Chicago, IL · Remote
$86K - $217K/yr
Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...
Chicago, IL · Remote
$86K - $217K/yr
Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Medrio, Clinpal, Medidata Rave, etc.) required * Understanding of clinical research regulations required * Experience in questionnaire development, database structure, and data management processes
Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus. * In-depth knowledge of clinical trial processes. * In-depth knowledge of ...
Quick apply
Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus. * In-depth knowledge of clinical trial processes. * In-depth knowledge of ...
North Chicago, IL · On-site
$84K/yr
Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus. • In-depth knowledge of clinical trial processes. • In-depth knowledge of ...
North Chicago, IL · On-site
$84K/yr
Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus. • In-depth knowledge of clinical trial processes. • In-depth knowledge of ...
$25.73 - $30.37
0% of jobs
$30.37 - $35.01
0% of jobs
$35.01 - $39.66
7% of jobs
$39.66 - $44.30
16% of jobs
$44.88 is the 25th percentile. Wages below this are outliers.
$44.30 - $48.94
13% of jobs
The median wage is $51.68 / hr.
$48.94 - $53.58
23% of jobs
$57.53 is the 75th percentile. Wages above this are outliers.
$53.58 - $58.22
18% of jobs
$58.22 - $62.86
9% of jobs
$62.86 - $67.50
9% of jobs
$67.50 - $72.14
2% of jobs
$72.14 - $76.78
3% of jobs
$25
$53
$76
A Medidata Rave job typically involves working with Medidata Rave, a widely used electronic data capture (EDC) system in clinical trials. Professionals in this role manage study databases, design case report forms (CRFs), ensure data integrity, and support clinical research teams. Roles may include Rave Study Builder, Data Manager, or Clinical Programmer. Strong knowledge of clinical trial processes, database management, and SQL is often required.
To thrive as a Medidata Rave specialist, you need a solid understanding of Electronic Data Capture (EDC) systems, clinical data management, and regulatory guidelines, typically supported by certifications in Medidata Rave or relevant clinical research fields. Proficiency with the Medidata Rave platform, user administration, and familiarity with tools such as SQL or other database management systems are highly valued. Strong attention to detail, communication, and problem-solving skills help professionals stand out in this role. These qualities ensure accurate data collection, regulatory compliance, and effective collaboration in complex clinical trial environments.
Medidata Rave specialists often encounter challenges such as ensuring data accuracy across multiple sites, managing complex study protocols, and troubleshooting technical issues within the platform. They are responsible for configuring case report forms, supporting site users, and maintaining regulatory compliance, which requires constant vigilance and adaptability. Collaboration with clinical research teams, sponsors, and IT staff is vital to address study-specific needs and resolve problems efficiently. These challenges make the role dynamic but also provide opportunities for continuous learning and professional growth.
$86K - $217K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 10 days ago
8.1
Based on 53 frontline employees who took The Breakroom Quiz
61st of 223 rated it services
IQVIA is seeking experienced Senior Data Team Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. This is a remote/WFH position with all necessary equipment provided.
What You'll Do
Who We're Looking For
Ideal candidates will have....
What IQVIA Offers
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 $86,800.00 - $217,100.00. 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.
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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
