Senior Clinical Research Lead — Trials & Data Quality

ALLIANCE CLINICAL LLC; Lewisville (TX); On-site; USD 65,000 - 95,000; Full time

Job summary

Alliance Clinical Network in Lewisville, TX, is seeking a Senior Clinical Research Coordinator to oversee planning and management of study projects, ensuring compliance with protocols and regulatory requirements. The Senior CRC coordinates study activities, manages data collection, supports investigators with reporting and documentation, and leads a team to maintain high quality research operations.

It also requires interaction with sponsors, CROs, and IRBs to ensure timely start-up and

Qualifications

• Associate's degree and/or accreditation in healthcare or related field.
• Ability to lead and direct employees.
• Experience with FDA, GCP and confidentiality.

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 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.

Skills

Leadership

Communication

Time management

Prioritization

Team coaching

GCP knowledge

Attention to detail

Multi-tasking

Emotional intelligence

Education

Associate's degree or healthcare certification

Job description

Alliance Clinical Network in Lewisville, TX, is seeking a Senior Clinical Research Coordinator to oversee planning and management of study projects, ensuring compliance with protocols and regulatory requirements. The Senior CRC coordinates study activities, manages data collection, supports investigators with reporting and documentation, and leads a team to maintain high quality research operations.

It also requires interaction with sponsors, CROs, and IRBs to ensure timely start-up and