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Manager Clinical Data Management Jobs (NOW HIRING)

Serves as project manager of all COA systems activities for protocols assigned.- Uses interpersonal ... Thorough knowledge of clinical data management * Effective written and verbal communication skills

Lead end-to-end clinical data management activities for companion diagnostic studies, including ... data acquisition, database design, data review, external data integration, reconciliation, quality ...

Actively participates in the development of processes, and documents, that support the clinical data management team. Huntsman Cancer Institute is committed to cancer prevention, care, and ...

Participate as the primary data management representative on Incyte multidisciplinary project teams and ensure effective communication exchange.* Responsible for communicating key clinical data ...

Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate, timely, and consistent clinical data. Build, review, and maintain clinical databases, data collection ...

Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of ... The CDM ensures, from a data management perspective, assigned trials on time, within budget, and ...

Clinical Data Managers

Campus, IL · On-site

$39K - $91K/yr

Data Management Plans * Edit specifications * SAE Reconciliation Guidelines * Other plans and ... The Clinical Data Manager II is expected to have a solid understanding of the regulatory framework ...

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Manager Clinical Data Management information

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

As of Sep 10, 2026, the average hourly pay for manager clinical data management in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are the roles and responsibilities of a manager clinical data management?

A Manager of Clinical Data Management oversees the collection, processing, and quality assurance of clinical trial data to ensure accuracy and regulatory compliance. They lead teams of data managers, develop data management plans, and coordinate with clinical and regulatory teams to resolve data discrepancies. Their responsibilities often include implementing data standards, ensuring data integrity, and supporting audits and submissions to regulatory authorities. This role requires strong leadership skills, attention to detail, and expertise in clinical trial processes and data management systems.

What are the key skills and qualifications needed to thrive as a manager clinical data management?

To thrive as a Manager Clinical Data Management, you typically need a strong background in life sciences, clinical research, and data management, often supported by a relevant degree and experience in clinical trials. Expertise with clinical data management systems (such as Medidata Rave or Oracle Clinical), knowledge of CDISC standards, and certifications like CCDM are highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring data integrity. These skills are essential to ensure high-quality, compliant clinical data that supports successful regulatory submissions and advances clinical research.

What are some typical challenges faced by a manager clinical data management, and how can they be addressed?

Managers in Clinical Data Management often face challenges such as ensuring data quality across multiple clinical sites, meeting tight regulatory deadlines, and coordinating cross-functional teams including data analysts, clinical operations, and biostatisticians. To address these challenges, strong project management skills, proactive communication, and the implementation of robust data validation procedures are essential. Additionally, staying up-to-date with evolving regulatory requirements and investing in team training can help maintain data integrity and streamline workflows.

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

AspectManager Clinical Data ManagementClinical Data Coordinator
ResponsibilitiesOversees data management processes, manages teams, ensures data quality and complianceCollects, enters, and verifies clinical trial data, supports data cleaning
Required SkillsProject management, leadership, data management expertiseAttention to detail, data entry, basic understanding of clinical data
CertificationsCDMP, SAS, or related certifications often preferredTypically no advanced certifications required
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsSimilar settings, often working under supervision of managers

While both roles involve clinical data, the Manager Clinical Data Management leads data strategies and teams, whereas the Clinical Data Coordinator focuses on data entry and verification tasks. The manager role requires more leadership and strategic skills, while the coordinator role is more operational and detail-oriented.

What cities are hiring for Manager Clinical Data Management jobs?

Cities with the most Manager Clinical Data Management job openings:

What are the most commonly searched types of Clinical Data Management jobs?

The most popular types of Clinical Data Management jobs are:

What states have the most Manager Clinical Data Management jobs?

States with the most job openings for Manager Clinical Data Management jobs include:

What are popular job titles related to Manager Clinical Data Management jobs?

For Manager Clinical Data Management jobs, the most frequently searched job titles are:

Infographic showing various Manager Clinical Data Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.

