Clinical Data Associate Jobs
Clinical Data Associate jobs are open across pharmaceutical, biotech, medical device, and CRO sectors, from entry-level to senior and lead roles, with specializations in EDC management, clinical trial data review, and regulatory compliance. 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 Associate Jobs by Experience Level
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Find Clinical Data Associate JobsClinical Data Associate Job Market
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Healthcare & Medical Services
- Science & Research
What Employers Look For
The qualifications that appear most often in clinical data associate jobs.
- Bachelor's degree in life sciences, health informatics, or a related field
- Hands-on experience with EDC platforms such as Medidata Rave or Oracle Clinical
- Proficiency in data cleaning, query management, and discrepancy resolution
- Familiarity with ICH E6 Good Clinical Practice and FDA 21 CFR Part 11 regulations
- Experience with clinical trial data review across Phase I through Phase III studies
- Strong attention to detail and ability to meet database lock timelines under pressure
Tips for Your Clinical Data Associate Job Search
Tailor your resume to EDC systems
Highlight the specific electronic data capture platforms you've used, such as Medidata Rave, Oracle Clinical, or Veeva Vault. Recruiters scanning clinical data associate applications filter fast, and named systems get attention that generic 'EDC experience' never will.
Apply early to roles that fit
Migrate Mate lists clinical data associate openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Align your CCDM certification strategy
If you're targeting senior clinical data associate roles, earning the Certified Clinical Data Manager credential signals readiness for lead responsibilities. Many job postings list it as preferred, and having it moves your application ahead of candidates with equal experience but no credential.
Read the protocol before your interview
Clinical data associate interviews frequently include scenario questions tied to real data discrepancy or query resolution situations. Reviewing ICH E6(R2) Good Clinical Practice guidelines beforehand lets you answer those scenarios with the precise language hiring managers expect.
Show query resolution volume on your resume
Generic phrases like 'managed clinical data' don't tell a hiring manager much. Describe the scope of your data review work, the therapeutic areas covered, and the types of discrepancies you resolved, so they can picture your day-to-day contribution clearly.
Negotiate start date alongside your offer
CRO and pharma onboarding for clinical data associate roles often involves system access provisioning and training modules that add lead time. Confirming your start date during offer negotiation prevents gaps and signals you understand how clinical operations actually work.
Clinical Data Associate Jobs: Frequently Asked Questions
Which companies are hiring the most clinical data associates?
The companies hiring the most clinical data associates right now include Regeneron, Veeva Systems, and PTC Therapeutics, with the largest share of openings in New Jersey, Massachusetts, and California, based on current listings on Migrate Mate as of November 2026. CROs and large pharmaceutical companies tend to post the highest volume of openings year-round.
How many clinical data associate jobs are remote?
About 69% of clinical data associate openings are fully remote or hybrid as of November 2026, reflecting how much of the role centers on EDC platform work rather than on-site activity. Remote options are most concentrated in data review, query management, and database lock support, while site monitoring-adjacent roles more often require some travel or on-site presence.
How do you become a clinical data associate?
Start with a bachelor's degree in a life sciences, health informatics, or statistics field, then build hands-on familiarity with at least one major EDC platform through coursework, an internship, or a junior data operations role. Earning a certification in clinical data management strengthens your candidacy for mid-level positions. Most employers also want demonstrated experience with GCP guidelines and clinical trial documentation before promoting candidates into independent data review responsibilities.
Can you get a clinical data associate job with little experience?
Yes, entry-level clinical data associate roles exist specifically for candidates coming from academic research, clinical operations, or health informatics backgrounds without direct CDA experience. Emphasizing transferable skills like database accuracy, discrepancy tracking, or regulatory document handling helps close the gap. Some CROs and staffing organizations run structured associate programs that pair new hires with experienced CDAs before assigning independent data review responsibilities.
What does the clinical data associate interview process look like?
Most clinical data associate interviews include an initial recruiter screen focused on EDC platform familiarity and therapeutic area background, followed by a technical interview with the data management team. That second stage typically involves scenario questions on query resolution, discrepancy handling, and GCP compliance. Some employers add a practical exercise where candidates review a sample dataset or annotated case report form and walk through how they'd flag and resolve issues.
Where can I find and apply to clinical data associate jobs?
You can find and apply to clinical data associate jobs on Migrate Mate, which lists current openings from across the United States. Search the listings to find roles that match your experience level, therapeutic area focus, and location preference, then apply directly to each one that fits.
See All 19 Clinical Data Associate Jobs
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