Data Management Associate Jobs
Data Management Associate jobs are open across healthcare, finance, government, and technology, covering specializations in data quality, database administration, and records management, from entry-level to senior associate roles. See the openings below and apply to the ones that match your experience.
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Job Description:
Company Overview
Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California.
Position Summary
The Associate Manager, Clinical Data Management will support data management activities for CRISPR studies across all stages of clinical drug development. Working closely with clinical study teams and cross functional stakeholders, they will help ensure that data capture systems, processes, and documentation produce accurate, consistent, complete, and high-quality clinical data. The role will include clinical data review, query management, and data reconciliation, with additional responsibilities spanning data management documentation, user acceptance testing, third-party vendor data, and GCP inspection readiness.
Responsibilities
- Plan, coordinate, and manage data management tasks and timelines.
- Collaborate with internal cross functional management to ensure all stakeholders’ needs are addressed.
- Lead the development of data management documentation including CRFs, CCGs, edit check specifications, SAE reconciliation plans, Coding plans, Data Management Plans, and third-party vendor data specifications; Coordinate related reviews with cross functional team(s).
- Ensure proper filing and documentation of clinical data management documents.
- Lead and participate in UAT of clinical data management systems.
- Lead and participate in clinical data review and data reconciliation.
- Prepare content and participate in study team meetings.
- Contribute to departmental SOP and process development/improvement and integration of technology.
- Support GCP inspection readiness.
Minimum Qualifications
- Bachelor’s Degree in a health-related field.
- 4-6+ years of clinical data management experience at Sponsor, CRO, and/or Investigative site.
- Knowledge and experience with Microsoft applications including Word, MS Project, PowerPoint.
- Knowledge and experience with major EDC databases including Medidata Rave, Veeva, etc.
- Experience developing reports using J-Review, BOXI, and/or other CDM reporting tools, including data visualization software.
- Knowledge and experience with CDASH/SDTM/CDISC standards.
- Experience working with central and specialty labs/vendors.
- Knowledge of medical terminology and medical coding dictionaries including MedDRA and WHODrug.
- Familiarity with GCP, ICH, and FDA requirements as applicable for Clinical Data Management.
- Able to manage multiple initiatives and shifting priorities within a small company environment.
- Strong analytical and problem-solving skills that meet or improve the status quo.
- Excellent interpersonal skills with the ability to work independently and collaboratively in a dynamic team environment.
- Excellent written and oral communication skills.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Preferred Qualifications
- Experience with global studies using an outsourced CRO model.
- Experience in early phase clinical drug development including first-in-human studies.
- Experience with drug development and management of data in rare genetic diseases, in vivo treatments, and/or CAR-T cell therapies.
Competencies
- Collaborative – Openness, One Team
- Undaunted – Fearless, Can-do attitude
- Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
- Entrepreneurial Spirit – Proactive. Ownership mindset.Responsibilities
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Associate Manager: Base pay range of $100,000 to $115,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics’ reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy
Job Description:
Company Overview
Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California.
Position Summary
The Associate Manager, Clinical Data Management will support data management activities for CRISPR studies across all stages of clinical drug development. Working closely with clinical study teams and cross functional stakeholders, they will help ensure that data capture systems, processes, and documentation produce accurate, consistent, complete, and high-quality clinical data. The role will include clinical data review, query management, and data reconciliation, with additional responsibilities spanning data management documentation, user acceptance testing, third-party vendor data, and GCP inspection readiness.
Responsibilities
- Plan, coordinate, and manage data management tasks and timelines.
- Collaborate with internal cross functional management to ensure all stakeholders’ needs are addressed.
- Lead the development of data management documentation including CRFs, CCGs, edit check specifications, SAE reconciliation plans, Coding plans, Data Management Plans, and third-party vendor data specifications; Coordinate related reviews with cross functional team(s).
- Ensure proper filing and documentation of clinical data management documents.
- Lead and participate in UAT of clinical data management systems.
- Lead and participate in clinical data review and data reconciliation.
- Prepare content and participate in study team meetings.
- Contribute to departmental SOP and process development/improvement and integration of technology.
- Support GCP inspection readiness.
Minimum Qualifications
- Bachelor’s Degree in a health-related field.
- 4-6+ years of clinical data management experience at Sponsor, CRO, and/or Investigative site.
- Knowledge and experience with Microsoft applications including Word, MS Project, PowerPoint.
- Knowledge and experience with major EDC databases including Medidata Rave, Veeva, etc.
- Experience developing reports using J-Review, BOXI, and/or other CDM reporting tools, including data visualization software.
- Knowledge and experience with CDASH/SDTM/CDISC standards.
- Experience working with central and specialty labs/vendors.
- Knowledge of medical terminology and medical coding dictionaries including MedDRA and WHODrug.
