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Clinical Trial Transparency Associate Jobs in Delaware

AstraZeneca

Local Study Associate Director

Wilmington, DE · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a Local Study Associate Director, you will lead cross-functional Local Study Teams to deliver ... clinical trial transparency are accurate and up to date. * Monitoring Oversight and Quality:

New

CEDENT

Study Start-Up Manager

Wilmington, DE

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

CRA Manager

Wilmington, DE · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Clinical Research Associates to deliver robust site performance, first-time quality, and on-time ... Lead special initiatives that improve trial execution, standardize practices, and scale learnings ...

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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 Aug 15, 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 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 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 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 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 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

Local Study Associate Director

AstraZeneca

Wilmington, DE • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Are you ready to lead country execution of pivotal clinical studies and help bring new cancer medicines to patients faster? This is your opportunity to turn global study designs into high-quality local delivery that accelerates recruitment, safeguards data integrity, and advances the standard of care! As a Local Study Associate Director, you will lead cross-functional Local Study Teams to deliver country commitments on time, to budget and quality, and always in line with ICH-GCP and local regulations. You will translate strategy into action, balancing speed with rigor, and removing barriers so investigators and sites can focus on patients. How will you shape country plans that drive performance and elevate quality? You will own end-to-end oversight of country activities-from feasibility and site selection through start-up, monitoring, and close-out-while working closely with global counterparts and local partners. In a science-led, collaborative environment, you will be empowered to anticipate risks, make clear decisions, and continuously improve how we operate at pace.
Accountabilities:
  • Country Study Leadership: Own delivery of country commitments, ensuring data quality, adherence to timelines, and budget discipline.
  • Local Study Team Management: Lead and optimize performance of CRAs and CSAs, fostering a high-trust, high-performance environment with clear goals and feedback.
  • Feasibility and Site Selection: Drive robust country and site feasibility; identify potential investigators, conduct Site Quality Risk Assessments and Site Qualification Visits to select high-performing sites.
  • Start-up and Regulatory Interface: Ensure timely, high-quality submissions to Ethics Committees/IRBs and Regulatory Authorities in partnership with Regulatory Affairs for study start-up and throughout the study.
  • Budget and Contracts: Prepare and own the country financial Study Management Agreement (fSMA); maintain accurate study budgets and financial records; lead preparation of local Master CSA (including site budgets) and amendments as needed.
  • Informed Consent and Essential Documents: Prepare country-level Master Informed Consent Form and site ICFs, including translations; verify collection and correctness of all essential documents before site activation.
  • Drug Supply and Local Logistics: Plan and coordinate local drug activities from procurement or reimbursement through to destruction in line with study needs and local requirements.
  • Systems and Transparency: Set up and maintain studies in CTMS and any required local systems; ensure critical systems enabling safety reporting, regulatory submissions and clinical trial transparency are accurate and up to date.
  • Monitoring Oversight and Quality: Oversee monitoring from activation through closure in accordance with monitoring plans; review monitoring reports; conduct co-monitoring and accompanied visits; step in to perform site monitoring as needed to support flexible capacity.
  • Risk Management and Issue Resolution: Develop and maintain the country risk management plan; proactively identify, mitigate and resolve risks, issues, and deviations across sites and vendors.
  • Stakeholder Engagement and Recruitment: Lead interactions with investigators, site staff, and national coordinators; shape and implement patient recruitment strategies; plan and lead national investigator meetings in line with local codes.
  • Forecasting and Resource Planning: Support forecasting of timelines, resources, recruitment, budget, study materials, and drug supply to secure delivery.
  • Training and Coaching: Train and mentor new team members; provide performance insights on CRAs/CSAs to line management; build study capability and consistency.
  • Audit/Inspection Readiness and eTMF: Keep the eTMF inspection-ready with timely, complete document upload; lead audit and inspection activities with QA partners; ensure readiness for final archiving.
  • Compliance and Ethics: Uphold ICH-GCP, AZ Procedural Documents, local regulations, codes of ethics, and all company policies across people, finance, technology, security and SHE.
  • Collaboration and Reporting: Build strong relationships with global study leadership and local Medical Affairs; provide clear, consistent study updates and insights to business partners.
  • Continuous Improvement: Contribute to process improvements and SMM initiatives at local, regional, and global levels to enhance efficiency and quality.

Essential Skills/Experience:
  • BS in related field, preferably in life science, or equivalent
  • Minimum 3 years of experience in Development Operations (CRA, SrCRA) or other related fields (Medical Affairs-led or Academic-led studies).
  • Strong understanding of international guidelines ICH GCP as well as relevant local regulations.
  • Proven track record leading and motivating cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality.
  • Project management skills.
  • Team building and interpersonal skills.
  • Organizational skills.
  • Verbal and written communication skills.
  • Ability to prioritize and handle multiple tasks.
  • Attention to details.
  • Negotiation skills.
  • Ability to learn and to adapt to work with IT systems.
  • Ability to travel nationally and internationally as required.

Desirable Skills/Experience:
  • Medical knowledge and ability to learn relevant AZ Therapeutic Areas.
  • Knowledge of the Drug Development Process.
  • Understanding of the Clinical Study Process including monitoring.
  • Understanding of the Study Drug Handling Process and the Data Management Process.
  • Integrity and high ethical standards.
  • Analytical skills.
  • Resource management skills.
  • Decision making and delegation skills.
  • Financial leadership skills.
  • Change management skills.
  • Coaching skills.
  • Ability in handling crisis situations.
  • Intercultural awareness.

The annual base pay for this position ranges from $137,937.60 - $206,906.40. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.
When we put unexpected teams in the same room, we ignite ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca: Here, science leads and curiosity never stops-teams are trusted to push boundaries, fuse innovative technology with deep clinical expertise, and turn bold ideas into medicines that change clinical practice. With a strong track record of delivering new cancer therapies across multiple indications, significant ongoing investment in R&D, and close partnerships with leading academic centers, you will join a community that publishes at the highest levels and learns fast together. We value kindness alongside ambition, empowering leaders at every level to ask questions, take smart risks and collaborate across fields to make a tangible difference for patients facing some of the hardest-to-treat diseases.
Step into a role where your country leadership will accelerate breakthrough studies and improve patients' lives-make your move and shape what comes next today.
Date Posted
12-Aug-2026
Closing Date
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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