Paralegal

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🕒 5 days ago

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Logo of K2 Medical Research

K2 Medical Research

201 - 500 employees

Founded 2021

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 Private equity on 2024-07

Healthcare • Biotechnology • Pharmaceuticals

K2 Medical Research is a privately-owned clinical research facility with multiple locations in Florida, Tennessee, and Rhode Island. It specializes in conducting multiphasic clinical trials to evaluate new and innovative medical treatments while prioritizing participant safety and privacy. K2 focuses on a range of therapeutic areas including genetic and biomarker testing, memory assessments and Alzheimer’s disease, mental health (anxiety, depression), metabolic conditions (NASH/fatty liver disease, diabetes), migraines, vaccines, and related clinical research aimed at advancing treatments and connecting patients with investigational therapies.

📋 Description

• Assist Corporate Counsel in drafting, reviewing, and formatting standard agreements (including: Clinical Trial Agreements (CTAs); Confidentiality Agreements (NDAs); Master Services Agreements (MSAs); Vendor and service agreements; Investigator agreements and site agreements) • Facilitate the execution and routing of contracts with pharmaceutical sponsors, CROs, research sites, and vendors • Track contract status, manage legal documentation, and maintain an organized and up-to-date contract lifecycle management system • Ensure all executed agreements and related documentation are properly filed and accessible • Help develop, organize, and maintain contract templates, playbooks, and standard operating procedures • Support cross-functional collaboration to facilitate document flow and approvals • Conduct basic legal research and gather information on healthcare regulatory and operational matters

🎯 Requirements

• Associate’s degree, Bachelor’s degree, or Paralegal Certificate from an ABA-approved program • 1–3 years of relevant paralegal, legal assistant, or contract administration experience • Strong proficiency in reviewing, proofreading, and formatting contracts and legal documents • Excellent written and verbal communication skills • Highly organized with exceptional attention to detail and the ability to manage multiple priorities simultaneously • Preferred: Experience in healthcare, life sciences, clinical research, or commercial contracting • Familiarity with clinical trial agreements, HIPAA, and FDA regulatory frameworks • Experience managing contract databases or lifecycle management software in a fast-paced environment

🏖️ Benefits

• Health insurance • Dental options • Vision options • Supplemental insurance plans • 401(k) with immediate employer match • Generous paid time off • Paid holidays • Four-day work week with 10-hour shifts

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