Senior Clinical Research Associate

Natera

Senior Clinical Research Associate at Natera executing clinical studies from concept to completion in oncology and women's health. Collaborating with cross-functional teams to ensure compliance and quality metrics.

Posted 7/30/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $99,400 - $124,200 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical study operations, including logistical support, budget management, and compliance with regulatory standards. Proficient in developing study-related documents and training stakeholders while ensuring adherence to SOPs and ICH-GCP guidelines.

Highest-signal resume keywords

Clinical Study ManagementClinical EDC SystemsTrial Master File (TMF) FamiliaritySOPs and ICH-GCP ComplianceBudget and Contract Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study OperationsBudget ManagementClinical Documentation ManagementCase Report Form DesignBio Sample ManagementAnalytical Problem SolvingProject LeadershipTime ManagementDetail OrientationWriting Skills

Soft Skills

Interpersonal SkillsCommunication Skills

Tools & Technologies

MS WordMS ExcelMS PowerPoint

Industry Keywords

Clinical TrialsBiopharmaDiagnosticsMedical DevicesFDA Regulations

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide high level logistical support for clinical study operations.
Develop study-related documents with minimal Clinical Trial Manager guidance.
Manage small to medium size study contracting, budget, invoicing and payment process for all clinical trial vendors.
Support the Clinical Data Management team in the design and content of case report forms, including support and testing of an EDC.
Manage the preparation, handling, filing, and archiving of clinical documentation and reports.
Oversee clinical trial supplies related to biospecimen collection, processing, shipment, and storage.
Train CROs, vendors, investigators, and study coordinators on study requirements.
Monitor and track clinical trial progress, provide status updates to stakeholders.
Develop new study monitoring plans and monitor studies following those plans.
Perform study activities including consent participants for research studies.
Update Clinical Department SOPs with guidance from CTM and/or Director.
Partner with other research and development groups at Natera.

Requirements

What you’ll need

BA/BS degree in life sciences, related field, or equivalent.
Minimum of 4 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields.
Experience with clinical EDC systems.
Familiarity with the organization and structure of the Trial Master File (TMF).
Familiarity with bio sample management, sample processing, and biobanking best practices.
Competency in SOPs, ICH-GCP, FDA Regulations.
Proficiency in MS Word, Excel and PowerPoint.
Demonstrated ability to work independently and lead projects.
Demonstrated analytical skills and ability to identify complicated problems and propose solutions.
Strong interpersonal skills and communication skills (both written and oral).
Excellent writing skills.
Detail oriented, with solid organization and time management skills.

Benefits

Comp & perks

Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
Free testing for Natera employees and their immediate families.
Fertility care benefits.
Pregnancy and baby bonding leave.
401k benefits.
Commuter benefits.
Employee referral program.