Sr. Director, Clinical Data Management

South San Francisco, CA • On-site

ALX Oncology Inc.
Biotechnology Research and Development • 11 - 50 employees

Full-time

Retirement

Re-posted 24 days ago


Job description

Reporting to the VP, Biometrics, the Sr. Director, Clinical Data Management provides strategic and operational leadership for the Clinical Data Management function across ALX Oncology's development portfolio. As the senior data management leader in a lean biotechnology environment, this individual is responsible for establishing a scalable, fit-for-purpose function that delivers high-quality clinical trial data to support development milestones, regulatory submissions, and future portfolio growth. This role requires a leader who can think strategically while remaining hands-on, building effective partnerships and driving operational excellence in a dynamic, resource-focused organization.

Preference will be given to candidates who can regularly work onsite Mondays and Tuesdays as part of the company's hybrid work model.

Key Responsibilities include:

  • Lead the Clinical Data Management function by developing and executing strategies, processes, and operational plans that support ALX Oncology's clinical development portfolio and align with the objectives of the Biometrics organization.
  • Oversee Clinical Data Management activities across the development portfolio, including review and approval of key deliverables such as database design, eCRFs, edit checks, data review plans, and database lock activities.
  • Lead data review, issue management, and milestone readiness to support interim analyses, database locks, and key development milestones.
  • Serve as the primary escalation point for data management issues affecting study quality, timelines, or regulatory readiness.
  • Oversee EDC and related clinical data systems, including implementation, configuration, and vendor management.
  • Lead the selection, oversight, and performance management of CROs and specialty vendors, establishing governance, performance metrics, and communication processes to ensure high-quality execution and accountability.
  • Manage vendor budgets and identify cost-effective solutions without compromising quality or compliance.
  • Drive continuous improvement initiatives that enhance data quality, operational efficiency, and study execution.
  • Partner with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical, Safety, Regulatory, and Quality to support successful study execution.
  • Provide data management expertise during protocol development, advising on data collection strategy, endpoint feasibility, and study design.
  • Ensure clinical data are inspection-ready and support regulatory submissions, audits, safety reviews, and due diligence activities.
  • Contribute to a culture that reflects ALX's values by acting with integrity, accountability, transparency, and respect. Build strong, collaborative relationships through active engagement with colleagues, including regular onsite participation consistent with the company's hybrid work model.

Not sure if you are qualified for this position?  We know that skills and experience can show up in different ways and we welcome resumes from a broad range of applicants.  You are encouraged to apply even if you do not meet each of the preferred qualifications.

Preferred Qualifications include:

  • Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related scientific discipline, or an equivalent combination of education and directly relevant work experience. Advanced degree (MS, MPH, PhD) is a plus.
  • Approximately 12+ years of progressive Clinical Data Management experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III clinical studies, with demonstrated success leading outsourced Clinical Data Management activities, partnering across functions, and delivering high-quality clinical trial data. Experience supporting regulatory submissions is preferred. Oncology and/or immuno-oncology experience is strongly preferred.
  • Strong knowledge of Clinical Data Management principles, GCP, applicable regulatory requirements, CDISC standards, and industry best practices, with demonstrated expertise in database design, data cleaning, medical coding, external data reconciliation, data review, database lock, and other core Clinical Data Management processes. Experience with leading EDC platforms such as Medidata Rave, Veeva EDC, Oracle Clinical, or equivalent systems.
  • Demonstrated ability to effectively manage CROs, vendors, budgets, and outsourced Clinical Data Management activities.
  • Strategic, collaborative leader with excellent communication, organizational, and relationship-building skills, capable of influencing cross-functional teams and external partners.
  • Demonstrated ability to prioritize competing demands, solve complex problems, build scalable processes, and adapt to evolving business priorities while contributing beyond functional boundaries in a fast-paced, resource-constrained environment.

 

Compensation

The salary range for this position at our South San Francisco, CA corporate office is $240,000 - $280,000. Additional factors such as academic credentials and relevant experience will influence the actual salary offered. In addition to a competitive market-based salary, ALX Oncology offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package including 401K.  Additional information can be found here:  https://alxoncology.com/careers/

 

About ALX Oncology

ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.

Information for Recruitment Agencies

Please note that ALX Oncology does not accept unsolicited resumes or candidate information from recruitment agencies, including blinded or anonymized resumes, and will not be responsible for any fees associated with unsolicited submissions.  Do not contact hiring managers or other ALX Oncology employees directly. Recruiting activities are managed through our Human Resources team.