Clinical Data Analyst
Hillsborough, NJ · On-site
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
Clinical Data Analyst
Hillsborough, NJ · On-site
Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...
Senior Clinical Programmer
Cambridge, MA · On-site +1
The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...
Senior Clinical Programmer
Cambridge, MA · On-site +1
The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...
In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide. What ...
In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide. What ...
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Manage clinical trial data sets, ensuring accuracy, consistency, and security. Ensure that all clinical trial data are accurately entered into electronic data capture (EDC) systems and promptly ...
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
Expert Clinical Manager
East Hanover, NJ · On-site
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
Expert Clinical Manager
East Hanover, NJ · On-site
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT) In collaboration with Medical Lead/BSL or ...
With support, liaise with the trial data manager (TDM) and labs for data transfer and data ... At least 2 years of experience handling clinical samples Familiarity with biomarker discovery ...
With support, liaise with the trial data manager (TDM) and labs for data transfer and data ... At least 2 years of experience handling clinical samples Familiarity with biomarker discovery ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Clinical Trial Screening Coordinator The Clinical Trial Screening Coordinator will act as a liaison ... Accountable for coordinating pre-screen data management activities - performing quality checks on ...
Required : • Deep technical expertise in clinical trial data platforms, clinical data architecture, or related healthcare/life sciences data environments. • Experience designing, architecting, or ...
Required : • Deep technical expertise in clinical trial data platforms, clinical data architecture, or related healthcare/life sciences data environments. • Experience designing, architecting, or ...
Clinical Trial Assistant
New York, NY · On-site
$75K - $85K/yr
Track Case Report Forms, data queries, and clinical data flow from submission through resolution ... Coordinate with Clinical Trial Supply vendors and manage tracking systems for investigational ...
Clinical Trial Assistant
New York, NY · On-site
$75K - $85K/yr
Track Case Report Forms, data queries, and clinical data flow from submission through resolution ... Coordinate with Clinical Trial Supply vendors and manage tracking systems for investigational ...
Clinical Data Manager
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Clinical Data Manager
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Clinical Data Manager
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Clinical Data Manager
Somerset, NJ · On-site
$60K - $75K/yr
The Clinical Data Manager ensures the integrity, accuracy, and compliance of clinical trial data, adhering to regulatory requirements, SOPs, and data standards. Responsibilities include overseeing ...
Clinical Trial Manager JOIN US AT CIVIA HEALTH Civia Health operates a nextgeneration SMO model ... Data Quality, and Safety - supported by disciplined governance, transparency, and performance ...
Clinical Trial Manager JOIN US AT CIVIA HEALTH Civia Health operates a nextgeneration SMO model ... Data Quality, and Safety - supported by disciplined governance, transparency, and performance ...
CA · On-site
Strong understanding of clinical trial data lifecycle from data collection through analysis and submission readiness. * Ability to convert clinical requirements into clear technical specifications.
CA · On-site
Strong understanding of clinical trial data lifecycle from data collection through analysis and submission readiness. * Ability to convert clinical requirements into clear technical specifications.
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...
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Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Description The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Description The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial ...
Clinical Trial Associate
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
... data accuracy, consistency, formal quality and readability, resolving identified issues in ... Solid knowledge of clinical trial transparency principles, preferably on an international level ...
Clinical Trial Associate
Woodcliff Lake, NJ · On-site
$35.50 - $48.50/hr
... data accuracy, consistency, formal quality and readability, resolving identified issues in ... Solid knowledge of clinical trial transparency principles, preferably on an international level ...
Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Clinical Trial Associate/Clinical Research Coordinator
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
Conducting reviews of trial data and follow GCP/ICH protocols/guidelines. Will require travel to Clinical sites, including up to 50% of the time, during peak periods. Primary Responsibilities:
Clinical Trial Data Transparency information
See salary details
$13.94 - $20.56
5% of jobs
$20.56 - $27.19
6% of jobs
$29.74 is the 25th percentile. Wages below this are outliers.
$27.19 - $33.81
35% of jobs
The median wage is $34.45 / hr.
$33.81 - $40.43
38% of jobs
$40.43 - $47.05
6% of jobs
$47.05 - $53.67
3% of jobs
$53.67 - $60.29
2% of jobs
$60.29 - $66.91
0% of jobs
$66.91 - $73.54
0% of jobs
$73.54 - $80.16
1% of jobs
$80.16 - $86.78
3% of jobs
$13
$38
$86
How much do clinical trial data transparency jobs pay per hour?
As of Jun 9, 2026, the average hourly pay for clinical trial data transparency in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.
What is a Clinical Trial Data Transparency job?
A Clinical Trial Data Transparency job involves managing the disclosure and sharing of clinical trial data in compliance with regulatory requirements and ethical guidelines. Professionals in this role ensure that trial data is accessible to researchers, healthcare professionals, and the public while protecting patient privacy and proprietary information. Responsibilities may include preparing clinical study reports, redacting sensitive data, and maintaining compliance with global transparency regulations. This role is critical for maintaining trust in clinical research and supporting scientific advancements.
What are the key skills and qualifications needed to thrive in the Clinical Trial Data Transparency position, and why are they important?
To thrive in Clinical Trial Data Transparency, you need a strong background in clinical research, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with data anonymization tools, CTIS (Clinical Trial Information System), CDISC standards, and regulations such as EMA Policy 0070 or FDA requirements is valuable. Excellent attention to detail, communication skills, and a collaborative mindset help ensure accurate and effective data sharing. These skills and qualities are vital for ensuring transparent, compliant, and responsible dissemination of clinical trial data while protecting patient privacy.
What are some typical challenges faced in a Clinical Trial Data Transparency role?
Professionals in Clinical Trial Data Transparency often navigate complex regulatory requirements and tight deadlines to ensure timely data disclosure while safeguarding participant confidentiality. You may face challenges related to interpreting evolving global regulations, coordinating across international teams, and handling large volumes of sensitive data. Collaboration with legal, regulatory, and data management teams is common, so strong communication and organizational skills are essential. By effectively managing these challenges, you play a crucial role in upholding ethical standards and public trust in clinical research.
More about Clinical Trial Data Transparency jobs
What cities are hiring for Clinical Trial Data Transparency jobs? Cities with the most Clinical Trial Data Transparency job openings:
What are the most commonly searched types of Clinical Trial Data Transparency jobs? The most popular types of Clinical Trial Data Transparency jobs are:
What job categories do people searching Clinical Trial Data Transparency jobs look for? The top searched job categories for Clinical Trial Data Transparency jobs are:
- Clinical Research Associate 1099
- Clinical Research Director
- Clinical Research Site Manager
- History Research Assistant
- Full Time Davita Clinical Research
- Clinical Research Data Assistant
- Volunteer Icon Clinical Research
- Clinical Research Associate
- Seasonal Senior Clinical Research Associate
- International Clinical Research Nurse
Full-time
Posted 15 days ago
Job description
R3 Technology Inc. seeks Clinical Data Analyst for it Hillsborough NJ office. Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory, pharmacology and immunology. May travel and relocate to various unanticipated sites within the United States. Must have Master's degree in Bio-Informatics, Biology, Health Services Administration or related field.
Send resumes and cover letter to hr@r3tek.com . Clearly reference position. NO CALLS. EOE.
Send resumes and cover letter to hr@r3tek.com . Clearly reference position. NO CALLS. EOE.
About R3TEK
Sourced by ZipRecruiter
Industry
It services
Company size
51 - 200 Employees
Headquarters location
Hillsborough, NJ, US
Year founded
2006