Everest Clinical Research
501 - 1000 employees
Founded 2004
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
Pharmaceuticals • Biotechnology • B2B
Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.
Site Contracts Specialist II
Job not on LinkedIn
🕒 July 11
🏖️ New Jersey – Remote
💵 $70k - $85k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Contracts Specialist
🦅 H1B Visa Sponsor
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Everest Clinical Research
501 - 1000 employees
Founded 2004
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
Pharmaceuticals • Biotechnology • B2B
Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.
📋 Description
• supporting the site start up process of clinical studies by negotiating and executing Clinical Trial Agreements and their budgets • ensuring the quality and timeliness of negotiations • conducting timely site follow ups and contacting sites every few business days • raising any changes in site circumstances as they arise • negotiating study-specific CDAs, CTAs, Amendments or other related documents • tracking all site interaction in a timely and accurate manner • escalating any issues to the Site Contract Manager and study team as necessary
🎯 Requirements
• Bachelor’s degree or international equivalent in a related field such as science/biology or English/communication; Master's or JD preferred • 2+ years of investigative site contracting experience with both the legal language and the budget.
🏖️ Benefits
• medical, dental, and vision coverage • life & AD&D insurance • short- and long-term disability • tuition reimbursement • fitness reimbursement • employee assistance program (EAP) • pension plan • generous paid time off and sick leave • opportunity to earn a performance based bonus
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