Novartis

Pharmaceutical

ClinicalResearchAssociateIII

₹25–45L ~AI est. Brazil FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Clinical Research Associate III at Novartis. Skills: Clinical Research, Site Management, Protocol Compliance. Build partnerships with clinical trial sites. Serve as primary point of contact”

Industry & Context.

Pharmaceutical
Problems you'll solve

Risk-based decision-making; Problem solving

Eligibility Requirements

Travel approximately fifty percent

What They're Looking For.

Must Have

Bachelor’s degree in a scientific, healthcare, or related field, At least five years of clinical research experience, site monitoring and site management experience, knowledge of clinical trial processes, knowledge of ICH and GCP guidelines, Understanding of global regulatory expectations, Demonstrated ability to manage multiple study sites independently, communication and stakeholder management skills, analytical thinking and risk-based decision-making skills

Nice to Have

pharmaceutical or biotechnology settings experience

What You'll Do.

Build partnerships with clinical trial sites

Serve as primary point of contact

Manage assigned sites across trials

Ensure compliance with study plans

Ensure compliance with regulatory requirements

Lead site initiation visits

Train site teams on protocol expectations

Train site teams on protocol updates

Conduct remote monitoring activities

Conduct on-site monitoring activities

Support subject safety

Support protocol compliance

Evaluate site performance proactively

Implement mitigation plans

Address quality concerns

Drive early site engagement

Conduct feasibility activities

Plan patient identification

Maintain complete study documentation

Maintain accurate study documentation

Maintain investigator site files

Maintain trial master file updates

Support inspection readiness

Follow up on corrective actions

Identify operational improvement opportunities

Work with sites to strengthen study execution

Share expertise on complex trials

Provide guidance to colleagues

Provide mentorship to colleagues

How You'll Work.

Team & Collaboration

Cross-functional teams; Study teams

Communication Scope

Stakeholder management

Process & Methodology

Clinical Trial Management

Full Job Description

**Job Description Summary** Job Title: Clinical Research Associate III #LI-Remote Location: Remote role in Brazil About the Role Make a meaningful difference in the future of medicine. As a Clinical Research Associate III, you will play a critical role in delivering high-quality clinical trials that help bring innovative therapies to patients faster. In this site-facing position, you will build trusted partnerships, lead monitoring excellence across complex studies, and help ensure the highest standards of patient safety, regulatory compliance, and data integrity. If you are energized by ownership, collaboration, and the opportunity to influence outcomes across global clinical research, this is a role where your expertise can truly make an impact. **Job Description** **Key Responsibilities** * Build strong partnerships with clinical trial sites and serve as the primary point of contact throughout study delivery * Manage assigned sites across Phase One to Phase Four trials in line with study plans and regulatory requirements * Lead site initiation visits and ensure site teams are fully trained on protocol expectations and updates * Conduct remote and on-site monitoring activities to support data quality, subject safety, and protocol compliance * Evaluate site performance proactively and implement mitigation plans to address risks, delays, or quality concerns * Drive early site engagement through feasibility activities and patient identification planning with study teams * Maintain complete and accurate study documentation, including investigator site files and trial master file updates * Support inspection readiness through audit preparation, issue resolution, and follow-up on corrective actions * Identify operational improvement opportunities and work with sites to strengthen study execution * Share expertise on complex trials and provide guidance and mentorship to less experienced colleagues **Essential Requirements** * Bachelor’s degree in a scientific, healthcare

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