Clinical Research Coordinator: Startups & Compliance

Nnphi

San Juan (PR)

On-site

USD 52,000 - 76,000

Full time

12 days ago

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

PRCCI in San Juan, Puerto Rico, is seeking a Clinical Research Coordinator to support the PI and project team across startup, recruitment, coordination, data management, and regulatory tasks for NIH- and FDA-guided studies.

You will ensure compliance with ICH-GCP, maintain study documents, manage budgets and reporting, and liaise with investigators, sponsors, and clinical staff. A BA/BS in a health field and relevant experience are required; bilingual English/Spanish preferred.

Qualifications

  • Excellent written and verbal communication in English and Spanish.
  • Experience in clinical trials research or related field.
  • Ability to work in a fast-paced, collaborative environment.
  • Familiar with NIH, FDA, ICH-GCP guidelines and regulatory practices.

Responsibilities

  • Coordinate startup activities including regulatory submissions and site initiation.
  • Identify and screen participants; obtain informed consent.
  • Schedule visits, collect data, and manage samples as required.
  • Maintain regulatory documents and assist with audits.
  • Track budget, expenses, and study metrics; generate reports.
  • Communicate with investigators, sponsors, and staff to ensure smooth operations.
  • Train site staff on protocol, procedures, and compliance as needed.

Skills

Bilingual English/Spanish
Time management
Team collaboration
Customer service
Tech proficiency: MS 365, Google,Share

Education

BA/BS in health-related field
3+ years clinical trials exp.

Tools

CTMS

Job description

PRCCI in San Juan, Puerto Rico, is seeking a Clinical Research Coordinator to support the PI and project team across startup, recruitment, coordination, data management, and regulatory tasks for NIH- and FDA-guided studies.

You will ensure compliance with ICH-GCP, maintain study documents, manage budgets and reporting, and liaise with investigators, sponsors, and clinical staff. A BA/BS in a health field and relevant experience are required; bilingual English/Spanish preferred.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Research Coordinator: NIH Trials & Study Ops
Clinical Research Coordinator: NIH Trials & Study Ops

PRCCI • San Juan (PR)

On-site
USD 45,000 - 65,000
Bilingual Clinical Research Coordinator
Bilingual Clinical Research Coordinator

Puerto-Rico-Science-Technology- • San Juan (PR)

On-site
USD 42,000 - 60,000
Clinical Trials Coordinator: Research Operations
Clinical Trials Coordinator: Research Operations

Automatic Data Processing, Inc. • San Juan (PR)

On-site
USD 50,000 - 65,000
Clinical Trials Site Lead — Regulatory & Operations
Clinical Trials Site Lead — Regulatory & Operations

PRCCI • San Juan (PR)

On-site
USD 110,000 - 140,000
Clinical Research Coordinator
Clinical Research Coordinator

Nnphi • San Juan (PR)

On-site
USD 52,000 - 76,000
Clinical Research Coordinator
Clinical Research Coordinator

Puerto-Rico-Science-Technology- • San Juan (PR)

On-site
USD 42,000 - 60,000
Clinical Research Coordinator
Clinical Research Coordinator

PRCCI • San Juan (PR)

On-site
USD 45,000 - 65,000
Clinical Trials Operations Lead & Regulatory Manager
Clinical Trials Operations Lead & Regulatory Manager

Nnphi • San Juan (PR)

On-site
USD 85,000 - 105,000
Clinical Trials Site Lead & Regulatory Manager
Clinical Trials Site Lead & Regulatory Manager

Puerto-Rico-Science-Technology- • San Juan (PR)

On-site
USD 90,000 - 130,000
Clinical Research Coordinator
Clinical Research Coordinator

Automatic Data Processing, Inc. • San Juan (PR)

On-site
USD 50,000 - 65,000