Associate Director, Clinical Operations

N-Power Medicine

$175K — $195K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; advanced degree preferred.
  • 8-10 years in clinical operations or program management within biotechnology or healthcare.
  • Expertise in regulatory compliance for clinical research (US CRF and ICH-GCP).
  • Familiarity with EDC, CTMS, CTFM, and eTMF systems.
  • Strong ability to handle multiple competing priorities and changes.
  • Excellent communication and problem-solving skills.
  • Engagement in strategic discussions and executive communication.

Responsibilities

  • Lead strategic planning and execution of clinical trials across multiple programs.
  • Develop and manage comprehensive project plans including study protocols and timelines.
  • Collaborate with internal teams to align clinical trial objectives and milestones.
  • Provide strategic input into Clinical Development Plans to support overall clinical strategy.
  • Serve as the primary contact for clinical suppliers and oversee their performance.
  • Ensure compliance with regulatory requirements during clinical trial conduct.
  • Oversee data collection and interpretation, ensuring accuracy and integrity.

Benefits

  • Hybrid work environment; Bay Area preferred, remote considered.
  • Equity at hire and discretionary annual bonuses based on company performance.
  • Comprehensive benefits package and 401K plan.
  • Opportunity to foster a culture of collaboration and operational excellence.
  • Support for continuous improvement and professional development.
Full Job Description
Position Overview

NPM is looking for an exceptional Associate Director, Clinical Operations with an appetite for hands-on development of clinical study management processes and study execution. As an Associate Director, Clinical Operations at NPM, you will collaborate closely with the Senior Director, Pharma Delivery Operations to play a pivotal role in establishing clinical study management necessary to drive NPM's critical applications in clinical trials and community oncology.

You will work collaboratively with cross-functional teams, including Clinical Science, Compliance, Network Operations, Quantitative Science, and Pharma Delivery Operations to develop processes that support the efficient and effective conduct of clinical studies at our Network Partner sites, from planning to close out.

This is a hybrid role; Bay Area preferred, remote considered for the right candidate.

Role Objectives and Responsibilities

  • Lead and oversee the strategic planning, implementation and execution of clinical trials and external control arms across multiple programs in accordance with project timelines, budget, and quality standards
  • Develop and manage comprehensive program project plans, including but not limited to, study protocols, clinical trial budgets, timelines, enrollment and risk mitigation strategies
  • Collaborate cross functionally with internal teams, including Clinical Science, Compliance, Network Operations, Quantitative Science, and Pharma Delivery Operations to ensure alignment on clinical trial objectives and milestones
  • Provide operational expertise and strategic input into the development of Clinical Development Plans (CDP), supporting the overall clinical strategy for the program
  • Serve as the point of contact for clinical suppliers, overseeing their performance and ensuring adherence to contractual agreements, timelines and quality standards
  • Ensure compliance with regulatory requirements, ICH-GCP requirements, and company SOPs throughout all stages of clinical trial conduct
  • Oversee the collection, analysis and interpretation of clinical trial data, working closely with Clinical Science, and Quantitative Science teams to ensure data accuracy and integrity
  • Oversee the eTMF, ongoing quality review and final reconciliation of study documents including review of site regulatory documents/packages
  • Oversee the development and execution of NPM's biospecimen and imaging programs
  • Contribution to the development of clinical trial management best practice processes and SOPs
  • Hire, train and develop the Clinical Operations team, fostering a culture of collaboration, accountability, continuous improvement, and operational excellence


Education, Experience, Behavioral Competencies, & Skills

  • Bachelor's degree required; advanced degree in business, life sciences, or related field preferred
  • 8 - 10 years of experience in clinical operations, delivery/program management, or client operations within biotechnology, healthcare, life sciences, or oncology clinical research
  • Expertise in global regulatory and compliance requirements for clinical research, including but not limited to US CRF and ICH GCP
  • Experience working with EDC, CTMS, CTFM, and eTMF systems preferred
  • Ability to manage multiple competing priorities and adapt to changes
  • Strong communication, interpersonal, and problem solving skills
  • Able to engage in strategic business discussions and craft executive-level communications and materials.
  • Must be comfortable working in a fast-paced environment
  • Generous, Curious & Humble


Travel Requirements

  • Up to 10% of time required to travel in role to support NPM site personnel, attend Face to Face company wide meetings


Pay Information

The expected salary range for this position is $175,000 and $195,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance. This position is eligible for company benefits.

More About Us:

We are a mission-driven, well-funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company "perks."

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