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Research Coordinator Jobs in Puerto Rico (NOW HIRING)

Genco

PR · On-site

$45K - $55K/yr

Hybrid Position The Legal and Compliance Coordinator provides comprehensive legal support and ... Research requirements for compliantly doing business in new jurisdictions. * Research required ...

Bio-Nuclear of Puerto Rico

PR · On-site

$13.50 - $17/hr

The Coordinator assigned to Application Specialists shall:a. Keep the Application Specialists ... Research flight, hotel, and transportation information to refer to the CEO's Administrative ...

MAPEI Corporation

Marketing Coordinator

Dorado, PR · On-site

$37K - $51K/yr

... with researching industry trends, content ideas, and best practices to support marketing ... Support the development and coordination of written content for social media, website updates ...

Moriah Engineering

PR · On-site

Position Overview The Project Coordinator will support the execution of capital and operational projects within a regulated manufacturing/pharmaceutical environment. This role is primarily field ...

Moriah Engineering

PR

Position Overview The Project Coordinator will support the execution of capital and operational projects within a regulated manufacturing/pharmaceutical environment. This role is primarily field ...

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Research Coordinator information

What is a research coordinator?

A research coordinator supervises the daily activities of a study and monitors the activities of the subjects and researchers. As a research coordinator, your duties revolve around making sure that the study is conducted ethically and does not violate the research guidelines of the governing board or other agency. In short, you are responsible for making sure the study has as few flaws in its methodology as possible. You are also in charge of most administrative tasks. In this role, you can work on medical, technological, psychological, or other types of research projects, but you may work on clinical research most often.

Are clinical research coordinators in high demand?

Clinical research coordinators are in high demand due to the growth of clinical trials and medical research. They are essential for managing study protocols, ensuring compliance, and coordinating between research teams and participants, which makes their skills highly sought after in healthcare and research institutions.

What are some common challenges research coordinators face when managing multiple studies simultaneously?

Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with regulatory requirements, and managing communication among diverse stakeholders. Staying organized with detailed documentation and proactive scheduling is essential to prevent protocol deviations. Effective collaboration with principal investigators, sponsors, and clinical staff also helps to navigate unexpected changes and maintain study integrity.

What is the difference between Research Coordinator vs Research Assistant?

AspectResearch CoordinatorResearch Assistant
Required CredentialsBachelor's degree often required; some roles prefer or require a master'sTypically an undergraduate student or recent graduate; some roles may require a bachelor's degree
Work EnvironmentLeads study activities, manages protocols, interacts with stakeholdersSupports data collection, literature review, and administrative tasks
Employer & Industry UsageUsed in clinical, academic, and industry research settingsCommonly found in academic labs and research projects

The Research Coordinator generally has more responsibilities, including managing study protocols and liaising with stakeholders, while the Research Assistant provides support with data collection and administrative tasks. Both roles are essential in research projects but differ in scope and level of responsibility.

What skills should I have to be a successful clinical research coordinator?

To thrive as a Research Coordinator, you need strong organizational abilities, attention to detail, and a relevant bachelor's degree or higher in a scientific or health-related field. Familiarity with research compliance systems, data management tools, and Institutional Review Board (IRB) protocols is commonly required. Excellent communication, problem-solving, and multitasking skills help you manage studies and collaborate effectively with diverse teams. These skills ensure the smooth execution of research projects, regulatory compliance, and the reliability of study outcomes.

What qualifications do you need to be a research coordinator?

Research coordinators typically need a bachelor's degree in a health-related field such as biology, nursing, or public health. Relevant skills include strong organizational abilities, attention to detail, and familiarity with clinical trial protocols and data management tools. Some positions may require certification, such as the Certified Clinical Research Professional (CCRP).

What does a research coordinator do?

A research coordinator manages and oversees clinical or scientific research studies, ensuring they follow protocols, regulatory requirements, and ethical standards. They coordinate activities such as participant recruitment, data collection, and documentation, often using tools like electronic health records or research databases. Strong organizational skills and knowledge of research regulations are essential for this role.
More about Research Coordinator jobs
What are the most commonly searched types of Research jobs in Puerto Rico? The most popular types of Research jobs in Puerto Rico are:
What job categories do people searching Research Coordinator jobs in Puerto Rico look for? The top searched job categories for Research Coordinator jobs in Puerto Rico are:
Research Coordinator jobs near you
Infographic showing various Research Coordinator job openings in Puerto Rico as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Spanish Bilingual Clinical Research Coordinator - Dorado, Puerto Rico

IQVIA

San Juan, PR • On-site

$41K - $118K/yr

Part-time

Medical, Life

This job post has expired today. Applications are no longer accepted.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

59th of 221 rated it services

Job description

Spanish Bilingual Clinical Research Coordinator- Dorado, Puerto Rico
Work Setup: On-site
Schedule: Part-time, 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device companies to advance healthcare and improve patient outcomes. By combining deep scientific expertise with innovative technologies, IQVIA delivers the highquality evidence needed to drive clinical development forward.

About the Role

IQVIA is seeking a Spanish Bilingual Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This handson role is ideal for a detailoriented professional with prior coordinating experience who is comfortable working directly with patients, managing study data, and ensuring strict adherence to study protocols and Good Clinical Practice (GCP).

The CRC plays a critical role in the daytoday execution of clinical trials, patient safety, and data integrity.

Key Responsibilities

  • Conduct and support participant visits, including clinical procedures such as ECGs, vital signs, and biological sample collection

  • Coordinate study activities in compliance with protocols, GCP, and regulatory requirements

  • Prepare study materials, organize equipment, and support logistical planning for study visits

  • Assist with patient recruitment, screening, consent, and visit coordination

  • Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation

  • Maintain investigational product (IP) accountability, including reconciliation and documentation

  • Conduct chart reviews to support eligibility determination and data verification

  • Collaborate closely with investigators, sponsors, and monitors to resolve study issues and maintain data quality

  • Serve as a patient advocate, ensuring participant safety, comfort, and confidentiality

  • Uphold Health & Safety and quality standards across all study activities

Qualifications & Experience

  • Bachelor's degree preferred, or an equivalent combination of education and relevant experience

  • Minimum of 1+ year of handson clinical research coordinating experience

  • Demonstrated experience with:

    • Patient-facing study visits

    • EDC data entry and query resolution

    • Patient recruitment and screening

    • Investigational Product (IP) accountability

    • Source document and chart review

  • Working knowledge of clinical trials, GCP, and medical terminology

  • Strong attention to detail with the ability to manage multiple priorities

  • Ability to build effective working relationships with study teams and participants

  • Fluency in Spanish required (spoken and written); English proficiency preferred

  • Comfortable working on-site and independently within a structured research environment

Additional Information

  • This is an on-site, part-time position (24 hours/week)

  • Not eligible for visa sponsorshi

#LI-CES and #LI-DNP #LI-HCP #remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $41,000.00 - $118,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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