Regional Clinical Research Manager at ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC

Phoenix, Arizona, United States -

Full Time

Start Date

Immediate

Expiry Date

20 May, 26

Salary

112000.0

Posted On

19 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Staff Management, Training, Mentorship, Workload Balancing, Clinical Trial Management System, Data Capture Systems, Metric Review, Site Operations Management, Budget Management, Vendor Onboarding, Protocol Compliance, ICH-GCP Standards, Quality Assurance, Site Visits, Issue Resolution

Industry

Hospitals and Health Care

Description

Description Title: Regional Clinical Research Manager Location: 4550 East Bell Road, Suite 170, Phoenix, AZ 85032 Description: Telework permitted, Arizona Arthritis & Rheumatology Associates, P.C. (Phoenix, AZ) seeks a Regional Clinical Research Manager to serve as a first line manager to research coordinators and assistants; conduct training and mentorship of new clinical research staff; assign tasks and studies to ensure workloads are balanced among coordinators and assistants; utilize Clinical Trial Management System weekly to ensure productivity goals are met; monitor electronic source data capture system reports to ensure data and query goals are met; meet with employees monthly to review metrics and conduct weekly huddles with the team; manage operations at the clinical sites and facilitate all medical staff’s participation in research; implement Clinical Trial Agreements & Budgets and ensure model fiscal operations; assist with qualifying and onboarding vendors and staff for clinical services as required per study; approve and order supplies and equipment as needed from sponsors and vendors; ensure clinical research staff have the skills and resources necessary for success; ensure clinical sites have the medical equipment and resources necessary for success; ensure clinical sites are engaging in recruitment activities and meeting patient enrollment goals; facilitate operational changes using professional and positive motivation; ensure compliance with research protocols, handbook policies, standard operating procedures, ICH-GCP Standards, FDA regulations, and medical laws, and implement solutions for compliance; perform quality assurance and complete corrective action and prevention assessment plans; conduct Pre-Study Visits and Site Initiation Visits for new clinical trials; serve as an escalation point for all clinical trials and the first point of contact for site staff members; provide ongoing support, needs assessment, and issue resolution to clinical sites and staff on an ongoing basis, and escalate to Director of Clinical Research when needed; communicate with physicians, vendors, sponsors, and CROs to address and resolve issues; collaborate with fellow Regional Research Managers to ensure a consistent and coordinated department and management style across all sites nationally; meet with administrative staff regularly to ensure all research operations are running smoothly; and perform duties for coordinators and managers when there is a lapse in coverage. Bachelor’s degree in Biomedical Science, Physiology, Nursing, Medicine, Clinical Research, or a related field; two years’ relevant experience; strong experience with clinical research and relevant clinical indications; knowledge of specific state and federal regulations governing clinical research and privacy; strong verbal and written communication skills; strong knowledge of medical procedures and clinical terminology; strong knowledge of ICH-GCP guidelines; and up to 20% domestic travel required. Salary ranging $109,678.00/yr. to $112,000.00/yr.

Responsibilities

This role involves serving as a first-line manager for research staff, overseeing daily operations, assigning tasks, and ensuring productivity and data goals are met using relevant systems. The manager must also facilitate medical staff participation in research, manage budgets, ensure compliance with all regulations, and provide ongoing support and issue resolution to clinical sites.