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Clinical Trials Manager Jobs in Puerto Rico (NOW HIRING)

IQVIA

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

... high-quality clinical trials. In this role, you'll partner with investigative sites and cross ... Track and manage study progress, including regulatory approvals, enrollment milestones, and data ...

Organon

Medical Science Liaison - Florida

Florida, PR · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Managed Markets Customers; helps to identify pre-clinical, clinical and post-marketing study ... trials and collaboration with Clinical Development colleagues on investigator selection ...

Organon

Medical Science Liaison - Florida

Florida, PR

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Managed Markets Customers; helps to identify pre-clinical, clinical and post-marketing study ... trials and collaboration with Clinical Development colleagues on investigator selection ...

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Clinical Trials Manager information

What does a clinical trials manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are some common challenges faced by clinical trials managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.

What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Trials jobs in Puerto Rico?

The most popular types of Clinical Trials jobs in Puerto Rico are:

What are popular job titles related to Clinical Trials Manager jobs in Puerto Rico?

For Clinical Trials Manager jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Clinical Trials Manager jobs in Puerto Rico look for?

The top searched job categories for Clinical Trials Manager jobs in Puerto Rico are:

Clinical Trials Manager jobs near you
Infographic showing various Clinical Trials Manager job openings in Puerto Rico as of June 2026, with employment types broken down into 3% As Needed, 56% Full Time, and 41% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

CRA 2/Senior CRA 1

IQVIA

San Juan, PR • On-site

$76K - $175K/yr

Full-time

Posted 27 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

Join a Team That's Advancing Clinical Research

We're looking for a passionate and driven Clinical Research Associate (CRA) based in Puerto Rico to join our team and play a key role in delivering high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and a strong focus on patient outcomes.

What You'll Do
  • Lead and execute site monitoring visits, including selection, initiation, routine monitoring, and close-out visits, in accordance with GCP/ICH guidelines.
  • Build strong relationships with investigative sites to drive site performance, patient recruitment, and study engagement.
  • Ensure protocol compliance, data integrity, and high-quality study execution.
  • Proactively identify risks, resolve issues, and escalate concerns when appropriate.
  • Track and manage study progress, including regulatory approvals, enrollment milestones, and data quality metrics.
  • Maintain accurate study documentation and contribute to audit and inspection readiness.
  • Collaborate with cross-functional teams to support successful study delivery and timeline achievement.
What You Bring
  • Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field (or equivalent experience).
  • Minimum of 1.5 years of on-site monitoring experience as a Clinical Research Associate.
  • Fluency in both English and Spanish (written and verbal) required.
  • Experience monitoring studies in CNS, Cardiovascular, Obesity, and/or MASH/NASH therapeutic areas preferred.
  • Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
  • Excellent communication, relationship-building, problem-solving, and organizational skills.
  • Ability to effectively manage multiple priorities in a fast-paced environment.
  • Ability and willingness to travel as required within Puerto Rico and potentially other locations as needed.
Why Join Us
  • Make a direct impact on advancing clinical research and improving patient outcomes.
  • Work alongside experienced, collaborative, and mission-driven teams.
  • Access opportunities for professional growth and career development.
  • Thrive in a dynamic environment where your expertise and contributions truly matter.
Ready to Make an Impact?

If you're ready to take the next step in your CRA career and contribute to meaningful clinical research, we'd love to hear from you. Apply today and help bring innovative therapies to patients who need them most.

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 $76,300.00 - $175,100.00. 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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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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