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Remote Clinical Data Manager Contract Jobs in Raleigh, NC

AKIVA AI

Program Manager / Contract Manager

Raleigh, NC · Remote

$125K - $185K/yr

North Carolina (Remote with periodic on-site coordination at participating community colleges ... Position Overview AKIVA is seeking a Program Manager / Contract Manager to serve as the primary ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

... manage clinical, operational, and data-related responsibilities while ensuring compliance with ... This position is not eligible for visa sponsorship #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a ...

Cloudera

Contracts Manager

Raleigh, NC · Remote

$86K - $115K/yr

Compile and analyze contract-related data while maintaining accurate historical contract ... Employee Resource Groups EEO/VEVRAA #LI-Remote #li-KB1

VocoVision

Virtual SLP in NC

Raleigh, NC · Remote

This contract role supports students by delivering speech therapy through an advanced virtual platform designed to facilitate effective remote clinical sessions. Key Responsibilities: * Conduct ...

Biodata Partners, Inc.

Senior Medical Coder

Raleigh, NC · On-site +1

$16 - $21.50/hr

Manage end-to-end delivery of clinical data management coding responsibilities concurrently for single/multiple projects ensuring quality and timeliness. Provide leadership and mentorship to Medical ...

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Remote Clinical Data Manager Contract information

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How much do remote clinical data manager contract jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for remote clinical data manager contract 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 are some common challenges faced by Remote Clinical Data Managers working on a contract basis, and how can they be managed?

Remote Clinical Data Managers on contract often encounter challenges such as coordinating efficiently with cross-functional teams in different locations and time zones, maintaining data integrity across multiple platforms, and adapting quickly to new study protocols or sponsor requirements. Effective communication tools, regular virtual meetings, and well-organized documentation can help bridge gaps and ensure smooth collaboration. Staying proactive in seeking clarifications and leveraging project management software are also key strategies for managing remote workflow and meeting tight study timelines.

What is a Remote Clinical Data Manager Contract?

A Remote Clinical Data Manager Contract is a temporary, project-based position where a professional oversees the collection, validation, and management of clinical trial data from a remote location. Clinical Data Managers ensure the accuracy, integrity, and compliance of data used in clinical research, collaborating with study teams and using specialized software. Working remotely allows for flexibility and may involve coordinating across different time zones, but the core responsibilities remain the same as onsite roles. Contract positions typically last for the duration of a specific trial or project.

What are the key skills and qualifications needed to thrive as a Remote Clinical Data Manager on a contract basis, and why are they important?

To thrive as a Remote Clinical Data Manager on contract, you need expertise in clinical data management, database design, and a background in life sciences or related fields, often supported by a relevant degree. Familiarity with data management systems like Medidata Rave, Oracle Clinical, and knowledge of CDISC standards or certifications such as CCDM are highly valued. Strong attention to detail, excellent organizational skills, and effective remote communication are crucial soft skills for success in this role. These competencies ensure the accuracy, integrity, and security of clinical trial data, which is vital for regulatory compliance and successful study outcomes.

What is the difference between Remote Clinical Data Manager Contract vs Remote Clinical Data Coordinator?

AspectRemote Clinical Data Manager ContractRemote Clinical Data Coordinator
CredentialsBachelor's in Life Sciences, Biostatistics, or related field; experience with data management systemsSimilar credentials; often entry to mid-level experience in data entry and management
Work EnvironmentContract-based, remote, project-specificRemote, often full-time or part-time, supporting clinical trial data collection
Employer & Industry UsagePharmaceuticals, biotech, CROsPharmaceuticals, clinical research organizations, healthcare companies

The Remote Clinical Data Manager Contract focuses on managing and analyzing clinical trial data on a contractual basis, requiring advanced data management skills. The Remote Clinical Data Coordinator handles data entry and coordination tasks, often supporting data collection processes. Both roles are remote and industry-specific, but differ in scope and level of responsibility.

What are the most commonly searched types of Remote Clinical Data Manager jobs in Raleigh, NC? The most popular types of Remote Clinical Data Manager jobs in Raleigh, NC are:
What are popular job titles related to Remote Clinical Data Manager Contract jobs in Raleigh, NC? For Remote Clinical Data Manager Contract jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Data Manager Contract jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Data Manager Contract jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Data Manager Contract jobs? Cities near Raleigh, NC with the most Remote Clinical Data Manager Contract job openings:
Remote Clinical Data Manager Contract jobs near you

Principal Clinical Data Manager

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Contractor

Posted 22 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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