Clinical Data Management Jobs
Clinical data management jobs are open across pharmaceutical, biotech, CRO, and medical device industries, from entry-level data coordinators to senior managers and directors, with specializations in EDC systems, clinical trial databases, and data quality oversight. Find a role that fits from the openings below and apply directly.
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INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. 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 multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking an experienced and strategic Director, Clinical Data Management to lead the clinical data management function across our portfolio. This individual will be responsible for overseeing all aspects of clinical data management activities from study start-up through database lock and regulatory submission. The Director will provide leadership for internal and external data management teams, ensure high-quality and inspection-ready clinical data, and contribute to the development and execution of data management strategies supporting global clinical trials.
The successful candidate will collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Pharmacovigilance, Regulatory Affairs, and external partners to ensure timely and compliant delivery of clinical data for decision-making and regulatory submissions.
This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations.
Responsibilities:
- Lead and oversee the Clinical Data Management function, including strategy, standards, processes, and operational execution across the development portfolio.
- Build and scale a high-performing data management infrastructure to support a growing clinical pipeline.
- Serve as a key cross-functional leader in clinical development planning and execution.
- Oversee all data management activities for Phase I–III clinical trials from study start-up through database lock and regulatory submission.
- Ensure the delivery of high-quality, complete, and reliable clinical data through effective data review, issue management, and quality oversight.
- Drive timely database lock and submission-ready data deliverables in accordance with study timelines.
- Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory requirements, while maintaining inspection readiness.
- Establish and maintain CDISC-compliant data standards and industry best practices to support regulatory submissions.
- Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, and Safety teams to support study execution, data review, and submission readiness.
BASIC QUALIFICATIONS
- Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field required; Master's degree preferred.
- Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
- At least 5 years of leadership experience managing data management teams, vendors, and CRO partnerships.
- Significant experience supporting oncology clinical trials across early- and late-stage development.
- Demonstrated experience supporting regulatory submissions (NDA, BLA, MAA) and health authority inspections.
- Expertise with EDC systems, external data integrations, data reconciliation, and database management.
- Strong knowledge of clinical trial databases, CDISC standards, coding dictionaries (e.g., MedDRA, WHO Drug), and clinical data workflows.
- Familiarity with risk-based quality management principles, GCP requirements, and clinical development processes.
- Working knowledge of biostatistics, statistical analysis, and clinical data reporting to support cross-functional collaboration.
- Proven leadership, strategic thinking, problem-solving, communication, and stakeholder management skills, with a track record of driving cross-functional collaboration and operational excellence in a fast-paced biotech environment.
PREFERRED QUALIFICATIONS
- Oncology and/or antibody-drug conjugate (ADC) development experience.
- Experience managing global clinical trials across multiple regions.
- Prior experience in a growing biotechnology company.
COMPENSATION AND BENEFITS:
The expected base salary range for this position is $190,000 - $250,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level 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.
INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. 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 multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking an experienced and strategic Director, Clinical Data Management to lead the clinical data management function across our portfolio. This individual will be responsible for overseeing all aspects of clinical data management activities from study start-up through database lock and regulatory submission. The Director will provide leadership for internal and external data management teams, ensure high-quality and inspection-ready clinical data, and contribute to the development and execution of data management strategies supporting global clinical trials.
The successful candidate will collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Pharmacovigilance, Regulatory Affairs, and external partners to ensure timely and compliant delivery of clinical data for decision-making and regulatory submissions.
This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations.
Responsibilities:
- Lead and oversee the Clinical Data Management function, including strategy, standards, processes, and operational execution across the development portfolio.
- Build and scale a high-performing data management infrastructure to support a growing clinical pipeline.
- Serve as a key cross-functional leader in clinical development planning and execution.
- Oversee all data management activities for Phase I–III clinical trials from study start-up through database lock and regulatory submission.
- Ensure the delivery of high-quality, complete, and reliable clinical data through effective data review, issue management, and quality oversight.
- Drive timely database lock and submission-ready data deliverables in accordance with study timelines.
- Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory requirements, while maintaining inspection readiness.
- Establish and maintain CDISC-compliant data standards and industry best practices to support regulatory submissions.
- Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, and Safety teams to support study execution, data review, and submission readiness.
BASIC QUALIFICATIONS
- Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field required; Master's degree preferred.
- Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
- At least 5 years of leadership experience managing data management teams, vendors, and CRO partnerships.
- Significant experience supporting oncology clinical trials across early- and late-stage development.
- Demonstrated experience supporting regulatory submissions (NDA, BLA, MAA) and health authority inspections.
- Expertise with EDC systems, external data integrations, data reconciliation, and database management.
- Strong knowledge of clinical trial databases, CDISC standards, coding dictionaries (e.g., MedDRA, WHO Drug), and clinical data workflows.
- Familiarity with risk-based quality management principles, GCP requirements, and clinical development processes.
