Top 6 Clinical research operations manager Jobs in Florida

Clinical Research Operations Manager
Nextgen Research Group LLC —Miami, FL
- Full-time
- Background check
- Spanish
- Pass drug screening
Clinical Research Operations Manager
AdventHealth Orlando Support —Celebration, FL
- $79,402.93 - $147,697.47 a year
- Full-time
- Background check
- CPR Certification
- Nursing
- Paid parental leave
- Disability insurance
10d
Clinical Research Operations Manager
Melgar-Caro Medcenter and Community research —Miami, FL
- $62,000 - $80,000 a year
- Full-time
- Bilingual
- Management
- Patient monitoring
Quick Apply
12d
Research Operations Manager - Cancer Institute (Full Time, Days)
Nicklaus Children's Hospital —Miami, FL
- Full-time
- Writing skills
- Master's degree
- Analysis skills
Medical Center Operations Manager
MCI —Miami, FL
- Full-time
- Spanish
- Microsoft Excel
- Microsoft Outlook
Quick Apply
8d
SUPERVISOR CLINICAL RESEARCH OPERATIONS PRE AWARD
Moffitt Cancer Center —Tampa, FL
- $82,934.80 - $126,427.60 a year
- Full-time
- Nursing
- Finance
- Analysis skills

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Clinical Research Operations Manager
Nextgen Research Group LLC —Miami, FL
Minimum of 2 years of clinical research experience, including experience coordinating clinical trials. The ideal candidate is an experienced clinical researcher…
Clinical Research Operations Manager
AdventHealth Orlando Support —Celebration, FL
Collaborates with managers in Research Services, Study Intake, Portfolio Management, and clinical study coordinators to develop study budgets for all research…
$79,402.93 - $147,697.47 a year
10d

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Clinical Research Operations Manager

Nextgen Research Group LLC
Miami, FL

Apply Now

Job Details

Full-time

Qualifications

Research project management
Document compliance management
Spanish
Medical software
HIPAA
Filing
English
Schedule management
ICH guidelines
Communication with regulatory authorities for clinical trials
Productivity software
Clinical quality assurance standards
FDA regulations
Research compliance quality assurance records management

Full Job Description

Description:

NextGen Research Group is seeking a bilingual (English/Spanish), highly organized, proactive, and experienced Clinical Research Operations Manager to oversee the daily operations of our growing clinical research site. This leadership role is responsible for ensuring the efficient management of office operations, supporting business development and study startup activities, maintaining regulatory compliance, and providing clinical research coordination support when needed. The ideal candidate is an experienced clinical researcher who enjoys building relationships with sponsors and CROs and can balance operational oversight with hands-on study coordination.

Responsibilities include, but are not limited to:

Research Operations

Oversee the day-to-day administrative and operational functions of the clinical research site.
Develop and maintain efficient workflows to support research operations.
Ensure compliance with FDA, GCP, HIPAA, IRB, and sponsor requirements.
Assist with the implementation and maintenance of Standard Operating Procedures (SOPs).
Monitor site performance and identify opportunities for operational improvements.
Coordinate office resources, vendors, supplies, and equipment to support research activities.

Study Startup & Business Development

Complete feasibility questionnaires and sponsor surveys.
Assist with study feasibility assessments and site selection activities.
Prepare and submit study applications to sponsors and CROs.
Support study startup activities, including regulatory document collection and essential document preparation.
Assist with site qualification, initiation, and monitoring visits.
Maintain positive relationships with sponsors, CROs, investigators, and research partners.
Attend local and national clinical research conferences, investigator meetings, and industry events to represent NextGen Research Group and cultivate relationships with sponsors, CROs, and research partners.

Clinical Research Coordination

Coordinate assigned clinical research studies as needed.
Screen, recruit, consent, enroll, and retain study participants.
Schedule participant visits and ensure protocol-required procedures are completed.
Maintain accurate source documentation, electronic case report forms (eCRFs), and regulatory files.
Ensure protocol compliance and timely resolution of data queries.
Conduct participant follow-up and maintain excellent participant engagement.
Serve as a liaison between investigators, sponsors, CROs, and study participants.

Leadership & Administrative Support

Assist with training and mentoring research staff.
Support investigators and leadership with operational planning and project management.
Track study milestones, enrollment goals, and startup timelines.
Participate in quality assurance activities and prepare for sponsor audits and regulatory inspections.
Maintain confidentiality of participant and study information.

Perform other duties as assigned.

Requirements:

Qualifications

Bilingual (English/Spanish) required.
Bachelor's degree preferred; equivalent clinical research experience will be considered.
Minimum of 2 years of clinical research experience, including experience coordinating clinical trials.
Experience with study startup activities, regulatory submissions, and sponsor/CRO communications preferred.
Thorough understanding of ICH-GCP, FDA regulations, HIPAA, and IRB requirements.
Experience maintaining regulatory documentation and study essential documents.
Strong organizational, project management, and problem-solving skills.
Excellent written and verbal communication skills.
Strong interpersonal skills with the ability to build relationships with sponsors, CROs, investigators, and participants.
Ability to manage multiple projects and priorities simultaneously while meeting deadlines.
Proficiency with Microsoft Office Suite and clinical research software (CTMS, eSource, eRegulatory, EDC systems preferred).
Ability to travel occasionally for industry conferences and sponsor meetings (~10%).
Must be able to pass a drug test and background screening. You may visit the Florida

Care Provider Background Screening Clearinghouse for more information.

We are a Drug-Free Workplace and are committed to providing equal employment opportunities to all applicants and employees without regard to age, disability, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, national origin, veteran or military status, genetic information, or any other protected status under applicable federal, state, or local law.

Apply Now

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clinical research operations manager jobs in florida

Clinical Research Operations Manager

Clinical Research Operations Manager

Clinical Research Operations Manager

Research Operations Manager - Cancer Institute (Full Time, Days)

Medical Center Operations Manager

SUPERVISOR CLINICAL RESEARCH OPERATIONS PRE AWARD

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