San Juan, PR · On-site
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
San Juan, PR · On-site
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
San Juan, PR · On-site
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
San Juan, PR · On-site
$41K - $118K/yr
On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
This is not a regular Full Time or regular Part Time position; it is a Casual On-Call position. All ... Visually inspect applicants and their belongings prior to allowing entry into the facility. During ...
This is not a regular Full Time or regular Part Time position; it is a Casual On-Call position. All ... Visually inspect applicants and their belongings prior to allowing entry into the facility. During ...
San Juan, PR · On-site
$17.75/hr
This is not a regular Full Time or regular Part Time position; it is a Casual On-Call position. All ... Visually inspect applicants and their belongings prior to allowing entry into the facility. During ...
San Juan, PR · On-site
$17.75/hr
This is not a regular Full Time or regular Part Time position; it is a Casual On-Call position. All ... Visually inspect applicants and their belongings prior to allowing entry into the facility. During ...
$10.62 - $12.13
1% of jobs
$12.13 - $13.64
5% of jobs
$13.64 - $15.15
13% of jobs
$15.66 is the 25th percentile. Wages below this are outliers.
$15.15 - $16.67
19% of jobs
The median wage is $17.67 / hr.
$16.67 - $18.18
19% of jobs
$18.18 - $19.69
15% of jobs
$20.36 is the 75th percentile. Wages above this are outliers.
$19.69 - $21.20
9% of jobs
$21.20 - $22.71
8% of jobs
$22.71 - $24.22
6% of jobs
$24.22 - $25.73
3% of jobs
$25.73 - $27.24
2% of jobs
$10
$18
$27
A Part Time Data Entry job involves inputting, updating, and maintaining data in computer systems or databases. Responsibilities may include typing information from documents, verifying accuracy, and organizing records. These jobs are typically flexible, allowing individuals to work limited hours based on employer needs. They are commonly found in industries like healthcare, finance, retail, and administration. Basic computer skills, attention to detail, and typing proficiency are usually required.
As a Part Time Data Entry professional, your daily tasks typically include entering and updating information into databases or spreadsheets, verifying the accuracy of data, and organizing digital files. You may also be responsible for cross-referencing data sources, flagging discrepancies, and sometimes scanning documents to digitize paper records. Depending on the employer, you might collaborate with other team members or departments to clarify information or retrieve missing data. Attention to detail and consistent workflow are crucial, as your work directly supports accurate business operations.
To thrive as a Part Time Data Entry professional, you need strong attention to detail, fast and accurate typing skills, and at least a high school diploma or equivalent. Familiarity with spreadsheet software (like Microsoft Excel or Google Sheets), database management systems, and sometimes experience with industry-specific platforms is beneficial. Dependability, time management, and the ability to work independently or with minimal supervision are valuable soft skills in this role. These competencies ensure data integrity, efficient workflow, and reliable support for broader organizational operations.
$41K - $118K/yr
Part-time
Medical, Life
Posted 5 days ago
8.1
Based on 53 frontline employees who took The Breakroom Quiz
61st of 230 rated it services
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.
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.
Health care and social assistance
10,000+ Employees
Durham, NC, US
