
51 - 200 employees
Founded 2008
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🧬 Biotechnology
Pharmaceuticals • Healthcare Insurance • Biotechnology
WEP Clinical is a Pharmaceutical Services Provider that specializes in Drug Development Programs, Treatment Access Solutions, and Market Access and Commercialization. The company focuses on providing critical support throughout the entire drug development and commercialization journey, helping sponsors advance their medicines and improve patient access. WEP Clinical offers services such as clinical trial services, expanded access programs, post-approval named patient programs, and market access consulting, ensuring that much-needed therapies reach patients worldwide.
🔥 0 minutes ago
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51 - 200 employees
Founded 2008
💊 Pharmaceuticals
⚕️ Healthcare Insurance
🧬 Biotechnology
Pharmaceuticals • Healthcare Insurance • Biotechnology
WEP Clinical is a Pharmaceutical Services Provider that specializes in Drug Development Programs, Treatment Access Solutions, and Market Access and Commercialization. The company focuses on providing critical support throughout the entire drug development and commercialization journey, helping sponsors advance their medicines and improve patient access. WEP Clinical offers services such as clinical trial services, expanded access programs, post-approval named patient programs, and market access consulting, ensuring that much-needed therapies reach patients worldwide.
• Collaborate with Clinical Operations to develop site initiation timelines and ensure adherence to project milestones • Prepare and manage site startup documentation, including contracts, informed consent forms, and regulatory submissions • Coordinate with contracts and budget teams to ensure timely execution of site agreements • Assist with the preparation and submission of essential regulatory documents for site activation • Ensure all documents are approved by ethics committees and IRBs before site activation • Track progress of regulatory submissions, site contracts, and essential document collection • Verify site readiness with adequate resources and completed training prior to patient enrolment • Participate in study kick-off and initiation meetings to align expectations and timelines • Troubleshoot activation issues and escalate problems to the Project Manager or CRA when needed • Assist with the setup of study supplies and equipment at the site, including investigational products and lab kits
• Bachelor's Degree (in a health or science field preferred) • 2+ years’ experience in site management, clinical research, or equivalent combination of education, experience, and expertise • Computer literacy and proficiency in Microsoft Office and clinical systems (e.g., EDC,CTMS, eTMF) • Effective verbal and written communication skills • Ability to handle confidential information with complete discretion • Strong organizational skills and attention to detail • Ability and willingness to travel up to 20% of the time • The employee must be able to remain in a stationary position for extended periods.
• Medical, dental, and vision insurance • FSA, HSA • Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance • Group short-term and long-term disability insurance • Group Life Insurance • 401K safe harbor plan and company match • Paid vacation, holiday, sick and volunteer time • Paid maternity & paternity leave
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