
201 - 500 employees
Founded 2018
🏥 Healthcare
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $2.9M Venture Round on 2022-05
Healthcare • Healthcare Insurance • Pharmaceuticals
Headlands Research is a multinational integrated clinical trial site organization that focuses on large-volume recruitment and retention of diverse, inclusive populations through extensive site databases and physician partnerships. With over 5,000 clinical trials successfully completed and a dedicated team of clinical research professionals, Headlands Research is committed to advancing innovative medical therapies to improve lives in various therapeutic areas, including CNS, mental health, and vaccines.
🔥 0 minutes ago
🇺🇸 United States – Remote
💵 $65k - $75k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🏛️ Architect
🚫👨🎓 No degree required
👻 Ghost score 0%
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201 - 500 employees
Founded 2018
🏥 Healthcare
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $2.9M Venture Round on 2022-05
Healthcare • Healthcare Insurance • Pharmaceuticals
Headlands Research is a multinational integrated clinical trial site organization that focuses on large-volume recruitment and retention of diverse, inclusive populations through extensive site databases and physician partnerships. With over 5,000 clinical trials successfully completed and a dedicated team of clinical research professionals, Headlands Research is committed to advancing innovative medical therapies to improve lives in various therapeutic areas, including CNS, mental health, and vaccines.
• Create eSource for new studies according to protocol specifications • Distribute eSource to applicable sites and collaborate with local staff to implement site-specific eSource requirements • Serve as a subject matter expert for eSource creation and mentor clinical sites • Develop template logs, including AE and deviation logs, within the eSource environment for consistent centralized reporting • Communicate with Finance, QA, Sites, and other teams to ensure eSource fulfills all requirements • Provide extensive organizational training to ensure staff are trained and competent in eSource development • Oversee and manage eSource creation
• 2+ years of clinical research experience (CRC, QA, Source, CRA) required • 2+ years of ICH/GCP guidelines and FDA regulations knowledge from hands-on work experience required • BA/BS degree preferred • Familiar with medical terminology • Demonstrated proficiency in Microsoft Office (Word, Excel, PowerPoint, and Outlook) • Demonstrated ability to think strategically and be the leader of change • Ability to build effective working relationships and collaborate within the organization • Problem-solving, goal-oriented, and team-player approach • Excellent verbal and written communication skills
• Competitive pay + annual performance incentives • Medical, dental, and vision insurance • Health Savings Accounts (HSA) • Flexible Spending Accounts (FSA) • 401(k) plan with company match • Paid time off (PTO) and company holidays • Disability, accident, and life insurance options • Mission-driven culture focused on advancing medicine and improving patient outcomes
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