contributing to high-quality trial execution at the Dallas site. This entry point role offers hands-on exposure to ICH-GCP, source documentation, EDC data entry, and participant coordination. You will work with a team dedicated to data integrity, participant safety, and continuous improvement.

What You'll Do10

  • 1Build and support study start-up activities including supply inventory and site readiness to enable smooth first-visit operations
  • 2Assist with participant screening workflows and scheduling to support eligibility assessments
  • 3Schedule and prepare for participant visits with source prep, lab kits, and CRFs
  • 4Serve as a participant liaison to confirm appointments, coordinate transportation, and maintain ongoing communication
  • 5Escort participants during on-site visits and assist with vital signs ECGs and specimen collection as trained
  • 6Complete ALCOA+-compliant source documentation for delegated procedures
  • 7Enter data into EDC systems and assist with query resolution
  • 8Maintain study binders, charts, and logs and support supply management
  • 9Ensure accurate capture and upload of paper source documents into eSource systems for audit readiness
  • 10Support IP accountability tasks under supervision and assist with regulatory compliance and protocol adherence

Requirements10

  • 1High school diploma or GED equivalent, Bachelor’s degree preferred
  • 2No prior clinical research experience required; training provided
  • 3Strong attention to detail, organization, and communication skills
  • 4Proficiency with Microsoft Office
  • 5Willingness to perform phlebotomy and clinical procedures as trained
  • 6Interest in learning clinical research operations and regulatory compliance
  • 7Ability to follow ICH-GCP guidelines and site SOPs
  • 8Comfort working onsite in Dallas, TX
  • 9Team-oriented mindset and proactive learner
  • 10Basic understanding of clinical research principles is a plus

Salary Insight

$40 - $48k per year

Location

Typeonsite
LocationDallas, Texas

Required Skills

Microsoft OfficePhlebotomyEDC systems
Share:

Similar open positions

Explore active roles that match your skills and interests.

System One

System One

19d agoDallas, Texascontract

Clinical Research Coordinator - System One

Join a busy onsite clinical research site in Dallas, TX as a Clinical Research Coordinator supporting vaccine and other clinical trials. You will coordinate study visits assist with informed consent maintain source documentation and ensure compliance with GCP SOPs. Partner with the PI research staff and participants to drive quality and patient experience.

26K–30K
Medical terminologyPatient careOrganizational skills+6 more

DYNAMED CLINICAL RESEARCH LP

8h agoPhoenix, Arizonafull-time

Research Assistant III, Lab at Dynamed Clinical Research

Owns data collection and regulatory support for clinical trials at a hospital-based site. Scale includes coordination of samples, study documentation, and site visits across multiple protocols. Works with the clinical research team and monitors to ensure compliance and data integrity. This role differs by combining hands-on patient interactions with regulatory documentation and data capture in EDC systems.

Competitive salary
phlebotomyedcivrs+2 more

Actalent

4h agoLos Angeles, Californiafull-time

Clinical Research Assistant, Oncology Trials & Phlebotomy

Onsite clinical research role supporting oncology trials at multiple LA area sites. Own patient visits, data collection, and regulatory tasks to enable study progress on ~45 active trials. This developmental position offers a clear path toward a Clinical Research Coordinator role within a collaborative team.

42K–52K
Clinical research coordinationPhlebotomyECG administration+7 more

Actalent

2d agoChicago, Illinoiscontract

Research Coordinator Actalent Chicago

Research Coordinator at Actalent in Chicago leads participant recruitment and data management for clinical trials. This role drives efficient study execution while ensuring regulatory compliance and high-quality data handling.

25K–30K
Clinical research coordinationParticipant recruitmentData entry+7 more

DocTrials

15d agoPhoenix, Arizonafull-time

Clinical Research Coordinator - DocTrials

Coordinate patient visits and lead interventional protocols at multiple Phoenix Valley offices. Manage patient acquisition and enrollment through community outreach while ensuring strict adherence to FDA and ICH-GCP guidelines. Consolidate study data and communicate updates via Basecamp.

Competitive salary
EDCGCPICF+10 more

Neurology Center of North Orange Co

8h agoLos Angeles, Californiafull-time

Clinical Research Coordinator, Neurology - LA Area & Onsite Phlebotomy Focus

Own clinical trial coordination for neurology studies at a Fullerton onsite site with direct interaction with investigators and subjects. You will manage visits, data integrity, and compliance for trials at scale, collaborating with a multidisciplinary team. The role emphasizes patient communication, privacy, and accurate documentation in ALCOA aligned systems. This position offers growth for individuals with 6+ months of clinical research exposure and a patient-centered approach.

50K–71K
IRB protocol complianceEDC system managementPhlebotomy+4 more