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Manager Clinical Data Management Jobs (NOW HIRING)

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in ...

asrcfh

Clinical Data Manager 3

San Antonio, TX · On-site

Ensure consistency, accuracy, and adherence to federal regulations, Good Clinical Practice, Good Clinical Data Management Practices, as well as SOPs and Working Instructions * Manage patient protocol ...

Eisai

Senior Manager, Clinical Data Science

The Data Science Group is seeking a Senior Manager, Clinical Data Science to drive drug development through contributions to predictive modeling of disease characteristics and drug response. The role ...

Abbott

MN · On-site

$45 - $47/hr

Education and work experience in project management, life sciences and/or technical field. Knowledge of data collection best practices for clinical trials. Knowledge of global clinical operations.

Triwill Group

This role offers the opportunity to lead clinical data management activities across the full lifecycle of complex clinical studies. You will serve as a senior data management expert and primary ...

ImmunityBio

Senior Clinical Data Manager

Dunkirk, NY · On-site

Position Summary The Senior Clinical Data Manager is an expert in clinical data management with ... Data Management Plan * CRF Completion Guidelines * Coding Guidelines * Annotated CRFs * Edit Check ...

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

As of Sep 11, 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.

Clinical Data Manager

Redmond, WA • On-site

SystImmune, Inc
Biotechnology Research and Development • 1 - 10 employees
Learn more about SystImmune, Incexternal

$100K - $170K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago

Job description

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has several assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables. The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in overseeing CROs and vendors to meet study needs and deliverables.
This position requires you to be onsite full-time in Redmond, WA.Responsibilities:
  • Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out.
  • Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. Utilize templates and standard guidelines to initiate documents, but demonstrate critical thinking, alignment-building and discretion to tailor documents to study needs.
  • Independently lead data cleaning activities such as, but not limited to, study team data reviews, Non-system Edit Check Output review, SAE reconciliation, and non-CRF data reconciliation. Gather cross-functional input to drive creation of custom data review plans. Evaluate options and exercise discretion to choose efficient and effective issues resolution paths.
  • Manage data deliverables processes and database locks, with high quality and efficiency.
  • Foster collaboration and relationship-building with all study team representatives (e.g. Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical Writers, Regulatory representatives, etc.)
  • DM Project Management: With oversight, ensure data management deliverables are met on time. Utilize communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities. Ensure study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. Provide solutions for data management issues that arise during study conduct.
  • Manage/coordinate work performed by vendors/CROs as appropriate to ensure quality of product. Assist in the selection of vendors/CROs (e.g. review RFPs, attend site audits)
  • Performs Medical Coding as needed, works with CROs, Medical Monitors, and Clinical Scientists to coordinate activities for the medical review of clinical trial data.
  • Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output. Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as appropriate for skill level.
  • Evaluate CDM processes and applications for improvements; participate in working groups to develop and implement new processes and applications.
  • Participate in development of DM specific SOPs.
  • Responsible for oversight of CRO data management activities and integrating the various functional group input.
  • All other duties as assigned.
Qualifications:
  • BA or BS and a minimum of 4 years of relevant experience.
  • Technologically savvy; quickly picks-up new information, standards, regulations, tools, methods or software as it relates to position and profession.
  • Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC).
  • SAS programming experience.
  • Experience with managing Lab Data, such as PK, PD, and Biomarkers.
  • Detail-oriented; performs quality and accurate work.
  • Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and GCDMP.
  • Strong knowledge of clinical research, drug development process, and medical terminology, oncology experience preferred.
  • Knowledge and understanding of DM Lifecycle associated with P1-P3 studies, including pivotal, blinded, and randomized trials.
  • Knowledge of MedDRA and WHO Drug coding.
  • Project Management skills, ability to manage multiple projects and meet deadlines.
  • Strong interpersonal, organizational, and communication skills.
  • Prior experience writing specification documents and/or work instructions.
  • Previous vendor/CRO management.
  • Previous experience with RTSM, eCOA/ePRO systems.

Compensation and Benefits:
The expected base salary range for this position is $100,000 - $170,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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