Clinical Data Manager
Austin, TX · On-site
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong ... Experience with data listings, query management, edit check programming, and coding dictionaries (e ...
Austin, TX · On-site
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong ... Experience with data listings, query management, edit check programming, and coding dictionaries (e ...
Austin, TX · On-site
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong ... Experience with data listings, query management, edit check programming, and coding dictionaries (e ...
King Of Prussia, PA · Hybrid
$143K - $169K/yr
This role reports to the Director, Statistical Programming Lead Work Environment: *** On site ... Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...
King Of Prussia, PA · Hybrid
$143K - $169K/yr
This role reports to the Director, Statistical Programming Lead Work Environment: *** On site ... Proficiency with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python * Proven experience in clinical trial programming and database management * Knowledge ...
Aliso Viejo, CA · On-site
$45 - $48/hr
Medidata RAVE * Oracle Inform * Medidata * Similar EDC systems * Experience with database concepts ... Experience with SQL, SAS, Excel, or programming tools is a plus * BS degree or higher in Biological ...
Aliso Viejo, CA · On-site
$45 - $48/hr
Medidata RAVE * Oracle Inform * Medidata * Similar EDC systems * Experience with database concepts ... Experience with SQL, SAS, Excel, or programming tools is a plus * BS degree or higher in Biological ...
Boston, MA · On-site
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Boston, MA · On-site
Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM). * Demonstrated experience supporting regulatory submissions is a ...
Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics ... Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ...
Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics ... Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ...
San Francisco, CA · Remote
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Quick apply
San Francisco, CA · Remote
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
San Francisco, CA · On-site +1
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
Quick apply
San Francisco, CA · On-site +1
$1K - $1K/wk
Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , Benchling , and LabArchives . * Design multi-step tasks grounded in your real workflows. Require navigating ...
New
OR · On-site
Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics ... Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ...
OR · On-site
Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics ... Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
New York, NY · On-site
$220K - $250K/yr
Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures ... Provide proactive input into clinical protocol design to ensure data collection strategies align ...
New York, NY · On-site
$220K - $250K/yr
Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures ... Provide proactive input into clinical protocol design to ensure data collection strategies align ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
OR · On-site
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
OR · On-site
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
Cincinnati, OH · On-site
$90K - $120K/yr
Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design ... Apply knowledge of clinical research methods to support various clinical trials and research ...
Cincinnati, OH · On-site
$90K - $120K/yr
Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design ... Apply knowledge of clinical research methods to support various clinical trials and research ...
Cincinnati, OH · Remote
$90K - $120K/yr
... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...
Cincinnati, OH · Remote
$90K - $120K/yr
... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...
Bothell, WA · On-site
$115K - $150K/yr
Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.
Bothell, WA · On-site
$115K - $150K/yr
Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
High School degree and 9+ years of experience in Clinical Programming Preferred Qualifications * 3+ years of experience with Medidata RAVE including database build, edit check programming, data ...
Proficiency in at least one Electronic Data Capture (EDC) system ( Medidata Rave, Veeva Vault EDC ... Knowledge of SQL or other programming languages for data manipulation is a plus. Seniority level ...
Proficiency in at least one Electronic Data Capture (EDC) system ( Medidata Rave, Veeva Vault EDC ... Knowledge of SQL or other programming languages for data manipulation is a plus. Seniority level ...
Atlanta, GA · On-site
Experience with EDC systems (e.g., Medidata Rave, Oracle InForm) Familiarity with TMF structure and regulatory filing practices Understanding of GCP, GCDMP, and clinical trial workflows
Atlanta, GA · On-site
Experience with EDC systems (e.g., Medidata Rave, Oracle InForm) Familiarity with TMF structure and regulatory filing practices Understanding of GCP, GCDMP, and clinical trial workflows
We are seeking a Clinical Analytics Platform Developer to support and configure a global life ... Medidata Rave * Experience executing controlled changes under formal change management and ...
We are seeking a Clinical Analytics Platform Developer to support and configure a global life ... Medidata Rave * Experience executing controlled changes under formal change management and ...
$24.76 - $31.84
3% of jobs
$31.84 - $38.92
4% of jobs
$38.92 - $46
9% of jobs
$46 - $53.08
5% of jobs
$54.30 is the 25th percentile. Wages below this are outliers.
$53.08 - $60.16
17% of jobs
The median wage is $63.26 / hr.
$60.16 - $67.24
25% of jobs
$71.78 is the 75th percentile. Wages above this are outliers.
$67.24 - $74.32
17% of jobs
$74.32 - $81.40
9% of jobs
$81.40 - $88.48
6% of jobs
$88.48 - $95.56
2% of jobs
$95.56 - $102.64
1% of jobs
$24
$64
$102
Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Clinical Data Manager
The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution. Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol. Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams. Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations. Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). Serve as the primary point of contact for data management vendors and oversee their deliverables. Participate in study team meetings and provide status updates related to data quality and timelines. Support audit readiness and participate in regulatory inspections when required.
Bachelor's degree in Life Sciences, Computer Science, Health Informatics, or related field. Minimum of 3–5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment. Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug). Excellent organizational, analytical, and problem-solving skills. Strong communication and collaboration skills across cross-functional teams.
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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Scientific research and development services
51 - 200 Employees
South Plainfield, NJ, US