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Clinical Trial Transparency Associate Jobs in Raleigh, NC

IQVIA

Clinical Research Associate

Durham, NC · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... In this role, you will be responsible for overseeing clinical trial sites to ensure studies are ...

IQVIA, Inc.

Site Monitoring Lead

Durham, NC · On-site

... Clinical Trial Managers (CT Manager) and Clinical Research Associates (CRA). • Participate in development of trial level documents. • Behave as expert and consultant on Site management and ...

IQVIA

Site Monitoring Lead

Durham, NC · On-site

Develop and provide appropriate training of trial monitoring topics to Clinical Trial Managers (CT Manager) and Clinical Research Associates (CRA). Participate in development of trial level documents.

Agilent

Clinical Affairs Scientist

Durham, NC · 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 ...

IQVIA

Site Monitoring Lead

Durham, NC

Develop and provide appropriate training of trial monitoring topics to Clinical Trial Managers (CT Manager) and Clinical Research Associates (CRA). Participate in development of trial level documents.

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

Our associates are involved in every stage of diagnostics, from ideation to development and ... This role is responsible for clinical trial strategies within the US and EU regions for Danaher ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

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Clinical Trial Transparency Associate information

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

As of Sep 10, 2026, the average hourly pay for clinical trial transparency associate in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 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 the most commonly searched types of Clinical Trial Transparency jobs in Raleigh, NC?

The most popular types of Clinical Trial Transparency jobs in Raleigh, NC are:

What are popular job titles related to Clinical Trial Transparency Associate jobs in Raleigh, NC?

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

What job categories do people searching Clinical Trial Transparency Associate jobs in Raleigh, NC look for?

The top searched job categories for Clinical Trial Transparency Associate jobs in Raleigh, NC are:

Clinical Trial Transparency Associate jobs near you

Clinical Research Coordinator - Durham, NC

Durham, NC • On-site

Medix
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Medixexternal

$27 - $30/hr

Full-time

Re-posted yesterday

Key responsibilities

  • Manage and conduct clinical trials from study startup through site closeout, including protocol implementation, vendor management, and subject recruitment.

  • Perform clinical procedures such as phlebotomy, IV/IM dose preparation and administration, fibroscans, ECGs, and vital signs, and collect and process laboratory specimens.

  • Ensure data integrity and regulatory compliance by applying ALCOA-C principles, preparing regulatory documentation, and monitoring adverse events.

Job description

Clinical Research Coordinator
Location: Onsite in Durham, NC
Schedule: Full-Time | Monday - Friday (Regular Schedule)
Employment Type: Contract
Position Overview
Medix is seeking a detail-oriented, highly skilled Clinical Research Coordinator (CRC) to manage and conduct clinical trials from study startup through site closeout.
Operating under Good Clinical Practice (GCP), ICH Guidelines, ALCOA-C principles, and organizational SOPs, this role combines end-to-end trial coordination, regulatory oversight, data integrity, project management, and direct patient care. The CRC serves as a central operational liaison between trial participants, site leadership, sponsors, CROs, vendors, and regulatory bodies.
Key Responsibilities
Clinical Trial Operations & Protocol Management
  • Implement and manage assigned protocols across the full study lifecycle, including study startup, vendor management, subject recruitment, protocol training, source development review, visit scheduling, and study closeout reporting.
  • Evaluate and prescreen potential study subjects via phone and in person; participate in the Informed Consent Form (ICF) process per protocol, local regulations, and IRB standards.
  • Develop, coordinate, and execute operational, research, and administrative strategies to manage assigned protocols effectively while incorporating key timelines, endpoints, vendors, and target patient populations.
  • Apply project management concepts to assess risk, elevate study quality, and align trial operations with organizational financial performance and stakeholder value.
  • Maintain a comprehensive understanding of the product development lifecycle, protocol design, critical data points, and disease processes under study.

Direct Patient Care & Clinical Procedures
  • Perform hands-on clinical duties within licensed scope, including phlebotomy (venipuncture and capillary puncture), intravenous/intramuscular (IV/IM) dose preparation and administration, fibroscans, ECGs, and vital signs.
  • Collect, process, package, and ship laboratory specimens in accordance with study protocols, local laws, and IATA regulations.
  • Promote respect for cultural diversity and conventions in all interactions with subjects, coworkers, and trial partners.

Regulatory Compliance & Data Integrity
  • Ensure strict data integrity by applying ALCOA-C principles when collecting, correcting, and transferring data into sponsor/CRO data capture systems and resolving EDC queries in a timely manner.
  • Prepare, collect, and submit regulatory documentation to Sponsors, CROs, and IRBs per GCP/ICH guidelines and Clinical Trial Agreements.
  • Monitor, document, and escalate Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs), and protocol deviations in accordance with protocols and Eximia SOPs.
  • Develop Quality Control (QC) strategies, communication/escalation workflows, and training tools to prepare for and participate in site audits and inspections.
  • Safeguard participant Protected Health Information (PHI) and protect confidential information across the study team.

Qualifications & Requirements
Education & Experience Options
  • Bachelor's Degree with 1+ years of experience as a Clinical Research Coordinator, OR
  • Associate Degree with 3+ years of experience as a Clinical Research Coordinator, OR
  • High School Diploma / Technical Degree with 5+ years of experience as a Clinical Research Coordinator.

Required Licenses & Certifications
  • Active Phlebotomy certification (where applicable and required by state law).
  • Intravenous (IV) / Intramuscular (IM) dose administration and preparation certification (where applicable and required by state law).
  • Certified Clinical Research Coordinator (CCRC) certification through ACRP or SOCRA (required within 6 months of employment).

Preferred Skills & Competencies
  • Domain Knowledge: Advanced knowledge of medical terminology, protocol design, and specimen processing standards.
  • Technical Skills: Proficient in clinical trial software/EDC systems, Microsoft Office Suite, and standard office hardware.
  • Operational Leadership: Proven ability to work independently, manage multiple deliverables, adapt to rapidly changing daily schedules, and develop team members.
  • Core Strengths: Excellent verbal, written, and interpersonal communication skills; highly organized, detail-oriented, and proficient in strategic problem-solving.

* We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).
* As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
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About Medix Staffing Solutions

Sourced by ZipRecruiter

Since 2001, we’ve been dedicated to helping you achieve your goals. Medix was created to become a leading provider of workforce solutions for clients and candidates across the healthcare and life sciences industries. Today, we are that leader. Headquartered in Chicago, we have 23 offices across the United States, and staff talent around the world. Medix is committed to fulfilling our core purpose as an organization: to positively impact the lives of our talent, clients, and teammates through employment, philanthropy, and opportunity. The combination of purpose and values has nurtured our thriving culture that encourages our internal team to excel at work and in everyday life.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Chicago, IL, US

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