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Senior Data Associate Jobs in Mebane, NC (NOW HIRING)

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to ... Ensures that the rights and well-being of human subjects are protected and confirms data quality ...

Duke University

Research Associate, Senior

Durham, NC · On-site

Senior Research Associate Position in Epitranscriptomics in the Meyer Lab (Duke University) The ... Bioinformatics, computational biology, and large-scale data analysis Choose Duke. Successful ...

Duke University

Research Associate, Senior

Durham, NC · On-site

Senior Research Associate Position in Epitranscriptomics in the Meyer Lab (Duke University) The ... Bioinformatics, computational biology, and large-scale data analysis Choose Duke. Successful ...

IQVIA

Associate Director, Data Analytics

Durham, NC · Remote

The Associate Director of Data Analytics provides technical and people leadership to design, build ... Build and maintain senior client relationships; identify expansion opportunities and translate them ...

Data Bridge Consultants

Senior QA Engineer

Cary, NC

$40/hr

Providing guidance and support to associate and intermediate level QA Engineers. * Leading product ... Recommend test approach, test environment requirements, and data strategies * Provide regular ...

Actalent

Senior Associate Research Scientist

Durham, NC · On-site

$35/hr

Senior Associate Research Scientist This Senior Associate Research Scientist role sits within a ... Perform analytical testing and data analysis using established methods with minimal supervision.

Pwc

Oracle SCM - Senior Associate

Greensboro, NC

$77K - $202K/yr

As a Senior Associate, you will focus on building meaningful client connections and learning how to ... interpret data to inform insights and recommendations, and uphold professional and technical ...

Pwc

Oracle SCM - Senior Associate

Raleigh, NC

$77K - $202K/yr

As a Senior Associate, you will focus on building meaningful client connections and learning how to ... interpret data to inform insights and recommendations, and uphold professional and technical ...

Pwc

GIS Web AI Developer, Senior Associate

Raleigh, NC

$77K - $202K/yr

... geographic data across various fields including urban planning, environmental management, and ... As a Senior Associate, you will build meaningful client connections and learn how to manage and ...

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All JobsData Associate JobsSenior Data Associate JobsSenior Data Associate Jobs in Mebane, NC

Senior Data Associate information

What is a senior data associate?

Senior Data Associates are experienced professionals who manage, analyze, and interpret large datasets to support business decision-making. They are responsible for data cleaning, validation, and organization, as well as designing and implementing data collection processes. Senior Data Associates often collaborate with data scientists, analysts, and other stakeholders to ensure data accuracy and accessibility. Their role typically requires strong analytical skills, attention to detail, and proficiency in data management tools and programming languages such as SQL or Python.

How do senior data associates typically collaborate with cross-functional teams within an organization?

Senior Data Associates often work closely with teams such as engineering, product management, and business analytics to ensure data integrity and support organizational goals. They are responsible for translating business requirements into data solutions, managing data pipelines, and providing actionable insights. Regular communication and collaboration are essential, as they often participate in meetings to discuss project progress, data quality issues, and upcoming analytical needs. This cross-functional interaction not only enhances the impact of their work but also fosters a collaborative, learning-oriented environment.

What are the key skills and qualifications needed to thrive as a senior data associate, and why are they important?

To thrive as a Senior Data Associate, you need expertise in data analysis, data management, and a solid understanding of database systems, often supported by a degree in statistics, computer science, or a related field. Familiarity with tools such as SQL, Python, Excel, and data visualization platforms like Tableau is typically required. Strong attention to detail, problem-solving abilities, and effective communication are crucial soft skills for interpreting data and collaborating with stakeholders. These skills ensure accurate data insights, drive informed business decisions, and facilitate efficient teamwork within data-driven organizations.

What is the difference between Senior Data Associate vs Data Analyst?

