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Clinical Data Manager Ii Jobs in Raleigh, NC (NOW HIRING)

Fortrea

Associate Clinical Data Manager

Durham, NC · On-site

Data Management leadership on studies and take responsibility for the development of the project ... Provides leadership, mentorship, and coaching in DM related clinical trial processes to the ...

Fortrea

Senior Clinical Data Manager

Durham, NC · On-site

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ... with minimum 2 years of direct sponsor management and at least 2 years technical mentoring ...

Fortrea

Sr. Clinical Data Manager

Durham, NC

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring ... with minimum 2 years of direct sponsor management and at least 2 years technical mentoring ...

New

Pharpoint Research

Principal Data Manager

Durham, NC · On-site

Experience: 3 years' related experience and 2 years in clinical data management or related field. * An equivalent combination of education and experience may be accepted as a satisfactory substitute ...

IQVIA

Senior Data Team Lead (Remote)

Raleigh, NC · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

IQVIA

Senior Data Team Lead (Remote)

Durham, NC · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

IQVIA

Lead Data Manager

Durham, NC

$89K - $224K/yr

Minimum 7+ years of Clinical Data Management experience in pharmaceutical, biotechnology, or CRO environments. Strong knowledge of clinical trial processes from study start-up through closeout.

IQVIA

Lead Data Manager

Durham, NC · On-site

$89K - $224K/yr

Minimum 7+ years of Clinical Data Management experience in pharmaceutical, biotechnology, or CRO environments. Strong knowledge of clinical trial processes from study start-up through closeout.

IQVIA, Inc.

Lead Data Manager

Durham, NC · On-site

$89K - $224K/yr

Minimum 7+ years of Clinical Data Management experience in pharmaceutical, biotechnology, or CRO environments. Strong knowledge of clinical trial processes from study start-up through closeout.

IQVIA

Mgr, Database Management Systems

Durham, NC · On-site

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Essential Functions Clinical Data Standards & Operational Mapping * Participate in the development ...

WCPSS

Data Manager

Garner, NC · On-site

AND Two years of experience directly relating to computer systems which require knowledge of editing and completing source data. An equivalent combination of education and relevant experience ...

WCPSS

Data Manager

Garner, NC

AND * Two years of experience directly relating to computer systems which require knowledge of editing and completing source data. An equivalent combination of education and relevant experience ...

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All JobsClinical Data Ii JobsClinical Data Manager Ii JobsClinical Data Manager Ii Jobs in Raleigh, NC

Clinical Data Manager Ii information

See Raleigh, NC salary details

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How much do clinical data manager ii jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical data manager ii 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 skills and qualifications are needed to be a clinical data manager II?

To thrive as a Clinical Data Manager II, you need a solid background in clinical research, data management principles, and a relevant degree such as life sciences or computer science. Experience with electronic data capture (EDC) systems, data query management tools, and industry certifications like CDISC or SCDM are highly valued. Attention to detail, problem-solving, and strong communication skills set outstanding candidates apart in this role. These competencies ensure accurate, efficient data management and regulatory compliance, which are critical for successful clinical trial outcomes.

What is the difference between Clinical Data Manager Ii vs Clinical Data Coordinator?

AspectClinical Data Manager IiClinical Data Coordinator
CredentialsBachelor's degree in life sciences or related field; experience in data managementBachelor's degree; some roles may require certification or training in data handling
Work EnvironmentTypically in clinical research teams, handling data systems and analysisAssists with data collection, entry, and quality checks in clinical trial sites or offices
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles involve working with clinical data, the Clinical Data Manager Ii focuses on data analysis, validation, and management within research teams, often requiring more technical skills. The Clinical Data Coordinator primarily handles data entry and quality control at the trial site level. Understanding these differences helps in choosing the right career path or job search focus.

What is a clinical data manager II?

A Clinical Data Manager II is responsible for overseeing the collection, validation, and management of clinical trial data to ensure its accuracy and integrity. They play a key role in designing data management plans, developing case report forms, and coordinating with clinical research teams to resolve data discrepancies. Additionally, they may supervise junior data managers, ensure compliance with regulatory standards, and prepare data for statistical analysis and regulatory submissions. This position typically requires several years of experience in clinical data management and a strong understanding of industry regulations such as GCP and FDA guidelines.

