Sr. CTA / CTMA

Meet Life Sciences Ltd.; Sunnyvale (CA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Meet Life Sciences Ltd. in the San Francisco Bay Area seeks a Senior Clinical Trial Management Associate to support planning, execution, and oversight of Phase I–III trials in a fast-paced biotech setting.

You will help ensure studies meet timelines, quality standards, and regulatory requirements, coordinating with sites, CROs, and vendors. The role emphasizes strong organization and communication, with collaboration across Clinical Operations leadership and cross-functional teams.

Qualifications

• Three to five or more years of relevant experience within a pharmaceutical, biotechnology, CRO, clinical research, or healthcare environment.
• Bachelor’s degree in a scientific, healthcare, or related discipline.
• Experience supporting company-sponsored clinical trials is required.
• Previous experience supporting Phase I–III clinical studies.
• Strong knowledge of clinical trial operations and study execution.
• Working knowledge of Good Clinical Practice guidelines, FDA regulations, and other applicable regulatory requirements.
• Ability to support multiple study activities, timelines, and priorities in a fast-paced environment.
• Strong organizational, communication, and problem-solving skills.
• Ability to collaborate effectively with internal cross-functional stakeholders and external partners. Oncology trial experience preferred.

Skills

Clinical trial operations

FDA regulations

GCP guidelines

Cross-functional collaboration

Study execution

Education

Bachelor’s degree

Job description

Senior/Clinical Trial Management Associate, Clinical Operations

Job Type: Full-time
Location: San Francisco Bay Area / Hybrid

Position Summary

A clinical-stage biotechnology company is seeking a passionate, creative, and detail-oriented Senior Clinical Trial Management Associate or Clinical Trial Management Associate to join its Clinical Operations team.

This individual will support the planning, execution, and oversight of Phase I–III clinical trials in an industry setting. The role will work closely with Clinical Operations leadership, cross-functional team members, clinical sites, CROs, and external vendors to help ensure studies are delivered in accordance with established timelines, quality standards, study protocols, Good Clinical Practice, and applicable regulatory requirements.

Qualifications and Experience

• Three to five or more years of relevant experience within a pharmaceutical, biotechnology, CRO, clinical research, or healthcare environment.
• Bachelor’s degree in a scientific, healthcare, or related discipline.
• Experience supporting company-sponsored clinical trials is required.
• Previous experience supporting Phase I–III clinical studies.
• Strong knowledge of clinical trial operations and study execution.
• Working knowledge of Good Clinical Practice guidelines, FDA regulations, and other applicable regulatory requirements.
• Ability to support multiple study activities, timelines, and priorities in a fast-paced environment.
• Strong organizational, communication, and problem-solving skills.
• Ability to collaborate effectively with internal cross-functional stakeholders and external partners.
• Previous oncology clinical trial experience is preferred.

Company Overview

The company is a clinical-stage biotechnology organization focused on developing innovative therapies for patients with serious diseases.

The organization offers a collaborative, entrepreneurial environment where employees can contribute directly to the execution of clinical development programs and the advancement of potentially meaningful new medicines.