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Title Manager Jobs in Raleigh, NC (NOW HIRING)

ORGANIZATIONAL REPORTING Supervisor Title * Manager outbound Position Reporting to this Role * Forklifts * Clerical * Selectors BENEFITS INFORMATION: For information on Sysco's Benefits, please visit ...

Job Title Manage and lead the Service Desk and Global Account Management (GAM) teams, ensuring alignment with industry best practices. Drive onboarding of new mergers and acquisitions (M&A) into ...

Manages and coordinates Title I program activities and assigned staff for the implementation of Title I programs as an integral part of the total curriculum and instructional program, in accordance ...

Manages and coordinates Title I program activities and assigned staff for the implementation of Title I programs as an integral part of the total curriculum and instructional program, in accordance ...

ORGANIZATIONAL REPORTING Supervisor Title * Manager outbound Position Reporting to this Role * Forklifts * Clerical * Selectors BENEFITS INFORMATION: For information on Sysco's Benefits, please visit ...

Showing results 21-40

Title Manager information

See Raleigh, NC salary details

$10.7K

$66.6K

$95.7K

How much do title manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for title manager in Raleigh, NC is $66,608.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,400.00 and $73,900.00 per year, depending on experience, location, and employer.

What does a title manager do?

A Title Manager oversees the title process in real estate or automotive transactions, ensuring proper documentation, compliance with regulations, and resolving title issues. They coordinate with lenders, buyers, and sellers to verify ownership history and clear any encumbrances. Their responsibilities also include managing a team of title officers, reviewing legal documents, and ensuring timely closings. Strong attention to detail and knowledge of relevant laws are essential for success in this role.

What are the key skills and qualifications needed to thrive as a title manager?

To thrive as a Title Manager, you need expertise in title searches, real estate transactions, and document management, often supported by a related degree or significant industry experience. Familiarity with title and escrow software, land records databases, and state regulatory systems is typically required, and certification as an escrow officer or title professional can be advantageous. Strong attention to detail, organizational skills, and effective communication are key soft skills for success in this position. These skills ensure the accurate processing of property titles, compliance with legal standards, and smooth coordination among clients, lenders, and colleagues.

What are the most commonly searched types of Title jobs in Raleigh, NC? The most popular types of Title jobs in Raleigh, NC are:
What are popular job titles related to Title Manager jobs in Raleigh, NC? For Title Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Title Manager jobs in Raleigh, NC look for? The top searched job categories for Title Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Title Manager jobs? Cities near Raleigh, NC with the most Title Manager job openings:
Infographic showing various Title Manager 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 $66,608 per year, or $32 per hour.

Senior/Principal Clinical Programmer

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Full-time

Re-posted 19 days ago


Job description

Job Title: Principal Clinical Programmer
Job Code: CDM0016
Department Name: Clinical Data Management
Reports to Title: Manager or above
Job Summary:
The Principal Clinical Programmer is a member of the Data Management team and serves as a subject matter expert for Clinical Data Programming, Reporting, Process, and technology. Accountable for the quality and delivery of the Data Management programming, reporting and visualization, standard, and exception data listings across studies. Scope of work includes oversight and expertise in the design, development, and validation of programs, standard and adhoc reports, standard and exception data listings, and visualizations to support ongoing data review activities, achieve critical study milestones, and gain data insights into our clinical studies. The position requires good understanding of programming methods and techniques, critical thinking, and complex problem-solving skills. This position will require strong collaboration in working with other members of the Biostatistics and Data Management, external CRO partners, and other stakeholders.
Responsibilities:
  • Serve as a subject matter expert and provide expertise for Database programming, Reporting, and Technology and optimize the use of J-Review, ETL, SAS tools, and others to support business needs.
  • Manage the quality of the data management clinical database programming deliverables including edit checks programming, complex reports, and listings; patient profiles, subject narratives, exception listings, dose modification reports, and other adhoc reports using JReview & SAS as part of standard data validation and reporting package for clinical studies.
  • Develop and/or provide oversight on the programming specifications for the data validation and reporting deliverables; code, test, and document deliverables conforming to programming standards, data quality and governance, and validation policies.
  • Partner with internal and external stakeholders to ensure timely delivery of data management programming, EDC database, external data, data management programming of reports and listings including the use of visualization tools.
  • Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
  • Develop standard programs, templates, reports, data listings, discrepancy reports, and patient profiles to facilitate in the ongoing review of clinical data during study conduct and study closeout.
  • Build, test, and scale-up programs for data validation derivation procedures, data reports, listings, and SAS on Demand relational database extracts for operational use, identification of data outliers, quality inconsistencies, and preparation for analysis.
  • Provide technical guidance and direct programming tasks for Medical Coding activities.
  • Provide Clinical Programming expertise and support for critical and time-sensitive study milestones including interim analysis, and database lock activities.
  • Perform ETL tasks, enhancements, validation, and maintenance of the programs and templates on an ongoing basis.
  • Perform QC, lead unit testing activities, develop validation scripts for user acceptance, manage and execute programs and dry runs as needed, and resolve programming issues proactively.
  • Develop and maintain mapping, and program specifications for standard reports, listings, and visualizations.
  • Maintain database programming checklists and trackers to ensure conformance of high-quality deliverables with the study data validation and reporting package.
  • Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.
  • Participate in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

Experience:
  • Minimum of 5 years database programming experience and data validation programming in the device/pharmaceutical/CRO industry.
  • Expertise in Clinical Programming, methods, and techniques
  • Expertise in using standard reporting and data visualization tools including JReview, and SAS tools.
  • Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm)
  • Knowledge of CDISC data standards.
  • Knowledge and understanding of relational databases.
  • Clinical Programming, Project Management, and Technical Expertise
  • Knowledge of logical data design and data mapping
  • Knowledge of reporting and data visualization tools: JReview, Spotfire, SAS suite and ETL technology
  • Experience with programming development, validation, execution, maintenance, documentation, and archival of clinical data for regulatory submission is required.
  • Proficient in industry standards, medical terminology, and clinical trial methodologies.

Education:
  • Bachelor of Science degree in Computer Science, Mathematics, or related area with relevant experience
  • Other degrees and certifications considered if commensurate with related data management experience