AspectSenior Data AssociateData Analyst
Required CredentialsBachelor's degree in data-related field; experience in data managementBachelor's degree in statistics, data science, or related field; analytical skills
Work EnvironmentData teams within corporate or research settings, often supporting data operationsBusiness or research environments analyzing data to inform decisions
Employer & Industry UsageUsed in finance, healthcare, tech companies for data support rolesCommon across industries for data interpretation and reporting

The main difference is that Senior Data Associates focus on managing and supporting data processes, while Data Analysts primarily interpret data to generate insights. Senior Data Associates often handle data quality and operations, whereas Data Analysts focus on analysis and reporting.

What are popular job titles related to Senior Data Associate jobs in Mebane, NC?

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Cities near Mebane, NC with the most Senior Data Associate job openings:

Senior Data Associate jobs near you
Infographic showing various Senior Data Associate job openings in Mebane, NC as of June 2026, with employment types broken down into 76% Full Time, 20% Part Time, 2% Temporary, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution.

Sr Clinical Research Associate

Veranex

Raleigh, NC • On-site

$98K - $140K/yr

Other

Re-posted 22 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
The Veranex Clinical Operations team is a dynamic group of professionals providing regulatory, quality and clinical services for the medical device industry. Our team supports start-ups, mid-sized private companies, and the largest corporations at all stages of the product life cycle. We work across a broad spectrum of technologies and treatment modalities. Our clients develop both next-generation and paradigm-shifting devices. Our product exposure includes implantables, instruments (manual, laser, robotic, etc.), capital equipment, combination products, software as a medical device (SaMD), medical mobile apps, in vitro diagnostics and more
About This Role:
Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and execution of clinical trials to evaluate the safety, effectiveness and performance of medical devices. Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence to the clinical protocol, applicable regulations, and company Standard Operating Procedures (SOPs) governing clinical studies.
Location: Remote, US
What You Will Do:
  • Responsible for ensuring that study investigators and coordinators comply with the study protocol, Good Clinical Practices (GCPs), Code of Federal Regulations (CFRs), and Institutional Review Board (IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions
  • Acts as primary liaison to clinical sites.
  • Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits. Generates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)
  • Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities
  • Ensures that the rights and well-being of human subjects are protected and confirms data quality/integrity by maintaining site compliance, reviewing adverse events and device deficiencies, reviewing data trending/metrics, reviewing audit reports, and implementing corrective actions as necessary
  • Supports maintenance of department SOPs and work instructions
  • Supports investigational device traceability including documentation for forecasting, shipping, receipt, and disposition.
  • Supports and maintains documentation of all clinical research activities in the study trial master file (TMF), e.g., monitoring reports, site correspondence, device inventory information.
  • Drives trial enrollment and identifies and communications potential and actual obstacles to enrollment.
  • Travel requirement: 25-50%

Qualifications:
Required skills:
  • Minimum of 5 years of directly related work experience or equivalent in clinical research, including work on medical device significant risk IDE trials and/or non-significant risk abbreviated IDE trials.
  • Must be able to work autonomously and as a member of a cross-functional team and meet high expectations and tight deadlines. May work on highly visible projects in high-pressure situations
  • Must have working knowledge of Good Clinical Practices (GCPs), FDA regulations and IRB requirements.
  • Must have strong project management competencies and ability to work with high quality, reliability, and attention to detail.
  • Must have a strong level of professionalism, including verbal and written communication skills; and the ability to communicate with all levels of the organization, cross-functionally, and with clients/partners.
  • Must have proficiency in using Microsoft Office Suite, including Word, Excel, Outlook and PowerPoint; as well as experience with electronic data capture (EDC) and electronic Trial Master File (eTMF) systems.
  • Experience interfacing successfully with physicians/clinical staff and familiarity with hospital/clinical environments
  • Familiarity with medical and anatomical terminology.
  • Ability and willingness to travel

Preferred:
  • BS or BA degree preferred; BS or BA in a relevant scientific discipline or related field also preferred.

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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