ZipRecruiter

Log In

1

Clinical Trial Data Transparency Jobs (NOW HIRING)

Pharmaron

Clinical Data Manager

Somerset, NJ

$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 ...

Civia Health

Clinical Trial Manager

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 ...

Pharmaron

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 ...

Viking Therapeutics

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 ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

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 ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... This includes vendor management, monitoring subject safety and data collection, and ensuring ...

asrcfh

Clinical Data Manager

Reston, VA

Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and procedures * Process, track, and validate data accurately and on time, in ...

asrcfh

Clinical Data Manager 2

Reston, VA · On-site

Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and procedures * Process, track, and validate data accurately and on time, in ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...

next page

Showing results 1-20

All JobsClinical Trial Data Transparency Jobs

Clinical Trial Data Transparency information

See salary details

$13

$38

$86

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

As of Jul 5, 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 Trial Data Transparency jobs near you
Infographic showing various Clinical Trial Data Transparency job openings in the United States as of June 2026, with employment types broken down into 44% Full Time, 46% Part Time, and 10% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Clinical Trial Screening Coordinator

Clinical Trial Screening Coordinator

DM Clinical Research

Tomball, TX

Full-time

Posted 4 days ago

Job description

Clinical Trial Screening Coordinator
The Clinical Trial Screening Coordinator will act as a liaison between the recruitment and clinical trials teams to ensure that potential trial subjects are assigned to the trial best suited for them. To ensure that subjects have the required paperwork, medical records, and authorizations to participate in trials. To demonstrate effective knowledge of protocols, including inclusion/exclusion criteria. To demonstrate knowledge of Good Clinical Practices and FDA regulations specifically pertaining to the recruitment and retention of study subjects.
  • DUTIES amp; RESPONSIBILITIES
  • Completing DMCR-required training, including GCP and NIH.
  • Ensuring all patient enrollment activities are performed as per clinical trial protocol parameters by engaging directly with the CRCs and working closely with the clinical trial team.
  • Interfacing with potential research subjects to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent and coordinate appointments with the recruitment team.
  • Managing pre-screen operational activities and establishing strong relationships with clinical trial sites and the staff.
  • Accountable for coordinating pre-screen data management activities - performing quality checks on timely data entry and data quality in the clinical research electronic system (CRIO).
  • Ensuring availability of study participant's information by accurately filing and/or retrieving study participant records as requested by management
  • Being prepared for and available at all required company meetings.
  • Submitting administrative paperwork per company timelines.
  • Any other matters as assigned by management.
KNOWLEDGE amp; EXPERIENCE
Education:
  • FMG (Foreign Medical Graduate) preferred or
  • Bachelors in Health Care Sciences or
  • Nursing Degree- LVN, LPN, or RN
Experience:
  • 3-4 years of Medical terminology
  • 1-2 years of customer service experience
  • 1-2 years of clinical research experience preferred
Credentials:
  • N/A
Knowledge and Skills:
  • Dependability
  • Medical Spanish a plus
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have attention to detail and accuracy.
  • Extreme attention to detail (strict adherence to procedures and protocols is essential)
  • Good knowledge of Good Clinical Practices and FDA regulations, protocols
  • Ability to use computer applications for data capture and for general communication required to
  • Communicate effectively, both orally and in writing

Apply