Associate Manager, Clinical Data Management

CRISPR Therapeutics; Boston (MA); Hybrid; USD 100,000 - 115,000; Full time

Job summary

CRISPR Therapeutics is seeking an Associate Manager of Clinical Data Management to support data management activities across all stages of clinical drug development. You will work with cross-functional teams to ensure accurate, complete data, handling data review, queries, reconciliation, and vendor data.

The role also covers documentation, UAT, and GCP inspection readiness. The position requires 4–6+ years of CDM experience, familiarity with Medidata Rave, Veeva, and CDISC standards, plus

Qualifications

• Bachelor’s Degree in a health‑related field.
• 4–6+ years of clinical data management experience.
• 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 of 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.

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.

Skills

CDM experience

EDC systems

Data reconciliation

UAT testing

Vendor management

Data querying

CDISC/SDTM/CDASH

Medidata Rave

Veeva

J-Review / reporting tools

Education

Bachelor’s Degree in a health-related field

Tools

Medidata Rave

Veeva

J-Review

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.

Job Description

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