Senior Clinical Research Associate

Novartis

. Manage trusted site relationships and perform on-site and remote monitoring activities for Phase I–IV clinical trials .

Posted 11/6/2026full-timeRemote • United StatesSenior💰 $108,500 - $201,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial site relationships and ensuring compliance with ICH/GCP and local regulations. Proficient in site monitoring, risk identification, and collaboration with cross-functional teams to enhance study execution.

Highest-signal resume keywords

Site Monitoring ExperienceKnowledge Of GCP/ICH StandardsClinical Trial ManagementStrong Communication SkillsProblem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial MonitoringSite ManagementData Integrity AssuranceRegulatory ComplianceRisk IdentificationProtocol ComplianceTraining Site PersonnelDocument PreparationStudy ExecutionOncology Experience

Soft Skills

Negotiating SkillsTime ManagementPresentation Skills

Industry Keywords

Drug Development ProcessPhase I–IV TrialsAudit ReadinessCorrective Action ImplementationCross-Functional CollaborationSSU CRA PartnershipTravel Willingness

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Manage trusted site relationships and perform on-site and remote monitoring activities for Phase I–IV clinical trials
Support trial initiation, conduct, and timely completion in compliance with ICH/GCP, local regulations, SOPs, and monitoring procedures
Serve as the primary site manager and first point of contact between site staff and Novartis
Support collaboration, milestones, and deliverables as a frontline liaison
Manage assigned sites and networks according to monitoring plans and Novartis procedures
Conduct site initiation visits and provide ongoing training for site personnel
Perform continuous on-site and remote monitoring for protocol, GCP, regulatory, and process compliance, data integrity, and patient safety
Facilitate preparation and collection of site- and country-level documents
Identify risks, resolve issues, and escalate concerns as needed
Collaborate with cross-functional teams to drive efficient study execution and process improvements
Deliver timely, high-quality, robust, reliable site data supporting Trial Monitoring goals
Partner with SSU CRA for seamless transition of site responsibility
Act as a subject matter expert across study activities when required
Support audit and inspection readiness activities and corrective action implementation

Requirements

What you’ll need

Minimum of 3 years’ experience in site monitoring
BS/BA degree in Scientific, Healthcare or related field
Excellent knowledge of the drug development process, specifically clinical trial/research
Knowledge of international standards (GCP/ICH, FDA, EMEA)
Ability to manage multiple priorities and manage time efficiently
Excellent site management capabilities with demonstrated negotiating and problem-solving skills
Strong communicator and presentation skills (oral and written)
Fluent in both written and spoken English
Must have a fully valid and unrestricted driver’s license
Willingness and ability to travel by plane or car up to 80% of the time
RLT, CAR T or Oncology experience a plus

Benefits

Comp & perks

Performance-based cash incentive
Eligibility to be considered for annual equity awards, depending on role level
Health benefits
Life benefits
Disability benefits
401(k) with company contribution and match
Vacation
Personal days
Holidays
Other leaves
Reasonable accommodations for qualified individuals with disabilities