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Clinical Data Management Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Lead Clinical Data Manager (Remote)

Durham, NC · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Lead Clinical Data Manager (Remote)

Raleigh, NC · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Clinical Data Strategist

Durham, NC

$86K - $216K/yr

Ensure the data collected and integrated into the Data Factory (DF)/Clinical Data Repository (CDR ... Complete and manage the 'Systems Integration Plan' to detail the data flow and highlight potential ...

IQVIA

Clinical Data Strategist

Durham, NC · On-site

$86K - $216K/yr

Ensure the data collected and integrated into the Data Factory (DF)/Clinical Data Repository (CDR ... Complete and manage the 'Systems Integration Plan' to detail the data flow and highlight potential ...

IQVIA, Inc.

Clinical Data Strategist

Durham, NC · On-site

$86K - $216K/yr

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Experience working in Drug Discovery, clinical trial conduct, clinical data management or related industries. Excellent critical thinking and analytical ...

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Clinical Data Management information

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$79

How much do clinical data management jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for clinical data management in Raleigh, NC is $55.57, according to ZipRecruiter salary data. Most workers in this role earn between $43.94 and $66.11 per hour, depending on experience, location, and employer.

What is the work of clinical data management?

Clinical data management involves collecting, cleaning, and maintaining data generated during clinical trials to ensure accuracy, completeness, and consistency. It includes designing data collection tools, validating data, and managing databases using specialized software, often requiring attention to regulatory standards and good clinical practice. The role is essential for supporting reliable analysis and decision-making in drug development.

What is clinical data management?

Clinical data management (CDM) is a critical process in clinical research that involves collecting, cleaning, and managing data generated during clinical trials. The goal is to ensure that the data is accurate, reliable, and compliant with regulatory standards. CDM professionals work closely with researchers, statisticians, and regulatory bodies to validate data and ensure its integrity throughout the study. This process helps in making informed decisions about the safety and efficacy of new drugs or treatments.

What are some common challenges faced by professionals in Clinical Data Management, and how can they be addressed?

One of the common challenges in Clinical Data Management is ensuring data accuracy and consistency across multiple sources and formats. This often involves resolving discrepancies and managing large volumes of data within tight timelines. Effective communication with clinical research associates, statisticians, and IT teams is crucial to address data queries promptly and maintain data integrity. Staying updated with regulatory requirements and leveraging advanced data management systems can also help mitigate these challenges and improve overall workflow efficiency.

What is the difference between Clinical Data Management vs Clinical Data Coordinator?

AspectClinical Data ManagementClinical Data Coordinator
ResponsibilitiesDesigning data collection processes, database setup, data validation, and ensuring data quality for clinical trials.Collecting, reviewing, and entering clinical trial data, ensuring accuracy and completeness.
Required SkillsKnowledge of data management systems, clinical trial processes, and data validation techniques.Attention to detail, data entry skills, familiarity with clinical trial documentation.
Work EnvironmentTypically in clinical research organizations, pharmaceutical companies, or CROs.Often within clinical sites or research teams supporting data collection activities.

While both roles focus on clinical trial data, Clinical Data Management involves designing and overseeing data systems and ensuring data integrity, whereas Clinical Data Coordinators handle the day-to-day data collection and entry tasks. Both are essential for successful clinical research but differ in scope and responsibilities.

Is clinical data management a good career?

Clinical data management is a vital role in the healthcare and pharmaceutical industries, involving the collection, validation, and analysis of clinical trial data. It requires knowledge of data management tools, regulatory standards, and attention to detail, offering opportunities for career growth and specialization. The field is generally considered stable with increasing demand due to ongoing clinical research activities.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical trials, monitoring, or related roles. Entry-level roles in clinical data management or clinical research may include assistant or coordinator positions, with CRAs often needing a background in life sciences, healthcare, or related certifications. Advancement to CRA roles generally involves gaining experience and developing skills in regulatory compliance and trial monitoring tools.

What are the key skills and qualifications needed to thrive in Clinical Data Management, and why are they important?

To thrive in Clinical Data Management, you need a strong background in life sciences, attention to detail, and understanding of clinical trial processes, often supported by a relevant degree. Familiarity with industry-standard data management systems such as Medidata Rave or Oracle Clinical, as well as knowledge of CDISC standards and regulatory requirements, is essential. Excellent organizational skills, communication, and problem-solving abilities help ensure data integrity and effective cross-functional collaboration. These skills and qualities are crucial for ensuring high-quality, compliant data that supports clinical research and regulatory submissions.

How do I become a Clinical Data Manager?

To become a Clinical Data Manager, typically a bachelor's degree in life sciences, healthcare, or a related field is required. Relevant skills include knowledge of clinical trial processes, data management tools like EDC systems, and attention to detail; certifications such as CDMP can enhance job prospects. Gaining experience through internships or entry-level roles in clinical research is also beneficial.
What are the most commonly searched types of Clinical Data Management jobs in Raleigh, NC? The most popular types of Clinical Data Management jobs in Raleigh, NC are:
What are popular job titles related to Clinical Data Management jobs in Raleigh, NC? For Clinical Data Management jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Data Management jobs in Raleigh, NC look for? The top searched job categories for Clinical Data Management jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Data Management jobs? Cities near Raleigh, NC with the most Clinical Data Management job openings:
Clinical Data Management jobs near you
Infographic showing various Clinical Data Management job openings in Raleigh, NC as of June 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $115,589 per year, or $55.6 per hour.
Lead Clinical Data Manager

Lead Clinical Data Manager

Katalyst Healthcares & Life Sciences

Durham, NC • On-site

Other

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

Job description

Clinical Data Manager

Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards.

Provide strategic oversight and direction to CRO clinical data management teams for assigned studies.

Develop and implement data management plans, case report forms (CRFs), edit checks, and data validation plans in alignment with study protocols and regulatory requirements.

Oversee the design, build, and validation of clinical databases using Medidata Rave EDC, ensuring optimal configuration and functionality.

Conduct thorough reviews of clinical data, identifying trends, inconsistencies, and potential issues that may impact data quality or study outcomes.

Collaborate with cross-functional teams including Biostatistics, Clinical Operations, Safety, and Regulatory to ensure alignment of data management strategies with overall clinical development goals.

Provide oversight, and performance management of external data management vendors.

Maintain SOPs, guidelines, and best practices for clinical data management processes.

Represent the Clinical Data Management function in internal and external meetings, providing expert guidance on data-related matters.

Stay current with industry trends, regulatory requirements, and technological advancements in clinical data management, particularly in the oncology field.

Bachelor's degree in Life Sciences, Computer Science, or a related field; advanced degree preferred.

A minimum of 7+ years of clinical data management experience in the biotechnology or pharmaceutical industry.

Experience managing oncology clinical trials data, including a deep understanding of oncology-specific data requirements and challenges.

Expert-level proficiency with Medidata Rave EDC, including system configuration, form design, and edit check programming.

Strong knowledge of clinical research processes, FDA & ICH guidelines, GCP, GCDMP, and CDISC standards.

Demonstrated experience in CRO and vendor oversight.

Excellent project management skills with the ability to manage multiple studies simultaneously.

Strong analytical and problem-solving skills with meticulous attention to detail.

Outstanding communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders.

Proficiency in Microsoft Office Suite and familiarity with statistical software (e.g., SAS, R) is a plus.

CCDM (Certified Clinical Data Manager) certification

Experience with risk-based monitoring in oncology studies

Knowledge of emerging technologies in clinical data collection and management (e.g., ePRO, wearables, AI/ML applications)

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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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