Spanish Bilingual Clinical Research Coordinator Dorado, Puerto Rico
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Job Location:
San Juan, TX - USA
Monthly Salary:
$ 41000 - 118600
Posted on:
17 hours ago
Vacancies:
1 Vacancy
Job Summary
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
Bachelors 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 at
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. 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 $41000.00 - $118600.00. 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.Required Experience:
IC
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
