Site Care Partner – Oncology

🕒 6 days ago

🏄 California – Remote

🏄 California – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🪙 Affiliate Manager

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Responsible for site start-up, activation, relationship management, recruitment, and quality assurance • Contributes to site selection and provides local intelligence • Ensures site support and resolves issues • Collaborates with various functions to optimize communication • Maintains site quality and patient safety utilizing data analytics • Supports Country Specific Activities for clinical trial implementation • Deploys client site strategies by qualifying and activating assigned sites • Reviews and assesses site qualification outputs for site selection • Maintains knowledge of assigned protocols • Conducts study start-up activities including Site Qualification • Ensures follow up activities’ completion post Site Qualification visit • Partners with the Clinical Research Associate for monitoring readiness • Builds relationships and operational quality at the site

🎯 Requirements

• 5+ years prior experience as a CRA in a clinical research or pharma organization • Oncology monitoring/CRA experience is required • Experience reviewing monitoring reports is required • Demonstrated experience in site management • Demonstrated experience in start-up activities through site activation • Demonstrated experience in conduct and close out activities • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience (at least 5 years’ experience) • Proficiency in local language preferred. English is required

🏖️ Benefits

• Health insurance • 401(k) matching • Flexible working hours • Paid time off