Clinical Operations Lead (On-Site)

South San Francisco, CA

Job Title: Clinical Operations Lead (On-Site)
Location: South San Francisco, CA
Type: Contract
Compensation: $80.57
Contractor Work Model: Hybrid
Hours: 40.0

Overview

Responsibilities

  • Contribute in operational activities that enable trial execution and delivery of the PD portfolio of clinical studies and programs across Disease Areas by providing operational and/or strategic input to the teams.
  • Support local and global initiatives and other duties as assigned according to business needs and priorities.
  • Promote and support quality and compliance by ensuring adherence to GCP/GVP regulations, maintaining data integrity, and applying a balanced risk-based approach.
  • Collaborate across cross-functional teams and geographies to support the development and implementation of clinical operations best practices.
  • Advance digital transformation initiatives by fostering change adoption among investigators and patients.
  • Participate in continuous improvement and change management activities, identifying opportunities for process enhancements and solving complex problems.
  • Develop and execute plans supporting clinical trials and enabling projects with minimal guidance.
  • Build strong relationships with investigators and site staff, positioning the company as a preferred partner in clinical research.

Requirements

  • At least 2 to 5 years of relevant experience in clinical operations or drug development.
  • Knowledge of clinical trial processes, GCP, ICH, and related regulatory guidelines.
  • Ability to thrive in ambiguous, collaborative environments with distributed authority.
  • Strong organizational and problem-solving skills to manage clinical programs and projects efficiently.
  • Effective communication skills; comfortable sharing information transparently and listening actively.
  • Experience supporting clinical trials across multiple geographies; ability to develop subject matter expertise.
  • Ability to work in rapid cycle environments, prioritize tasks, and align priorities with strategic goals.
  • Demonstrated ability to adopt new digital technologies and serve as a change agent.
  • Capable of independently planning and supporting the execution of clinical trials and projects.
  • Proven collaboration skills to work with investigators and clinical staff, fostering strong partnerships.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Type: Contract

Experience: 0

Category: Scientific & Clinical

Contractor Work Model: Hybrid

Brand: Joulé

Shift: On-Site

Compensation Range: 75.00 - 80.57 Per Hour

Job ID: 347718

Date Posted: 03/13/2026

Shortcut: https://jobs.systemone.com/byrvqn

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