Senior Clinical Research Coordinator

ALLIANCE CLINICAL LLCLewisville, TX

About The Position

The Senior Clinical Research Coordinator (Senior CRC) oversees the planning and management of study projects, ensuring compliance with protocols and regulatory requirements. This role coordinates the study activities, manages data collection, and supports investigators with reporting and documentation. The Senior CRC plays a critical role in maintaining the integrity and efficiency of research operations.

Requirements

  • Associate’s degree and/or completion of accredited healthcare certification program.
  • Ability to effectively lead, coach and direct employees.
  • Strong leadership skills that empower an engaged and effective team.
  • Exceptional communication skills, including verbal and written communication.
  • Ability to prioritize critical tasks and effectively manage time.
  • Minimum of 2 years of experience in clinical research.
  • Comprehensive knowledge of FDA, GCP & confidentiality.
  • Exceptional attention to detail and strong organizational skills.
  • Proven ability to multi-task in a rapidly changing environment.
  • High emotional intelligence, with the ability to identify and effectively control stressful situations.

Nice To Haves

  • Minimum of 2 years of experience working as a Clinical Research Coordinator preferred.

Responsibilities

  • Provide work directions to clinical staff and back-office team.
  • Provide operational leadership to resolve complex study and site-level issues impacting enrollment, compliance, and timelines.
  • Review, comprehend, and communicate study protocols.
  • Oversee SIV, PSV and IMV.
  • Assist CRC team as needed to facilitate research and business needs.
  • Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOPs.
  • Oversee data quality and ensure accuracy and timelines of study data across assigned protocols.
  • Work closely with CRO/CRA and IRB.
  • Manage required study start up documentation, training, and timelines on assigned study protocols.
  • Effectively communicate with sponsors, ensuring customer satisfaction.
  • Direct study resource planning and ensure appropriate allocation of supplies and equipment.
  • Perform other duties as assigned.
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