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Senior Clinical Research Coordinator

ALLIANCE CLINICAL LLC
Posted a month ago, valid for 8 days
Location

Lewisville, TX, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The Senior Clinical Research Coordinator (Senior CRC) is responsible for overseeing the planning and management of study projects while ensuring compliance with protocols and regulatory requirements.
  • Candidates must have a minimum of 2 years of experience in clinical research, with 2 years preferred as a Clinical Research Coordinator.
  • This role involves coordinating study activities, managing data collection, and providing operational leadership to resolve complex issues impacting enrollment and compliance.
  • The position requires an associate's degree or completion of an accredited healthcare certification program, along with strong leadership and communication skills.
  • Salary details are not specified, but the company emphasizes a commitment to integrity and excellence in advancing medical research.


Summary:

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.

Essential Duties and 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.

Qualifications:

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


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.





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