What opportunities for career advancement are available for a clinical data manager II?

As a Clinical Data Manager II, you can expect to progress to senior-level positions such as Senior Clinical Data Manager, Data Management Lead, or even Data Management Project Manager, depending on your experience and performance. Advancement often involves taking on more complex studies, overseeing larger teams, and contributing to strategic planning and process improvement. Networking within cross-functional teams and acquiring specialized certifications can further enhance your prospects. Organizations often support career growth through mentorship, training programs, and opportunities to lead projects.
What are popular job titles related to Clinical Data Manager Ii jobs in Raleigh, NC? For Clinical Data Manager Ii jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Data Manager Ii jobs in Raleigh, NC look for? The top searched job categories for Clinical Data Manager Ii jobs in Raleigh, NC are:
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Clinical Data Manager Ii jobs near you
Infographic showing various Clinical Data Manager Ii job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $115,582 per year, or $55.6 per hour.

Principal Clinical Data Manager

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Contractor

Re-posted 21 days ago

Job description

 Job Summary:
Manage end-to-end delivery of data management services concurrently for single/multi-service projects with little-to-no guidance, ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out, communications and milestone deliverables. Perform a leadership role in specific CDM tasks (e.g. Subject Matter Expert (SME)). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.
Responsibilities:
  • Effectively plan and execute multiple Data Management projects simultaneously. Provide updates directly to senior stakeholders as requested by line management.
  • Collaborate with Sponsor and stakeholders to develop effective project plans to include scope, goals, deliverables, required resources, risks, issues and milestone timing.
  • Assign tasks and responsibilities within Data Management to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business.
  • Ensure that assigned team executes Data Management functions in accordance with CRO and/or Sponsor Standard Operating Procedures (SOPs).
  • Provide guidance to less-experienced Data Management staff.
  • Assess ongoing and future project resource needs on an ongoing basis with feedback to Line Management.
  • Triage and resolve issues throughout project lifecycle.
  • Ensure that project team members' performance supports project budget and delivery requirements.
  • Effectively manage project scope by ensuring any changes to scope are documented and approved through appropriate change management processes.
  • Participate in and/or contribute to Sponsor and/or Regulatory audits/inspections.
  • Attend regular meetings with the sponsor and/or project team, for discussions relating to data management issues and provides status updates for the project.
  • Track and report quality and performance metrics and KPIs as needed.
  • Active participation in the organization and department of both in-house and external training courses.
  • Adherence to SOPs as well as current ICH-GCP guidelines and other applicable standards demanded by the Regulatory Authorities.
  • Coordinate and manage training for Investigators, Data Coordinators and CRAs on the selected Data Systems for Data Processing.
  • Ensure quality of data in accordance with DM control documents for accuracy, completeness, consistency and validity, generate and submit queries as necessary to investigation sites, as well as the project team at large.
  • Ensure all clinical data management tasks are complete prior to database lock.
  • Produce and/or coordinate reports and listings for team reviews and DSMBs (Data Safety Monitoring Boards).
  • Ensure the project team and the sponsor is kept informed of all issues and timelines together with quality and performance achieved.
  • Identify and recommend process improvements and standards to department management and implements approved process improvements.
  • Assists in development and review of SOPs.
  • Assist with special projects as designated by management.
  • Perform other duties as assigned by management.

Experience:
  • Proven knowledge of clinical data management process and clinical database systems
  • Excellent problem-solving, analytical, and communication skills.
  • Ability to work collaboratively in a fast-paced, team-oriented environment.
  • Strong leadership and mentorship skills.
  • Ability to work independently and manage multiple projects simultaneously.
  • Strong attention to detail and quality.
  • Extensive experience within the CRO industry
  • Extensive knowledge of Clinical Data Management System(s), including Electronic Data Capture system(s)

Education/Qualifications:
  • BS/RN in Life Sciences and/or combination of education and experience
  • Minimum of 8-10 years experience in clinical data management
  • Strong oral and written communication skills
  • Effective working knowledge of Microsoft Office Suite including Word, Excel, and Project
  • Demonstrated problem solving, analytical, organization, and time management skills
  • Demonstrated flexibility and ability to work well in a team environment
  • Demonstrated ability to be compliant with GCP/regional regulatory guidelines and SOPs

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