1

Clinical Trial Transparency Jobs in Indiana (NOW HIRING)

Clinical Trial Transparency information

See Indiana salary details

$27

$59

$91

How much do clinical trial transparency jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical trial transparency in Indiana is $59.49, according to ZipRecruiter salary data. Most workers in this role earn between $48.27 and $67.02 per hour, depending on experience, location, and employer.

What is a clinical trial transparency?

A Clinical Trial Transparency job involves ensuring that information about clinical trials is publicly disclosed in compliance with global regulations and transparency policies. Professionals in this role manage the registration of trials on public databases, oversee the timely reporting of results, and ensure adherence to ethical and legal requirements. They collaborate with regulatory teams, medical writers, and legal departments to promote data accessibility and public trust in clinical research.

What are the main responsibilities in a clinical trial transparency role?

In a Clinical Trial Transparency role, your primary responsibilities include preparing and submitting clinical trial data and documents to public registries, ensuring compliance with global regulations, and responding to transparency-related inquiries from regulatory authorities. You’ll work closely with clinical teams, regulatory affairs, and medical writing staff to gather accurate data and ensure timely disclosures. The role often involves managing multiple projects simultaneously, staying updated on evolving disclosure regulations, and supporting audits or inspections. This position is essential in promoting openness, protecting patient privacy, and maintaining the integrity of clinical research.

What are the key skills and qualifications needed to thrive in a clinical trial transparency position, and why are they important?

Excelling in Clinical Trial Transparency requires a comprehensive understanding of clinical research protocols, regulatory compliance (such as FDA, EMA, and ICMJE requirements), and strong project management abilities. Familiarity with disclosure platforms (e.g., ClinicalTrials.gov, EudraCT), data anonymization tools, and relevant certifications like a GCP (Good Clinical Practice) certificate are highly valuable. Attention to detail, effective communication, and stakeholder management are crucial soft skills for success in this role. These capabilities ensure accurate, timely, and compliant disclosure of trial information, which is critical for regulatory approval and upholding public trust.

What are the most commonly searched types of Clinical Trial Transparency jobs in Indiana? The most popular types of Clinical Trial Transparency jobs in Indiana are:
Infographic showing various Clinical Trial Transparency job openings in Indiana as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $123,736 per year, or $59.5 per hour.

Executive Director, Clinical Data Science

Eisai

Indianapolis, IN • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

We are seeking a visionary leader to shape and drive Clinical Data Science strategy across our global clinical development portfolio. This role ensures the rigorous application of statistical principles and advanced data science methodologies to optimize clinical trial efficiency and accelerate innovation. The Executive Director will spearhead the integration of AI/ML solutions for applications in disease diagnosis, modeling, imaging, genomics, proteomics, and precision medicine. Acting as the primary data science representative to global regulatory authorities, this individual will defend strategies and influence industry standards.

Strategic Leadership:

  • Define and execute Clinical Data Science strategies for clinical studies and development plans across the portfolio.
  • Serve as the primary spokesperson for Data Science at Health Authority meetings, leading preparation of responses and influencing regulatory perspectives.

Innovation & Execution:

  • Drive adoption of cutting-edge AI/ML methodologies for disease modeling, biomarker analysis, and precision medicine.
  • Oversee multiple large-scale, critical data science initiatives, ensuring timely, high-quality deliverables aligned with industry best practices.

Risk Management & Problem Solving:

  • Evaluate analytical options, proactively identify risks, and develop novel solutions to complex challenges.

Thought Leadership & External Engagement:

  • Represent the organization at technical seminars and conferences; build networks with industry experts to advance best practices.

Team Leadership & Development:

  • Manage and mentor a diverse team of data scientists and people managers across geographies.
  • Foster career growth through open dialogue, performance management, and strategic development planning.

Operational Excellence:

  • Ensure GxP compliance in data science programming for clinical trials.
  • Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency.

Executive Communication:

  • Deliver clear, compelling communication of complex data science concepts to internal and external stakeholders with executive presence.

Qualifications

  • Ph.D. in Biostatistics or a Master's Degree in Biostatistics in combination with a Ph.D.in Bioinformatics or related computational sciences.
  • Deep expertise in statistical methods and their application in clinical trials.
  • Minimum 10 years of industry experience in clinical development, including Data Science and Biostatistics.
  • Recognized thought leader in at least one data science discipline (e.g., AI/ML modeling, precision medicine).
  • Proven experience presenting at external forums and influencing regulatory authorities.
  • Strong people leadership experience in a Data Science setting.
  • Prior research experience in neurology, particularly Alzheimer's disease biomarkers (plasma, CSF, imaging), strongly preferred.

Eisai Salary Transparency Language:

The annual base salary range for the Executive Director, Clinical Data Science is from :$273,200-$358,600 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation


Eisai logo

About Eisai

Sourced by ZipRecruiter

Eisai is a global pharmaceutical company (headquartered in Woodcliff Lake, NJ, US), renowned for its innovative research and development in neuroscience and oncology. The primary focus of the company is to provide therapeutic treatments and solutions for diseases like Alzheimer's, cancer, and other neurological disorders. Eisai was founded in Japan in 1941 and has since developed a strong presence across international markets. Eisai's core values center around their philosophy of 'human health care' (hhc), where they aim to make significant and positive contributions to patients and their families' healthcare worldwide.

Company size

1,001 - 5,000 Employees

Headquarters location

Nutley, NJ, US

Year founded

1995

Social media