- Familiarity with GCP, ICH, and FDA requirements as applicable for Clinical Data Management.
- Able to manage multiple initiatives and shifting priorities within a small company environment.
- Strong analytical and problem-solving skills that meet or improve the status quo.
- Excellent interpersonal skills with the ability to work independently and collaboratively in a dynamic team environment.
- Excellent written and oral communication skills.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Preferred Qualifications
- Experience with global studies using an outsourced CRO model.
- Experience in early phase clinical drug development including first-in-human studies.
- Experience with drug development and management of data in rare genetic diseases, in vivo treatments, and/or CAR-T cell therapies.
Competencies
- Collaborative – Openness, One Team
- Undaunted – Fearless, Can-do attitude
- Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
- Entrepreneurial Spirit – Proactive. Ownership mindset.Responsibilities
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.
Associate Manager: Base pay range of $100,000 to $115,000+ bonus, equity and benefits
The range provided is CRISPR Therapeutics’ reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy
Data Management Associate Jobs by Experience Level
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Find JobsData Management Associate Job Market
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Science & Research
- Healthcare & Medical Services
- Consulting & Professional Services
What Employers Look For
The qualifications that appear most often in data management associate jobs.
- Proficiency in SQL for querying and maintaining relational databases
- Experience with data quality tools and data validation processes
- Familiarity with ETL pipelines and data integration workflows
- Bachelor's degree in information management, computer science, or a related field
- Knowledge of data governance frameworks and metadata management practices
- Experience with master data management platforms such as Informatica or SAP MDG
Tips for Your Data Management Associate Job Search
Tailor your resume to data tools
List every database platform, ETL tool, and data governance software you've used by name. Hiring managers for data management associate roles scan for SQL, Python, Tableau, or specific MDM platforms before reading anything else on your resume.
Highlight data quality wins with metrics
Quantify the impact of data cleanup or governance projects you've led or supported. Saying you reduced duplicate records by a measurable amount or improved ingestion accuracy is far more compelling than describing your responsibilities in general terms.
Target postings that name your certifications
Filter for openings that explicitly mention credentials you hold, such as CDMP or vendor-specific data certifications. Applying where your credentials are listed in the requirements puts you ahead of candidates who don't hold them.
Apply early to roles that fit
Migrate Mate lists data management associate openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Prepare a data stewardship scenario answer
Interviewers for data management associate roles frequently ask how you've handled conflicting data sources or enforced data standards across teams. Rehearse a specific example that walks through the problem, your process, and the outcome.
Negotiate by referencing data scope and volume
When discussing compensation, anchor your ask to the scale of data you manage, the systems you own, and any cross-functional responsibility. Candidates who frame their value around data complexity tend to negotiate more effectively than those who cite title alone.
Data Management Associate Jobs: Frequently Asked Questions
Which companies are hiring the most data management associates?
The most active employers for data management associates right now are Regeneron, JPMorganChase, and Capital One, and the most openings are in New Jersey, Massachusetts, and Virginia, based on current listings on Migrate Mate as of November 2026. Healthcare systems, financial institutions, and large government contractors tend to post the highest volumes of these roles consistently.
How many data management associate jobs are remote?
About 64% of data management associate openings are fully remote or hybrid as of November 2026, with the highest concentration of remote-eligible roles in data quality analysis and metadata management. Positions requiring hands-on database administration or close collaboration with infrastructure teams are more likely to require on-site work at least part of the week.
How do you become a data management associate?
Start by earning a bachelor's degree in information systems, computer science, or a closely related field. Build hands-on SQL skills through coursework or personal projects, then pursue a recognized data management certification such as the CDMP. Apply for entry-level data analyst or data coordinator roles to gain practical experience with governance processes, ETL workflows, and data quality tools before moving into an associate-level position.
Can you get a data management associate job with little or no experience?
Yes, some employers hire candidates with limited professional experience if you can demonstrate strong SQL fundamentals, familiarity with spreadsheet tools, and an understanding of basic data governance concepts. Building a portfolio of personal data projects, completing an online data management course, or earning an entry-level certification can substitute for work history when applying to associate roles at smaller organizations or in government agencies.
What does the data management associate interview process look like?
Most employers start with a recruiter screening call to confirm your background and tool familiarity, followed by a technical interview that may include a SQL exercise or a scenario involving data quality issues. A final round typically involves a panel with a data manager and a business stakeholder who assess how you communicate data problems to non-technical audiences. Some employers add a take-home data cleanup or mapping exercise before the final stage.
Where can I find and apply to data management associate jobs?
You can find and apply to data management associate jobs on Migrate Mate, which lists current openings from employers across the United States. Search for roles that match your experience level and specialization, then apply directly to each listing that fits.
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