Senior Clinical Research Associate – Oncology

🕒 July 10

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 44%

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UBC

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2003

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

UBC is a company dedicated to improving patient outcomes by connecting specialty therapies to patients in need. They provide modern and customized solutions focusing on access, safety, and evidence generation for biopharmaceutical products. UBC specializes in evidence development, risk management, and patient access, utilizing real-world data and innovative technologies to optimize the healthcare journey and ensure effective medication use.

📋 Description

• Monitor clinical trials and observational studies for protocol adherence • Manage site activities and oversee data collection and integrity • Ensure sites conduct studies and report data according to regulations, guidelines, and sponsor requirements • Mentor and train junior-level CRAs • Apply project-specific protocols • Perform remote and on-site monitoring according to project timelines • Schedule travel according to project requirements and UBC travel policy • Submit expense reports within UBC requirements • Attend project team, department, and manager meetings • Complete site monitoring reports and letters with minimal corrections • Follow up on site issues and action items within required timelines • Enter site visits, monitoring reports, follow-up letter dates, and site contacts into UBC’s CTMS • Monitor EDC data entry and assist sites with eCRF resolution • Review Investigator Site Files and perform Investigational Product reconciliation • Maintain regular contact with assigned sites • Complete SOP reviews, training assessments, and documentation on time • Assist project and management teams with mentoring, training, and assessing junior CRAs • Assist with UBC CRA, departmental, and sponsor-specific training presentations • Support Project Manager and Lead CRA with additional tasks • Complete site management and monitoring activities according to project plans and timelines • Perform other assigned duties that may align with other UBC departments

🎯 Requirements

• US-based • 5 years of monitoring experience, including at least 3 years in oncology and some ophthalmology monitoring • Bachelor’s degree – Life Science preferred or equivalent years of industry and clinical research experience • Minimum of 36 months on-site monitoring experience including site selection, initiation, management, and monitoring activities • Comprehensive knowledge of medical terminology and regulatory guidelines • Excellent critical thinking and resolution skills • Excellent written and verbal communication skills in English and local language (as applicable) • Experience working in clinical trials and observational studies preferred • Experience and familiarity with CTMS, eTMF, EDC, Microsoft Office applications • Proven ability to deliver highly accurate work and adhere to deadlines in a fast-paced environment • Travel up to 80% required in the North American region

🏖️ Benefits

• Remote opportunities • Competitive salaries • Growth opportunities for promotion • 401K with company match • Tuition reimbursement • Flexible work environment • Discretionary PTO (Paid Time Off) • Paid Holidays • Employee assistance programs • Medical, Dental, and vision coverage • HSA/FSA • Telemedicine (Virtual doctor appointments) • Wellness program • Adoption assistance • Short term disability • Long term disability • Life insurance • Discount programs