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Senior Director, Clinical Operations

🏒 Avirmax Biopharma Inc. βœ“ Verified Direct Employer
πŸ“ Hayward, CA ⚑ Direct Opportunity πŸ•’ Today
Work Model
πŸ“ Hayward, CA
Employment
πŸ’Ό Full-Time Direct
Recruitment Type
πŸ›‘οΈ Direct to HR Pipeline
πŸ›‘οΈ
Verified Direct Employer Opening: You are submitting directly to Avirmax Biopharma Inc.'s recruitment pipeline with zero intermediary fees.

Role Overview & Responsibilities

Job Title: Senior Director, Clinical Operations

Avirmax Biopharma, Inc. (ABI) based in San Francisco Bay Area, is a preclinical stage biopharmaceutical company focusing on innovation and development of genetic medicines to treat chronic and degenerated ocular diseases using integrated solutions in engineering and optimization of adeno-associated virus (AAV) vectors, rich experience and knowledge in biopharmaceutical development and product supply. Our mission is to deliver patients with safe, effective, durable, affordable and accessible AAV-mediated biotherapeutics to preserve patient’s vision.

Job Description:

We are seeking a highly experienced Senior Director, Clinical Operations to be a part of our rapidly growing team at Avirmax. The Senior Director will lead cross functional teams, including internal and third party, to drive clinical development activities for the CRO/CDMO. This position will use project management methodologies and best practices to help deliver projects on time and within budget, including establishment of SOPs

Responsibilities:(including, but not limited to):

  • Leading clinical teams, project and trial planning, budgeting and financial oversight, staff and contract research organization (CRO) management, program/trial clinical operation, timelines and GCP compliance

· Plan and implement projects, help define project scope, goals, deliverables; and define tasks and required resources.

  • Ensure that clinical trials are properly resourced, managed and executed in accordance with timelines and good quality practices.
  • Collaborate closely with the key stakeholders of the project.
  • Review master service agreements, statements of work, and quality agreements relating to clinical operations
  • Manage budget, allocate project resources, create schedule and project timeline, track deliverables and monitor and report on project progress.
  • Plan clinical headcount and hiring needs to meet program workload demands.
  • Maintain Shared File System and other databases with project status and key project information.
  • Participate in developing and providing input to protocols, annual safety reports, clinical study reports, publications/presentations and regulatory submissions
  • Contribute to internal process improvement initiatives, especially those involving tools and knowledge management solutions.

Requirements:

  • 5-10 years applicable experience in clinical operations in ophthalmology pharma/biotech industry.
  • Experience and knowledge of end-to-end management of clinical trial conduct, knowledge of the pharmaceutical industry and an understanding of clinical drug development, clinical trials operations and regulatory components is essential
  • A thorough understanding of drug development from IND to NDA

· Knowledge and experience with developing, negotiating and managing contracts (vendor and site)

  • Regulatory inspection experience
  • Strong working knowledge of FDA, EMA, PMDA regulations and expectations, Good Clinical Practice, ICH guidelines, and clinical operations best practices
  • Strong communication, organizational and interpersonal skills are necessary for this role
  • Ability to work in a fast-paced environment with a sense of urgency and handle multiple roles.

Education:

  • Minimum of Bachelor's degree or Master’s degree in Business Administration, or related field.

Job Location: Bay Area.

Job Type: Full-time.

Work authorization: work authorization in US is required.

About the Benefits:

The successful candidate will enjoy a competitive base salary and the opportunity to participate in incentive compensation programs including awards and stock option plans. Additionally, Avirmax Biopharma Inc. offers all team members a comprehensive benefits program including medical and dental insurance, 401(k), paid vacation and holiday time.

Avirmax Biopharma Inc. is an equal opportunity employer (EOE/AA)

Job Type: Full-time

Pay: From $120,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Flexible spending account
  • Health insurance
  • Paid time off
  • Parental leave

Schedule:

  • Monday to Friday

Supplemental pay types:

  • Bonus pay

Work Location: Hybrid remote in Hayward, CA

Frequently Asked Questions

How do I apply for the Senior Director, Clinical Operations position at Avirmax Biopharma Inc.?

Click the “Apply for this Position” button on this page to submit your application directly to Avirmax Biopharma Inc.'s HR pipeline without recruitment agency markups.

Is this role eligible for remote work or international relocation?

This position is based in Hayward, CA with potential relocation and visa sponsorship considerations for qualified candidates.

Are there any fees to apply through Jobflixs?

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