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Clinical Research Associate Jobs in Puerto Rico (NOW HIRING)

Alivia Health

PR · On-site

The Clinical Case Management Associate is responsible for performing telephonic and face to face contact with patients of Alivia Specialty Pharmacy. He or she will evaluate the health care and ...

Alivia Health

PR · On-site

RESUMEN DEL PUESTO Y RESPONSABILIDADES: El/La Asociado(a) de Manejo Clínico de Casos es responsable de realizar contactos telefónicos y presenciales con pacientes de Alivia Specialty Pharmacy.

DaVita

Registered Nurse

San Juan, PR

Associates Degree in Nursing (A.D.N) from accredited school of nursing required; Bachelor of ... care, clinical research), we can guide you on that journey. We offer programs such as: * THRIVE:

MPOWERHealth

PR

Support clinical leadership in process when correcting behavior - including but not limited to ... associate technicians in training, Mentor will be available to contribute to the Academy, research ...

MPOWERHealth

Mentor, MCA-San Juan, PR

San Juan, PR

Support clinical leadership in process when correcting behavior - including but not limited to ... associate technicians in training, Mentor will be available to contribute to the Academy, research ...

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Clinical Research Associate information

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may be challenging for those without related experience or training.

What are Clinical Research Associates?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

What are some common challenges Clinical Research Associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate 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 Associate jobs in Puerto Rico? For Clinical Research Associate jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Puerto Rico look for? The top searched job categories for Clinical Research Associate jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Clinical Research Associate jobs? Cities in Puerto Rico with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Puerto Rico as of June 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution.
Spanish Bilingual Clinical Research Coordinator

Spanish Bilingual Clinical Research Coordinator

IQVIA

San Juan, PR

$41K - $118K/yr

Part-time

Medical, Life

Posted 16 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

54th of 204 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

Pay

Benefits

Hours and flexibility

Workplace

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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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