Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Barrington James

Director of Clinical Operations

Career Insights for Clinical Director

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Florida data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Clinical Director directs and manages a medical practice, clinic, hospital, or other clinical setting. Organizes and manages of staff physicians, policy implementation, and ensures that standards for medical care are communicated and maintained.

$119,292 / year median in Florida

+17% projected growth

Explore Career

Job Description

Director of Clinical Operations at Barrington James Director of Clinical Operations at Barrington James in Coral Gables, Florida Posted in 5 days ago.
Type:
full-time
Job Description:
Our client is seeking a Director/Manager of Clinical Operations, Phase I, to oversee clinical trials, ensure protocol adherence, and manage staff and operational aspects of studies. Requires strict compliance with
GCP, ICH
guidelines and company SOPs, with core duties spanning staff management, protocol review, quality assurance and study supervision. Responsibilities Lead and mentor the clinical operations team, fostering a collaborative and efficient environment Ensure protocol compliance and maintain high quality standards across studies Partner with Principal Investigators and the Site Director to assign studies and develop enrollment strategies Oversee HR functions including staff evaluations, recruitment and training Monitor protocol adherence and report deviations to sponsors and regulatory bodies Coordinate with the Site Director and Principal Investigators to assign clinical research coordinators Review study components with PIs and Site Directors ahead of study initiation Conduct study closeout procedures Ensure compliance with FDA, ICH and GCP regulations Minimum qualifications Bachelor's degree in a scientific or healthcare related field Phase I or early phase experience 7-10 years of clinical operations experience, including 5+ years in a senior leadership role Strong understanding of FDA, ICH and GCP regulations and guidelines Strong communication, organisational and leadership skills Proficiency in Microsoft Word, Excel and clinical trial management software In-depth knowledge of clinical trial operations, including study start-up, site selection, patient recruitment, monitoring, data management and study close-out Experience managing and mentoring a team of clinical operations professionals Bilingual in English and Spanish