Job Description
Company Overview
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. With a presence in more than 100 countries, IQVIA partners with pharmaceutical, biotech, and medical device companies to accelerate the development of innovative therapies. The company’s remote workforce enables collaboration across borders while maintaining the highest standards of data integrity and regulatory compliance.
Key Responsibilities
- Accurately enter clinical trial data from source documents into IQVIA’s electronic data capture (EDC) systems, ensuring completeness and adherence to study protocols.
- Perform source data verification (SDV) and resolve discrepancies by liaising with clinical sites, study coordinators, and internal project teams.
- Conduct routine data quality checks, generate query reports, and track query resolution status.
- Maintain detailed audit trails and documentation to support regulatory submissions and inspections.
- Participate in virtual team meetings, provide status updates, and contribute to continuous‑improvement initiatives for data entry processes.
- Follow all data security, privacy, and compliance policies, including HIPAA and GCP guidelines.
Required Qualifications
- High school diploma or equivalent; associate’s or bachelor’s degree in health information, life sciences, or related field preferred.
- Minimum of 2 years of experience in clinical data entry, medical records, or health information management.
- Proficiency with electronic data capture (EDC) systems such as Medidata Rave, Oracle Clinical, or similar platforms.
- Strong attention to detail, excellent typing speed (≥70 wpm) with high accuracy, and ability to manage large volumes of data.
- Familiarity with Good Clinical Practice (GCP), FDA 21 CFR Part 11, and HIPAA regulations.
- Reliable high‑speed internet connection and a dedicated, private workspace for remote work.
Desired Skills
- Experience with data validation tools and query management.
- Knowledge of clinical trial phases and study documentation.
- Ability to work independently while meeting tight deadlines.
- Strong written and verbal communication skills for effective collaboration with global teams.
- Prior experience in a CRO or pharmaceutical environment.
Compensation & Benefits
- Annual base salary range: $58,000 to $78,000, commensurate with experience and location.
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Paid time off, holidays, and flexible work schedule.
- Professional development stipend and access to IQVIA’s learning platform.
- Employee assistance program and wellness resources.
How to Apply
Visit IQVIA’s Careers portal, search for “Remote Clinical Data Entry Associate,” and click “Apply Now.” Upload your current résumé, a cover letter highlighting relevant experience, and any supporting certifications. After submission, a recruiter will review your application and contact you to discuss next steps.
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. With a presence in more than 100 countries, IQVIA partners with pharmaceutical, biotech, and medical device companies to accelerate the development of innovative therapies. The company’s remote workforce enables collaboration across borders while maintaining the highest standards of data integrity and regulatory compliance.
Key Responsibilities
- Accurately enter clinical trial data from source documents into IQVIA’s electronic data capture (EDC) systems, ensuring completeness and adherence to study protocols.
- Perform source data verification (SDV) and resolve discrepancies by liaising with clinical sites, study coordinators, and internal project teams.
- Conduct routine data quality checks, generate query reports, and track query resolution status.
- Maintain detailed audit trails and documentation to support regulatory submissions and inspections.
- Participate in virtual team meetings, provide status updates, and contribute to continuous‑improvement initiatives for data entry processes.
- Follow all data security, privacy, and compliance policies, including HIPAA and GCP guidelines.
Required Qualifications
- High school diploma or equivalent; associate’s or bachelor’s degree in health information, life sciences, or related field preferred.
- Minimum of 2 years of experience in clinical data entry, medical records, or health information management.
- Proficiency with electronic data capture (EDC) systems such as Medidata Rave, Oracle Clinical, or similar platforms.
- Strong attention to detail, excellent typing speed (≥70 wpm) with high accuracy, and ability to manage large volumes of data.
- Familiarity with Good Clinical Practice (GCP), FDA 21 CFR Part 11, and HIPAA regulations.
- Reliable high‑speed internet connection and a dedicated, private workspace for remote work.
Desired Skills
- Experience with data validation tools and query management.
- Knowledge of clinical trial phases and study documentation.
- Ability to work independently while meeting tight deadlines.
- Strong written and verbal communication skills for effective collaboration with global teams.
- Prior experience in a CRO or pharmaceutical environment.
Compensation & Benefits
- Annual base salary range: $58,000 to $78,000, commensurate with experience and location.
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Paid time off, holidays, and flexible work schedule.
- Professional development stipend and access to IQVIA’s learning platform.
- Employee assistance program and wellness resources.
How to Apply
Visit IQVIA’s Careers portal, search for “Remote Clinical Data Entry Associate,” and click “Apply Now.” Upload your current résumé, a cover letter highlighting relevant experience, and any supporting certifications. After submission, a recruiter will review your application and contact you to discuss next steps.
Required Skills
- Clinical
- Data
- Entry