Site Management Lead

Talent Groups; United States; On-site; USD 16,740 - 42,408; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A clinical research organization is seeking a Regional Site Management Lead to oversee clinical trials. Ideal candidates will have over 6 years of clinical research experience, including site monitoring responsibilities, and must be open to travel up to 50%. Strong communication and organizational skills are essential for this mid-senior level role based in Fort Lauderdale, FL. Benefits include medical insurance and a 401(k).

Qualifications

• 6+ years of clinical research experience, including direct site monitoring.
• 3+ years in a lead CRA or monitoring oversight capacity required.
• Willingness to travel up to 50% based on study needs.

Responsibilities

• Oversee operational delivery of clinical trials across all phases.
• Ensure timely startup, patient recruitment, and study close-out.
• Maintain continuous monitoring oversight and inspection readiness.

Skills

Clinical research experience

Site monitoring (CRA) responsibilities

Stakeholder engagement skills

Written and verbal communication

Organizational skills

Education

Bachelor’s degree in healthcare or life sciences

Job description

Overview

We are seeking a Regional Site Management Lead to join our Clinical Operations team. This pivotal role serves as the regional representative responsible for overseeing the operational delivery of clinical trials across all phases. You will work closely with investigator sites, CROs, and internal stakeholders to ensure timely startup, patient recruitment, database lock, and study close-out, while ensuring continuous monitoring oversight and inspection readiness.

Qualifications

• Bachelor’s degree in a healthcare or life sciences field (advanced degree preferred).
• Minimum 6+ years of clinical research experience, including direct site monitoring (CRA) responsibilities.
• At least 3+ years in a lead CRA, CRA manager, or monitoring oversight capacity.
• Deep understanding of regional clinical research guidelines and trial execution strategies.
• Proven ability to work cross-functional in a matrixed, global environment.
• Strong written and verbal communication, organizational, and stakeholder engagement skills.
• Willingness and ability to travel up to 50% or more based on study needs.

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Research and Science

Industries

• Staffing and Recruiting, Pharmaceutical Manufacturing, and Biotechnology Research

Location

Fort Lauderdale, FL

Salary

$1,500 - $3,800

Benefits

• Medical insurance
• Vision insurance
• 401(k)