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Clinical Research Jobs in Puerto Rico (NOW HIRING)

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites.Participates in internal meetings and workstreams as SME for monitoring processes andSystems.

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites.Participates in internal meetings and workstreams as SME for monitoring processes and Systems.

IQVIA

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

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 ...

IQVIA, Inc.

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

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 ...

IQVIA

CRA 2/Senior CRA 1

San Juan, PR · On-site

$76K - $175K/yr

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 ...

Boston Scientific

Collaborate with cross-functional teams (sales, marketing, clinical research, technical support) to develop optimal customer solutions. Actively contributes to regional strategy execution ...

Organon

Medical Science Liaison - Florida

Florida, PR · On-site

Clear understanding of clinical research methodologies and ability to independently evaluate and translate scientific material in an effective credible manner. * Ability to travel locally, regionally ...

Organon

Medical Science Liaison - Florida

Florida, PR · On-site

Clear understanding of clinical research methodologies and ability to independently evaluate and translate scientific material in an effective credible manner. * Ability to travel locally, regionally ...

TPIS

Clinical Review Nurse

San Juan, PR · On-site

$57.86/hr

Clinical Review Nurse San Juan, PR, PR Salary: $21.00 Annually This role investigates Health Insurance Waste and Error stopped claims by gathering information, researching state and federal ...

New

Diverse-Lynx

Google Cloud Platform Engineer

Aguadilla, PR · On-site

$69 - $73/hr

Experience supporting Life Sciences, Clinical, R&D platforms. * Understanding of GxP, CSA/CSV validation, and regulated cloud environments. * Knowledge of data governance, privacy, and compliance ...

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All JobsClinical Research JobsClinical Research Jobs in Puerto Rico

Clinical Research information

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What is the difference between Clinical Research vs Clinical Data Coordinator?

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research jobs

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

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

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

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

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

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

Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Puerto Rico as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Physician, MD/DO - Clinical Research

Headlands Research

San Juan, PR • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 25 days ago

Key responsibilities

  • Lead and oversee clinical trials at the site, ensuring compliance with protocols, regulatory standards, and ethical guidelines.

  • Provide leadership, mentorship, and training to research staff to support high-quality study execution.

  • Obtain IRB approval for study initiation and protocol modifications, and communicate with stakeholders including sponsors, monitors, and regulators.

Job description

 Location: San Juan, PR  | Site Name: CMR Center  | Full-Time  | Clinical Research

We're seeking an experienced physician for our clinical research site located in San Juan, PR to serve as our Principal Investigator on clinical trials. The Principal Investigator is responsible for ensuring subject safety, protocol compliance, data integrity, and high-quality study execution in accordance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and company standards. 

This role is ideal for a physician who is interested in clinical research, passionate about improving patient access to innovative therapies, and helping expand research opportunities in the community. In addition to clinical and study oversight responsibilities, the Principal Investigator will support business development and community engagement efforts, including attending sponsor meetings, conducting physician outreach, attending community education events, engaging in media interviews, and others that help build awareness of clinical research. 

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Onsite in San Juan, PR (no capabilities for remote or hybrid work)
Reports to:  Site President
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

The Company

CMRC Headlands is a premier clinical research site conducting Phase II-IV clinical trials in collaboration with global pharmaceutical sponsors. We advance medical innovation while placing patient experience and operational excellence at the heart of our mission. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do. 

Responsibilities:

  • Lead and oversee clinical trials conducted at CMR Center, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Eligible for or active unencumbered license to practice as an MD or DO in Puerto Rico required.
  • Must be board-certified or board-eligible.
  • Bilingual in English and Spanish required
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
  • Experience in obesity, cardiometabolic disease, vaccines, CNS, gastroenterology, rheumatology, nephrology, pediatrics, or other relevant therapeutic areas preferred.
  • Existing patient access, referral network, or community relationships preferred. 

Apply