Hybrid Clinical Trial Associate

CRISPR Therapeutics; Boston (MA); Hybrid; USD 85,000 - 95,000; Full time

Job summary

CRISPR Therapeutics in Boston, MA, is seeking a Clinical Trial Associate to support daily clinical trial execution in accordance with GCP and SOPs. You will help coordinate documents and ensure quality control across eTMF and project communications.

The ideal candidate has 1–3+ years in clinical research, strong organization, and proficiency with MS Office tools. This role offers a blend of on-site collaboration with flexible work arrangements in a dynamic biopharma environment.

Qualifications

• BS/BA degree or equivalent and 1–3+ years in clinical research.
• Knowledge of drug development, clinical operation processes and documentation.
• Knowledge of Good Clinical Practice (GCP) and CFR requirements.
• Experience with eTMF; ability to file documents.
• Effective communication, organizational and interpersonal/team skills.
• Proficient in MS Excel, Word and PowerPoint.
• Ability to prioritize and manage multiple tasks and timelines.
• Experience in inter-departmental workgroups to improve processes.

Responsibilities

• Maintain tracking systems and tools for clinical study lifecycle.
• Collect trial information and share with project team, CRO and stakeholders.
• Coordinate study meetings, materials and agendas; record decisions and actions.
• Prepare internal meeting agendas and minutes as applicable.
• Update and quality-control eTMF, SharePoint, and shared drive.
• Track clinical specimen management and vendor relationships.
• Coordinate document version control and prioritize tasks.
• Assist in coordination of regulatory documentation and packaging.

Skills

MS Excel

MS Word

PowerPoint

Communication

Organizational skills

Education

BS/BA degree or equivalent

Tools

eTMF

SharePoint

Job description

CRISPR Therapeutics in Boston, MA, is seeking a Clinical Trial Associate to support daily clinical trial execution in accordance with GCP and SOPs. You will help coordinate documents and ensure quality control across eTMF and project communications.

The ideal candidate has 1–3+ years in clinical research, strong organization, and proficiency with MS Office tools. This role offers a blend of on-site collaboration with flexible work arrangements in a dynamic biopharma environment.