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 ...
Sr. Clinical Trials Transparency & Disclosure Specialist
New Haven, CT · On-site
$87K - $114K/yr
The Sr. Clinical Trials Transparency & Disclosure Specialist is responsible for supporting and ... Manage the planning, execution, and oversight of global clinical trial registration and results ...
Sr. Clinical Trials Transparency & Disclosure Specialist
New Haven, CT · On-site
$87K - $114K/yr
The Sr. Clinical Trials Transparency & Disclosure Specialist is responsible for supporting and ... Manage the planning, execution, and oversight of global clinical trial registration and results ...
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 ...
Collaborate withBI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data product ...
Collaborate withBI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data product ...
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 ...
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 Manager
Raleigh, NC · On-site
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager
Raleigh, NC · On-site
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager
Raleigh, NC · On-site +1
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager
Raleigh, NC · On-site +1
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Quick apply
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
The Senior Manager, Clinical Scientist will be instrumental in providing comprehensive clinical trial data reviews, interpreting complex data sets, and creating high-impact scientific content to ...
The Senior Manager, Clinical Scientist will be instrumental in providing comprehensive clinical trial data reviews, interpreting complex data sets, and creating high-impact scientific content to ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data ...
Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Quick apply
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...
Clinical Trial Associate
$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
$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 ...
Sr Clinical Trials Data Coord
Duarte, CA · On-site
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
Sr Clinical Trials Data Coord
Duarte, CA · On-site
Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...
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 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 Aug 12, 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?
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 skills and qualifications are needed for clinical trial data transparency?
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:
Job description
Company Description
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
In collaboration with Trial Statistician, support of Reporting and Analysis Planning (RAP) modules in line with program standards.
Responsible to support development of and implementation of relevant data capture tools in collaboration with CSD, GTL and AQS as documented in data handling plan or equivalent document (e.g. CRFs protocol deviations, questionnaires, diaries, translation, edit checks)
Responsible for performing the ongoing review of clinical trial data as outlined in the data handling plan or equivalent , supports GTL to prepare database lock; and performing data reconciliation along the whole trila duration in collaboration with management.
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 CSD/CSAD, responsible for final analysis and interpretation of results including the development and drafting of clinical trial reports, publications and internal/external presentations.
Provide Support for biomarkers planning and or execution
May serve on or lead global process improvement work streams or act as Subject Matter Experts for training or SOP
May support CSD in limited program level activities
Responsible to support development of and implementation of relevant data capture tools in collaboration with CSD, GTL and AQS as documented in data handling plan or equivalent document (e.g. CRFs protocol deviations, questionnaires, diaries, translation, edit checks)
Responsible for performing the ongoing review of clinical trial data as outlined in the data handling plan or equivalent , supports GTL to prepare database lock; and performing data reconciliation along the whole trila duration in collaboration with management.
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 CSD/CSAD, responsible for final analysis and interpretation of results including the development and drafting of clinical trial reports, publications and internal/external presentations.
Provide Support for biomarkers planning and or execution
May serve on or lead global process improvement work streams or act as Subject Matter Experts for training or SOP
May support CSD in limited program level activities
Qualifications
Skills:
Basic knowledge in planning, executing, reporting and publishing global clinical studies in a pharmaceutical company or contract research organization. Work experience in clinical operations preferable.
Strong interpersonal skills
Ability to work under pressure
Excellent negotiation and conflict resolution skills
Collaborates across boundaries for shared success
Resolve issues with minimal supervision and understand when to escalate
Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
Strong analytical / computational background
Demonstrates excellent Medical / scientific writing skills
Demonstrates knowledge and application of statistical analysis methodology and can identify trends and analyze / interpret / report data effectively
Education:
Advanced degree in life sciences/healthcare (or clinically relevant degree) is required.
PharmD, PhD or MD preferable.
Basic knowledge in planning, executing, reporting and publishing global clinical studies in a pharmaceutical company or contract research organization. Work experience in clinical operations preferable.
Strong interpersonal skills
Ability to work under pressure
Excellent negotiation and conflict resolution skills
Collaborates across boundaries for shared success
Resolve issues with minimal supervision and understand when to escalate
Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
Strong analytical / computational background
Demonstrates excellent Medical / scientific writing skills
Demonstrates knowledge and application of statistical analysis methodology and can identify trends and analyze / interpret / report data effectively
Education:
Advanced degree in life sciences/healthcare (or clinically relevant degree) is required.
PharmD, PhD or MD preferable.
Additional Information
Neha Sharma
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax:Â 973.998.2599
Website: www.artechinfo.com
About Artech
Sourced by ZipRecruiter
Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).
Industry
Recruiting and staffing services
Company size
10,000+ Employees
Headquarters location
Morristown, NJ, US
Year founded
1992