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Full Time Clinical Trial Data Transparency Jobs (NOW HIRING)

Clinical Trial Manager

Raleigh, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... full-time position is $86,000 - $105,000. Ardelyx utilizes industry data to ensure that our ...

Clinical Trial Manager

Raleigh, NC · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Clinical Trial Manager

Philadelphia, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... full-time position is $86,000 - $105,000. Ardelyx utilizes industry data to ensure that our ...

Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... full-time position is $86,000 - $105,000. Ardelyx utilizes industry data to ensure that our ...

Showing results 21-40

Full Time Clinical Trial Data Transparency information

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$13

$38

$86

How much do full time clinical trial data transparency jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for full time 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 are the most commonly searched types of Clinical Trial Data Transparency jobs?

The most popular types of Clinical Trial Data Transparency jobs are:

Full-time

Re-posted 26 days ago


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

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

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.


Additional Information

Neha Sharma
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax:  973.998.2599
Website: www.artechinfo.com




Artech logo

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