N-Power Medicine, Inc.

N-Power Medicine is transforming oncology drug development through an innovative, always-on clinical research system that integrates research into routine care. Their unique approach accelerates…

AIClinical TrialsCommunity ResearchData PrivacyDrug DevelopmentHealthcare InnovationOncologyPatient Engagementnpowermedicine.com

N-Power Medicine, Inc.

N-Power Medicine is transforming oncology drug development through an innovative, always-on clinical research system that integrates research into routine care. Their unique approach accelerates…

AIClinical TrialsCommunity ResearchData PrivacyDrug DevelopmentHealthcare InnovationOncologyPatient Engagementnpowermedicine.com

HQRedwood City, US

Team Size117

Open Jobs1

Total Funding-

Latest Fundraise2 years ago

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Clinical Research Operations Specialist

RemoteUS

Remote • US

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About N-Power Medicine

N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.

Position Overview

We are seeking an experienced and adaptable Clinical Research Operations Specialist to oversee the planning, implementation, and management of oncology clinical trials across multiple trial sites within the N-Power Network. This role serves as a key operational bridge between internal teams, trial site personnel, and external pharma or CRO partners, ensuring streamlined communication, executional excellence, and a superior experience for all stakeholders. This role will proactively identify potential barriers to successful implementation of the trial work plan and develop strategic solutions to mitigate those challenges, while driving efficient resource allocation, regulatory and protocol adherence, and timely delivery of study milestones.

This customer-facing role requires expertise in clinical trial management, site operations, stakeholder engagement, and process optimization. This is a highly visible and impactful position within a dynamic, rapidly evolving organization—ideal for someone who excels at creative problem solving, thrives in ambiguity, and brings both rigor and flexibility to clinical trial operations.

This position is remote within the United States.

Role Objectives and Responsibilities

Trial Execution & Oversight

Compliance & Quality Assurance

Ensure all trial activities comply with Good Clinical Practice (GCP), Institutional Review Board (IRB) guidelines, FDA regulations, and health system policies.
Work closely with other N-Power teams to support submissions, audits, and inspections.

Performance & Reporting

Track key performance indicators (KPIs) related to trial enrollment, retention, protocol adherence, and data integrity.
Provide regular updates and reports to senior leadership, sponsors, and other key stakeholders.
Utilize data-driven insights to recommend operational improvements and enhance trial efficiency.

Education, Experience, Behavioral Competencies, & Skills

Travel Requirements

Ability to travel, up to 10%, may be required

Pay Information

The expected salary range for this position is $108,000 and $143,000. 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.

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.”

We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Covid-19 Policy – The Company is committed to providing and maintaining a safe workplace, and to safeguard the health and well-being of our employees, families, visitors, and the community. While vaccination remains one of the most important tools in advancing the health and safety of employees and promoting the efficiency of workplaces, we are now in a different phase of our response when these measures are no longer necessary. We currently do not have mandatory COVID-19 vaccination requirements for our employees and contractors, as the COVID-19 public health emergency has ended. However, there are certain N-Power Medicine employees and contractors who, based on their role, will be required to continue to follow our 2021 COVID-19 vaccination and other requirements as mandated by N-Power Medicine’s partners they serve. We reserve the right to modify or amend our corporate policy at any time.

Applicants must be currently authorized to work in the U.S. on a full-time basis. The Company will not sponsor applicants for work visas.

Notice on fraudulent job offers: Only positions posted on https://npowercareers.multiscreensite.com/ site are legitimate. Please be mindful of recruitment fraud and job scams.

Oversee the end-to-end implementation and execution of assigned oncology studies across multiple Network sites, ensuring compliance with study protocols, timelines, and regulatory requirements.

Act as a strategic liaison between pharma sponsors, contract research organizations (CROs), clinical sites, and internal teams to ensure alignment and execution of study objectives.

Proactively identify operational risks and implement creative, timely solutions (SOPs, tools, and best practices) to optimize clinical trial workflow, patient recruitment, and data quality.

Collaborate with regulatory, data, quality, and site teams to ensure compliance with applicable regulations and internal SOPs.

Monitor trial progress, identify bottlenecks, and proactively address identified operational challenges.

Review and provide input on essential study documents (e.g., protocols, informed consents, site training materials).

Oversee trial-specific training for internal stakeholders and site teams.

Responsible for operational input and oversight in designing, planning, initiating and completing clinical trials across assigned disease teams.

Lead clinical study and cross functional team to make key decisions related to strategy and issue resolution.

Participate in initiatives to establish best practices for optimizing patient enrollment in clinical trials.

Collaborate with stakeholders to develop and implement trial specific training programs.

Innovate and implement novel patient enrollment strategies to maximize clinical trial participation.

Identify and integrate new tools, workflows, and methodologies to improve protocol implementation and patient enrollment processes.

Perform additional duties and responsibilities as required.

5+ years in clinical trial operations, with experience in a health system setting preferred.

Bachelor’s degree in life sciences, healthcare administration, or a related field required; Master’s degree (MPH, MBA, MS) or clinical background (RN, PharmD) preferred.

2+ years in oncology clinical trial experience preferred.

Strong understanding of clinical research protocols, regulatory requirements, and site management best practices.

Exceptional project management and organizational skills.

Strong interpersonal and relationship-building abilities.

Ability to manage multiple priorities in a fast-paced environment.

Proven ability to navigate highly matrixed environments, managing multiple stakeholders and priorities.

Strong track record of successfully executing projects under tight timelines.

Exceptional interpersonal and communication skills, with the ability to engage and influence senior stakeholders, clinical teams, and technical experts.

Demonstrated ability to inspire teams, foster collaboration, and drive meaningful impact in clinical research.

Prior experience in management or leading cross functional teams is desirable.

Generous, Curious and Humble.