Spanish Bilingual Clinical Research Coordinator - Dorado, Puerto Rico
IQVIA, San Juan, San Juan, United States
Spanish Bilingual Clinical Research Coordinator - Dorado, Puerto Rico
Work Setup:
On-site
Schedule:
Part-time, 24 hours per week
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 hands‑on role is ideal for a detail‑oriented 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 day‑to‑day 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 hands‑on clinical research coordinating experience.
Demonstrated experience with patient‑facing study visits, EDC data entry and query resolution, patient recruitment and screening, 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 sponsorship.
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, welfare and/or other benefits.
EEO Minorities / Females / Protected Veterans / Disabled.
IQVIA is a proud 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.
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.
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Work Setup:
On-site
Schedule:
Part-time, 24 hours per week
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 hands‑on role is ideal for a detail‑oriented 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 day‑to‑day 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 hands‑on clinical research coordinating experience.
Demonstrated experience with patient‑facing study visits, EDC data entry and query resolution, patient recruitment and screening, 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 sponsorship.
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, welfare and/or other benefits.
EEO Minorities / Females / Protected Veterans / Disabled.
IQVIA is a proud 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.
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.
#J-18808-Ljbffr