Adams Clinical
Clinical Research Coordinator II
Dallas, Texas, United States · Mid
Sponsorship not specified$23k-$28kDetected 1 day ago
Clinical TrialsClinical ResearchPharmacy PracticeResearchLeadershipCommunicationCollaboration
About the 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, supporting both inpatient and outpatient studies.
- We are seeking experienced applicants for the Clinical Research Coordinator II role at our Dallas location.
- This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.
Responsibilities
- Independently manage a portfolio of complex and/or high-volume trials with guidance from a CRC III or the Site Manager, leading all operational and visit-related activities.
- Fully own study execution, including screening operations, enrollment progress, screening vs. target metrics, and SCF rates.
- maintain quality and performance oversight.
- Lead data entry and query resolution efforts, ensuring high data quality and inspection readiness.
- Maintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs.
- Identify operational risks and propose corrective actions to maintain study timelines and quality.
- Train and supervise CRC I's or RA's supporting the portfolio; maintain quality and performance oversight.
Requirements
- Bachelor's degree required.
- At least 1 year of prior clinical research experience.
- Experience with industry-sponsored clinical trials required.
- Lead study start-up activities for assigned studies, including SIV preparation, regulatory readiness, supply planning, and supporting site completion of required staff training.
- At least 1 year of prior clinical research experience. Experience with industry-sponsored clinical trials required.
- Demonstrated ability to manage complex studies independently.
- Strong communication skills and comfort interacting directly with sponsors.
- Pay: $23.00 - $28.37 per hour
- Benefits:
- 401(k) matching
- Medical, Dental, & Vision insurance
- Employee assistance program
- Flexible spending account
- Health insurance
Compensation
- $23.00 - $28.37 per hour
Benefits
- Parental leave
Company info
- 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.
Equal opportunity
- equal opportunity and affirmative action employer.
Visa & Work Authorization
- entation, 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
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