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Clinical Trial Transparency Associate Jobs in Delaware

Agilent

Clinical Affairs Scientist

Wilmington, DE · On-site +1

$105K - $197K/yr

The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...

CEDENT

Study Start-Up Manager

Wilmington, DE · On-site

Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up ... Ensure the timely submission of documents to regulatory authorities and maintain the trial master ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

AstraZeneca

Clinical Study Administrator

Wilmington, DE · On-site

$93K - $139K/yr

... Associate's degree or an equivalent combination of education and relevant experience will be ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Partner closely with CRAs and the Local Study Team/Local Study Associate Director to achieve start ... of clinical trial process across Phases II-IV and ICH GCP - Good understanding of clinical ...

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All JobsClinical Trial Transparency Associate JobsClinical Trial Transparency Associate Jobs in Delaware

Clinical Trial Transparency Associate information

See Delaware salary details

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

As of Sep 5, 2026, the average hourly pay for clinical trial transparency associate in Delaware is $40.02, according to ZipRecruiter salary data. Most workers in this role earn between $32.26 and $44.04 per hour, depending on experience, location, and employer.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are popular job titles related to Clinical Trial Transparency Associate jobs in Delaware?

For Clinical Trial Transparency Associate jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Transparency Associate jobs in Delaware look for?

The top searched job categories for Clinical Trial Transparency Associate jobs in Delaware are:

What cities in Delaware are hiring for Clinical Trial Transparency Associate jobs?

Cities in Delaware with the most Clinical Trial Transparency Associate job openings:

Clinical Trial Transparency Associate jobs near you

Clinical Trials Manager

Healthcare Degree

Newark, DE • On-site

$67.90 - $216.75/hr

Other

Posted 4 days ago

Job description

Clinical trial managers are responsible for coordinating and overseeing the entire clinical research process, ensuring that studies are conducted safely, ethically, and in compliance with regulatory requirements. They play a critical role in safeguarding the integrity of research and helping bring new treatments to patients.

Typical responsibilities include:

  • Working closely with principal investigators to develop trials that meet objectives.
  • Creating and managing patient recruitment strategies.
  • Drafting study manuals and protocols.
  • Hiring and supervising clinical trial staff.
  • Collecting, interpreting, and reporting data.
  • Implementing changes to the trial structure based on feedback.
  • Composing status reports and compiling final data summaries.
  • Ensuring regulatory compliance at every stage of the trial.

Salary: According to the Bureau of Labor Statistics (May 2023), clinical trial managers earn on average $127,980 per year. 10th percentile: $67,900; 25th percentile: $86,080; 50th percentile (median): $110,680; 75th percentile: $157,640; 90th percentile: $216,750.

Qualifications: A typical career path requires a master’s degree or graduate certificate in clinical trial management or a related health field, along with at least two years of hands‑on experience in clinical trials. Knowledge of ethics, regulatory compliance, and good clinical practice (GCP) is essential. Candidates may also pursue certifications from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA) to enhance career prospects.

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