Clinical Research Coordinator

Job Description

Job Description

Bilingual Clinical Research Coordinator

Overview

Seeking a Clinical Research Coordinator to manage day-to-day clinical trial activities at a multi-level site. This role requires full-scope coordination, including patient interaction, regulatory work, and data management. Must be comfortable using stairs between floors.

Key Responsibilities

• Oversee clinical trial operations in compliance with GCP and FDA guidelines
• Obtain informed consent and perform study visits per protocol
• Perform phlebotomy procedures
• Collect, enter, and manage study data
• Support patient recruitment and engagement
• Maintain regulatory documentation and study records
• Manage investigational product (receipt, storage, dispensing, accountability)
• Coordinate lab samples (processing, shipping, reporting)
• Monitor participant compliance and study adherence
• Ensure study supplies and equipment are maintained

Qualifications

• Minimum 2 years of Clinical Research Coordinator experience
• Bilingual (English/Spanish) required
• Phlebotomy experience required
• Knowledge of GCP and FDA regulations
• Strong attention to detail and organizational skills
• Proficient with data entry and clinical systems

Job Type & Location

This is a Contract to Hire position based out of Hollywood, FL.

The pay range for this position is $28.00 - $33.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Hollywood,FL.

This position is anticipated to close on May 29, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.