Clinical Data Manager Jobs
Clinical Data Manager jobs are open across pharmaceutical, biotech, medical device, and contract research organizations, from entry-level data coordinator to senior and principal levels, with specializations in oncology trials, EDC system management, and regulatory submissions. Find a role that fits below and apply directly.
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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
Clinical Data Manager Jobs by Experience Level
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Find Clinical Data Manager JobsClinical Data Manager Job Market
Who's Hiring
- Katalyst Healthcares & Life Sciences41
- AbbVie8
- Veeva Systems7
- Cedars-Sinai Medical Center7
- MRO Corporation6
Top Industries Hiring
- Biotechnology & Pharmaceuticals19
- Education9
- Healthcare & Medical Services7
- Consulting & Professional Services5
- Technology & Software3
What Employers Look For
The qualifications that appear most often in clinical data manager jobs.
- Bachelor's degree in life sciences, health informatics, or a related field
- Hands-on experience with EDC platforms such as Medidata Rave or Veeva Vault
- Proficiency in developing and maintaining data management plans for clinical trials
- Knowledge of CDISC standards including CDASH and SDTM data models
- Experience with database lock procedures, discrepancy management, and SAE reconciliation
- SCDM Good Clinical Data Management Practice certification preferred for senior roles
Tips for Your Clinical Data Manager Job Search
Tailor your resume to EDC systems
Hiring managers scan for named platforms like Medidata Rave, Oracle Clinical, or Veeva Vault. List every EDC and CTMS you have hands-on experience with, including version or module if relevant. Burying those names deep in a job description kills your chances.
Apply early to roles that fit
Migrate Mate lists clinical data manager openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Filter by therapeutic area to target openings
Oncology, rare disease, and neurology trials each use distinct data collection standards and oversight requirements. Searching by therapeutic area rather than job title alone surfaces postings that match your actual protocol experience, making your application far more competitive.
Quantify your data validation outcomes
Replace vague bullets like 'managed database lock' with specifics: number of studies, timelines hit, or discrepancy resolution rates you achieved. Reviewers weigh concrete data quality metrics heavily when comparing candidates at the same seniority level.
Prepare a protocol walk-through for interviews
Clinical data manager interviews frequently include a scenario where you walk through how you would set up a data management plan for a given protocol. Practice articulating your edit check logic, SAE reconciliation approach, and database lock process out loud before the call.
Negotiate scope before accepting a title
Two job offers with identical titles can differ dramatically in study portfolio size, sponsor complexity, and cross-functional authority. Ask directly how many studies you own at once and whether the role owns DMP authorship, so you compare the actual jobs, not just the titles.
Clinical Data Manager Jobs: Frequently Asked Questions
Which companies are hiring the most clinical data managers?
Katalyst Healthcares & Life Sciences, AbbVie, and Veeva Systems are hiring the most clinical data managers right now, with openings concentrated in California, New Jersey, and Massachusetts, based on current listings on Migrate Mate as of November 2026. Contract research organizations and large pharmaceutical sponsors consistently post the highest volume of openings across seniority levels.
How many clinical data manager jobs are remote?
About 75% of clinical data manager openings are fully remote or hybrid as of November 2026, making it one of the more remote-accessible roles in clinical operations. Positions focused on EDC system oversight, data review, and DMP authorship are the most likely to be offered with full location flexibility, while on-site study startup roles are less commonly remote.
How do you become a clinical data manager?
Start with a degree in life sciences, health informatics, nursing, or a related field, then gain hands-on experience as a clinical data coordinator or data entry associate on sponsored trials. Build proficiency in at least one major EDC platform, learn CDISC data standards, and pursue SCDM certification once you have direct data management experience. Moving into a manager role typically requires demonstrated ownership of a full study data management plan from protocol setup through database lock.
Can you get a clinical data manager job with little experience?
Yes, but you need to position your entry strategically. Employers hiring junior clinical data managers prioritize hands-on exposure to clinical trial data, even from a coordinator or data entry role, over years of experience. Completing a CDISC fundamentals course, getting certified in a widely used EDC platform, and applying to CROs that run large trial portfolios and promote from within gives you the most realistic path into a first manager-level role.
What does the clinical data manager interview process look like?
Most interview processes include an initial recruiter screen focused on EDC experience and study type background, followed by a technical interview with a data management lead or director covering your DMP development process, edit check logic, and database lock procedures. A final round often involves a panel with cross-functional stakeholders from biostatistics or clinical operations and may include a scenario-based exercise where you walk through how you would set up data management for a described protocol.
Where can I find and apply to clinical data manager jobs?
You can find and apply to clinical data manager jobs on Migrate Mate, which lists current openings from across the United States in one place. Find roles that match your experience level and therapeutic area focus, then apply directly to each listing that fits.
See All 281+ Clinical Data Manager Jobs
Find roles that match your experience and apply in just a few clicks.
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