Clinical Research Coordinator Senior

This position serves as a Subject Matter Expert (SME) in managing clinical research studies at Intermountain Healthcare. The Senior Clinical Research Coordinator provides expertise, consultation, and management support for planning, implementing, and disseminating clinical research studies and initiatives, while training junior staff and supporting management in overseeing research operations.

Responsibilities

• Supports complex research studies across the Intermountain system with limited supervision, typically working on the most complex or largest programs. Acts as subject matter expert within study area and department domain.
• Provides oversight and/or supervision to existing clinical research coordinators. Assesses competency in lab sample handling and reinforcing training.
• Demonstrates in-depth knowledge of protocols, educates others, participates in oversight visits, and ensures compliance with patient privacy and research regulatory requirements. Disseminates information about the project. Utilizes GCP guidelines for patient screening, study procedures, data entry, and monitoring, supporting study team and investigator compliance.
• Screens participants for eligibility and commitment. Supports existing study coordinators with screening best practices and training.
• Facilitates strategies for study recruitment, participant retention, study execution, and program performance.
• Assists research manager in recruiting, managing workloads, caregiver check-ins, and team coaching. Helps to support team career development, enhancement, and engagement. Coordinates clinical patient information and assists physicians or residents.
• Teaches clinical research techniques, mentors new coordinators, ensures compliance with policies and regulations, and facilitates training, education, and development activities for the team.
• May perform ongoing Quality Assurance and evaluations at study completion. Monitors participant progression and conducts end-of-study evaluations. Organizes periodic data reviews for enrollment and compliance, compares data against project goals, and compiles enrollment data.
• Collaborates on issue resolution, maintains SOPs, participates in leadership meetings, manages study supplies, trains new hires, assesses coordinator needs, runs daily huddles, relays recognition, and assists in study prioritization when managers are unavailable. May contribute to writing reports, research papers, and other documentation of study results.

Requirements

• Extensive professional experience in a clinical research role requiring use of laboratory protocol, systems and documentation techniques, detailed knowledge of human subject research regulations, strong demonstrated attention to detail and ability to adhere to policies and procedures.
• Demonstrated experience working in a collaborative team environment.
• Experience using word processing, spreadsheet, database, internet and e-mail, and scheduling applications.
• Effective organizational skills; effective follow-through, and commitment to excellence.
• Effective professional communication skills; ability to communicate with others in a clear, understandable, and professional manner as well as strong interpersonal skills.
• Ability to work with personnel at all levels to gather information, communicate compliance requirements and handle complex issues within an often-sensitive political environment.

Preferred Qualifications

• Bachelor's Degree in a clinical or life science field, business, or healthcare operations. A degree must be obtained through an accredited institution.
• Experience in a healthcare or hospital setting.
• Multi-disciplinary knowledge of both health care and research.
• Expertise and/or experience in the clinical specialty or area of focus related to this research role (e.g., cardiology, pulmonary, oncology, women and newborn, etc.).

Skills

• Research protocols
• Documentation
• Clinical information systems
• Writing
• Verbal and written communication
• Patient Information
• Planning ability
• Leadership
• Critical Thinking
• Detail Oriented

Physical Requirements

• Ongoing need to see and read information, labels, monitors, etc., and to identify equipment and supplies.
• Frequent interactions requiring verbal communication, hearing, and understanding spoken information, alarms, needs, and issues quickly and accurately.
• Manual dexterity of hands and fingers to manipulate complex and delicate equipment with precision and accuracy, including frequent computer use and typing.
• Expected to bend, lift, and carry patient files, documents, equipment, and supplies.
• Remain sitting or standing for long periods of time while interacting with others or performing work on a computer, telephone, or other equipment.
• For roles requiring driving: Expected to drive a vehicle which requires sitting, seeing, and reading signs, traffic signals, and other vehicles.

Pay

The hourly range for this position is $31.01 - $48.84. Actual hourly rate dependent upon experience.

Schedule

Monday - Friday, 8am to 5pm. Scheduled weekly hours: 40.

Benefits

We provide a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.