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Job Requirements of Clinical Operations Lead (On-Site):
-
Employment Type:
Full-Time
-
Location:
South San Francisco, CA (Onsite)
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Clinical Operations Lead (On-Site)
Tailored Management Services Inc
South San Francisco, CA (Onsite)
Full-Time
Job Title: Clinical Operations Lead
Location: 1 DNA Way, South San Francisco, CA 94080
Work Model: Hybrid (3 days onsite, 2 days remote)
Duration: 12-Month Contract (Potential for Extension or Conversion)
Pay Rate: $58.15 – $78.90/hr (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
Position Overview
The Clinical Operations Lead will contribute to the execution and delivery of clinical studies across multiple disease areas while ensuring compliance with regulatory requirements and industry standards. This role requires strong operational, problem-solving, and collaboration skills within a matrixed organization.
Key Responsibilities
Required Qualifications
Key Competencies
Location: 1 DNA Way, South San Francisco, CA 94080
Work Model: Hybrid (3 days onsite, 2 days remote)
Duration: 12-Month Contract (Potential for Extension or Conversion)
Pay Rate: $58.15 – $78.90/hr (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
Position Overview
The Clinical Operations Lead will contribute to the execution and delivery of clinical studies across multiple disease areas while ensuring compliance with regulatory requirements and industry standards. This role requires strong operational, problem-solving, and collaboration skills within a matrixed organization.
Key Responsibilities
- Support clinical trial operations by contributing to the execution and delivery of clinical studies across various disease areas.
- Provide operational and strategic input to cross-functional teams involved in clinical development programs.
- Participate in local and global initiatives related to clinical operations and process improvement.
- Ensure compliance with ICH, GCP, GVP, and regulatory guidelines, maintaining data integrity and quality standards.
- Collaborate with internal teams and external partners to optimize clinical trial processes and delivery.
- Contribute to continuous improvement initiatives, identifying opportunities to enhance operational efficiency.
- Support the adoption of innovative technologies and digital solutions in clinical studies.
- Work closely with investigators and clinical site staff to strengthen partnerships and position the organization as a preferred collaborator.
- Assist in managing moderately complex projects, balancing priorities and resources to meet program objectives.
Required Qualifications
- 2–5 years of experience in Clinical Operations, Drug Development, or related fields.
- Understanding of clinical trial processes and drug development lifecycle.
- Knowledge of ICH-GCP and regulatory compliance requirements.
- Strong organizational, analytical, and problem-solving skills.
- Ability to work effectively in cross-functional, matrixed teams.
- Excellent communication and collaboration skills.
- Experience supporting clinical trials or operational projects across multiple regions is preferred.
Key Competencies
- Adaptability in fast-paced and evolving environments
- Strong collaboration and teamwork mindset
- Ability to manage priorities and work in rapid operational cycles
- Continuous improvement and change management mindset
- Commitment to patient-focused clinical research
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