Senior Clinical Research Coordinator

Alliance Clinical Network; Lewisville (TX); On-site; USD 60,000 - 90,000; Full time

Job summary

Alliance Clinical Network seeks a Senior Clinical Research Coordinator to oversee planning and management of study projects, ensure protocol/regulatory compliance, and support investigators with reporting and documentation.

The Senior CRC coordinates study activities, manages data collection, and maintains the integrity and efficiency of research operations, working with CROs, CRA teams, and IRBs.

Qualifications

• Associate’s degree or completion of an 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.

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.

Skills

Team leadership

Communication skills

Time management

Attention to detail

Multi-tasking

Adaptability

Clinical research knowledge

Education

Associate degree

Healthcare certification program

Job description

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.

• 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.

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.