Associate Director, Clinical Operations

N-Power Medicine, Inc.

Associate Director responsible for clinical operations in drug development at N-Power Medicine. Collaborating with cross-functional teams to ensure efficient execution of clinical trials.

Posted 7/31/2026full-timeRedwood City • California • 🇺🇸 United StatesSenior💰 $175,000 - $195,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading clinical trial operations, including strategic planning, regulatory compliance, and data analysis. Proven ability to manage project plans, budgets, and cross-functional collaboration in a fast-paced environment.

Highest-signal resume keywords

Clinical Trial ManagementRegulatory ComplianceProject ManagementTeam LeadershipData Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical OperationsProgram ManagementStudy Protocol DevelopmentRisk Mitigation StrategiesBudget ManagementEDC SystemsCTMS SystemsCTFM SystemsETMF SystemsGlobal Regulatory Requirements

Soft Skills

Strong CommunicationInterpersonal SkillsProblem SolvingAdaptabilityCollaboration

Industry Keywords

BiotechnologyHealthcareLife SciencesOncology Clinical ResearchICH GCPUS CRFSOPs

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and oversee the strategic planning, implementation and execution of clinical trials and external control arms across multiple programs
Develop and manage comprehensive program project plans, including study protocols, clinical trial budgets, timelines, and risk mitigation strategies
Collaborate cross functionally with internal teams to ensure alignment on clinical trial objectives and milestones
Serve as the point of contact for clinical suppliers, ensuring adherence to contractual agreements and quality standards
Ensure compliance with regulatory requirements and company SOPs throughout all stages of clinical trial conduct
Oversee the collection, analysis and interpretation of clinical trial data
Hire, train and develop the Clinical Operations team

Requirements

What you’ll need

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
Must be comfortable working in a fast-paced environment

Benefits

Comp & perks

equity at hire
discretionary annual bonus based on Company performance
company benefits
401K plan
flexible work environment
competitive industry benefits