Director of Clinical Research Consulting

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August 5

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Vitalief Inc.

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B2B • Healthcare Insurance • Pharmaceuticals

Vitalief Inc. is a company dedicated to transforming the clinical trial landscape by improving the value and contribution of trial sites throughout the drug development lifecycle. They specialize in offering consulting services, functional service provision (FSP), and workforce solutions to streamline clinical trials, enhance patient outcomes, and deliver value for Sponsors, Contract Research Organizations (CROs), and sites. With a focus on site operations and patient care in the life sciences, Vitalief serves academic sites, community health systems, independent sites, site networks, sponsors, and CROs. Their services address challenges in research and clinical trials, providing end-to-end solutions like strategic planning, resourcing models, training, and operational solutions. Vitalief is committed to delivering more efficient, high-quality clinical trials and driving innovation in the research industry.

51 - 200 employees

🤝 B2B

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $2M Venture Round on 2023-04

📋 Description

• You represent the pinnacle of consulting success by creating a high-performance environment. • Ensure Vitalief’s success and shape the industry through strong leadership and unmatched industry expertise. • Provide strategic planning and project oversight accelerating our client’s Study Activation through best-in-class project management. • Help clients evolve and adapt to the rapid demands of the research and clinical trials environment. • Perform the Study Activation functions including contract negotiation and budget preparation. • Take a lead role in developing long-standing relationships with clients to meet business objectives. • Provide sales support and work closely with talent acquisition team.

🎯 Requirements

• Bachelor’s degree in related discipline, preferably in life science, healthcare or equivalent qualification. • 10 or more years of Healthcare and/or Clinical Research industry experience. • 2 years of experience and fluent in all activities required for preparing a clinical trial for Site Activation. • Hands-on experience completing various study start-up activities. • Demonstrated experience in devising/implementing processes and tools to accelerate the study start-up process. • Any Organizational Change Management (OCM) experience and formal training is a huge plus. • Dynamic leader with strong executive presence, excellent negotiation skills. • Excellent verbal and written communication and presentation skills. • Delivery team leadership experience including team design and performance management.

🏖️ Benefits

• Competitive compensation program including base salary, bonus, and equity incentives!