- Working knowledge of biostatistics, statistical analysis, and clinical data reporting to support cross-functional collaboration.
- Proven leadership, strategic thinking, problem-solving, communication, and stakeholder management skills, with a track record of driving cross-functional collaboration and operational excellence in a fast-paced biotech environment.
PREFERRED QUALIFICATIONS
- Oncology and/or antibody-drug conjugate (ADC) development experience.
- Experience managing global clinical trials across multiple regions.
- Prior experience in a growing biotechnology company.
COMPENSATION AND BENEFITS:
The expected base salary range for this position is $190,000 - $250,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level 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.
See All 75+ Clinical Data Management Jobs
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Find Clinical Data Management JobsClinical Data Management Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Katalyst Healthcares & Life Sciences4
- Revolution Medicines4
- Celgene Corporation3
- Eikon Therapeutics3
- Exelixis3
Top Industries Hiring
- Biotechnology & Pharmaceuticals35
- Consulting & Professional Services10
- Healthcare & Medical Services10
- Technology & Software10
- Education5
What Employers Look For
The qualifications that appear most often in clinical data management jobs.
- Bachelor's degree in life sciences, health informatics, or a related field
- Hands-on experience with EDC systems such as Medidata Rave or Oracle Inform
- Working knowledge of CDISC standards including CDASH and SDTM
- Familiarity with ICH E6 Good Clinical Practice guidelines and regulatory requirements
- Experience authoring or reviewing Data Management Plans and data validation specifications
- SCDM or CCDM certification is a preferred or required qualification at many sponsors and CROs
Tips for Your Clinical Data Management Job Search
Tailor your resume to EDC platforms
Hiring managers scan for specific system experience first. Call out every EDC tool you've used, Medidata Rave, Oracle Inform, Veeva Vault, and your role in each study, whether you built forms, validated data, or managed listings.
Highlight CDISC standards knowledge prominently
CDASH and SDTM compliance appear in almost every job posting. If you've mapped raw data to submission-ready SDTM domains or supported FDA submissions, put that on page one of your resume, not buried in a bullet.
Target roles by phase and therapeutic area
Phase I oncology trials have very different data complexity than Phase III cardiovascular studies. Filter openings by therapeutic area or phase if the listings allow it, and match your cover letter language to the specific program the employer is running.
Apply early to roles that fit
Migrate Mate lists clinical data management openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Prepare for a data review technical screen
Many CDM interviews include a live or take-home discrepancy review exercise. Practice identifying missing values, out-of-range flags, and protocol deviations in a sample listing so you can walk through your decision-making process clearly.
Negotiate scope, not just compensation
After an offer, ask whether the role covers one study or a portfolio, how many external vendors you'll manage, and whether DMP authorship is expected. These factors affect workload and career growth more than title alone.
Clinical Data Management Jobs: Frequently Asked Questions
Which companies are hiring the most clinical data managements?
The companies hiring the most clinical data managements right now include Katalyst Healthcares & Life Sciences, Revolution Medicines, and Celgene Corporation, with the largest share of openings in New Jersey, Massachusetts, and California, based on current listings on Migrate Mate as of June 2026. Large CROs and mid-size biotech sponsors tend to post the highest volume of openings consistently throughout the year.
How many clinical data management jobs are remote?
About 29% of clinical data management openings are fully remote or hybrid as of June 2026, making it one of the more remote-accessible roles in clinical operations. Database build, data review, and DMP authorship tasks transfer well to remote settings, while site-facing or vendor oversight roles more often require at least partial on-site presence.
How do you become a clinical data management?
Start with a bachelor's degree in a life science, health informatics, or statistics field, then gain exposure to clinical trial processes through an entry-level role such as clinical data coordinator or data entry associate. Build proficiency in at least one major EDC platform, study CDISC standards through free CDISC online training modules, and pursue SCDM membership or the CCDM credential once you have hands-on study experience to document.
Can you get a clinical data management job with little experience?
Yes, entry-level clinical data coordinator and junior CDM roles at CROs are specifically designed for candidates with limited direct experience. Employers at this level prioritize attention to detail, familiarity with spreadsheet tools, and basic understanding of GCP over years on the job. A relevant internship, academic research project involving data collection, or completion of an EDC training course can offset a thin work history during early applications.
What does the clinical data management interview process look like?
Most CDM interviews begin with a phone or video screen focused on your study experience and EDC background, followed by a technical round where you may be asked to walk through a data discrepancy scenario or explain how you'd build a validation check. Senior roles often add a panel interview with biostatistics or clinical operations stakeholders and may include a take-home data review exercise before a final offer conversation.
Where can I find and apply to clinical data management jobs?
You can find and apply to clinical data management jobs on Migrate Mate, which lists current openings from across the United States in one place. Find roles that match your experience level, therapeutic area, or preferred work arrangement and apply directly to each listing without leaving the platform.
See All 75+ Clinical Data Management Jobs
Jump back to the full list of openings and apply to any clinical data management role that fits.
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