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Clinical Research Project Assistant Jobs in Puerto Rico

PR · On-site

$18 - $31/hr

... research project -Present research findings at appropriate regional and national professional ... Clinical Sciences and Pharmacy External Basic Qualifications * Doctor of Pharmacy degree from a ...

Oversee and assist Engineers with their assigned projects. * Support the execution activities of ... Collaborate extensively with research, manufacturing, maintenance, process development, utilities ...

... * Assist in the scientific training for Commercial and other internal colleagues regarding ... Clear understanding of clinical research methodologies and ability to independently evaluate and ...

... objectives. - Assist in technical, financial, and organizational issues by researching issues, providing recommendations and maintaining document archives. - Manage and track project budget(s ...

... objectives. * Assist in technical, financial, and organizational issues by researching issues, providing recommendations and maintaining document archives. * Manage and track project budget(s)

... objectives. * Assist in technical, financial, and organizational issues by researching issues, providing recommendations and maintaining document archives. * Manage and track project budget(s)

Administrative Assistant

San Juan, PR · On-site

$17.75 - $23.75/hr

... Assist with research, planning, and coordination of team events • Assist with planning and ... agencies PMO activities: • Enter/review team members' expense reports Other: Assist with ...

Administrative Assistant

San Juan, PR · On-site

$17.75 - $23.75/hr

... Assist with research, planning, and coordination of team events • Assist with planning and ... agencies PMO activities: • Enter/review team members' expense reports Other: Assist with ...

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Showing results 1-20

Clinical Research Project Assistant information

What is the difference between Clinical Research Project Assistant vs Clinical Research Coordinator?

AspectClinical Research Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCR are common
Work EnvironmentSupports research teams in clinical settings, hospitals, or research institutionsManages daily clinical trial activities, interacts directly with patients and investigators
Employer & Industry UsageUsed by research institutions, hospitals, pharmaceutical companiesCommonly employed in clinical trial sites, hospitals, and research organizations

The Clinical Research Project Assistant primarily supports research activities and data management, while the Clinical Research Coordinator oversees trial operations and patient interactions. Both roles require similar educational backgrounds and certifications, but their responsibilities differ in scope and daily tasks.

What job categories do people searching Clinical Research Project Assistant jobs in Puerto Rico look for? The top searched job categories for Clinical Research Project Assistant jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Clinical Research Project Assistant jobs? Cities in Puerto Rico with the most Clinical Research Project Assistant job openings:
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