Feasibility Engagement, Manager

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Clinitiative Health Research

WebsiteLinkedInAlle Stellen

11 - 50 Mitarbeiter

Gegründet 2008

⚕️ Krankenversicherung

💊 Pharmazie

🧬 Biotechnologie

Healthcare Insurance • Pharmaceuticals • Biotechnology

Clinitiative Health Research ist ein globales, in den USA ansässiges Netzwerk für klinische Forschung, das sich auf klinische Studien spezialisiert hat. Das Unternehmen verbindet klinische Forschungsstandorte mit Sponsoren und Vertragsforschungsorganisationen (CROs), um erfolgreiche klinische Studien zu erleichtern und hilft den Standorten, durch ein reichhaltiges Angebot an Möglichkeiten an mehr klinischen Studien teilzunehmen. Mit einem Fokus auf maßgeschneiderte Studienmöglichkeiten und Geschäftsentwicklungsdienstleistungen unterstützt Clinitiative seine Partnerstandorte bei Machbarkeitsbewertungen, Standortauswahl und Interessenvertretung für die Sicherung von Studienaufträgen. Ihr umfangreiches Netzwerk deckt verschiedene therapeutische Bereiche ab und zielt darauf ab, den Verbindungsprozess zwischen Forschungsstandorten, Sponsoren und CROs zu optimieren. Clinitiative ist stolz auf seine hohe Bindungsrate und wiederkehrende Zusammenarbeit, was ihr Engagement für das Wachstum und den Erfolg ihrer Partnerstandorte und Sponsoren betont.

Beschreibung

• Job Overview: The Feasibility Engagement, Project Manager will oversee all aspects of the site selection process, deliver site network and individual site capabilities, and serve as a liaison between our Sponsor and CRO partners, internal teams, and respective clients. This role is essential for managing the process flow of study opportunities, ensuring a steady influx of relevant studies for our network, and positioning our clients to maximize their probability of increased study awards. • Key Responsibilities: • - Site Selection Management: Manage the site selection process, ensuring thorough evaluation and optimal placement of sites for clinical trials. • - Capability Delivery: Deliver detailed site network and individual site capabilities, showcasing unique strengths and experiences, especially in diversity and community outreach. • - Liaison Role: Act as a liaison between our Sponsor and CRO partners, internal teams, and clients to ensure smooth communication and coordination. • - Feasibility and Metrics Submission • - PSV Scheduling: Schedule Pre-Study Visits (PSVs) and ensure that all logistical and preparatory activities are completed. • - Positioning for Awards: Position our clients to maximize their probability of increased study awards by highlighting their unique capabilities and positive attributes. • - Competitive Edge Maintenance: Maintain a competitive edge for site selection by showcasing our clients' unique capabilities, particularly in diversity, community outreach, and other strengths that make them ideal candidates for trials. • - Documentation: Document all relevant study communications in a secure, centralized system weekly. • - Summary Compilation: Compile detailed study summaries highlighting key aspects and potential challenges. • - Information Transfer: Securely transfer information to the Clinical Data Integration team via our CRM for further processing. • - Team Collaboration: Collaborate with the Clinical Data Integration and Client Success teams to optimize site representation in project-managed studies. • - Record Keeping: Ensure all Salesforce records are up-to-date and that standardized processes are followed • - Network Growth: Continuously work towards maintaining a consistent flow of new and relevant study opportunities for our network.

🎯 Anforderungen

• Qualifications: • - Proven experience in clinical trial management, particularly in identifying and securing trial opportunities. • - Strong understanding of clinical research operations requirements. • - Communication and Sales Skills: Excellent communication, negotiation, sales, and customer service skills, with the ability to engage effectively with sponsors, CROs, and internal teams. • - Proficiency in using CRM systems and handling secure data management practices. • - Detail-oriented with strong organizational and documentation skills. • - Ability to work independently and as part of a team, managing multiple priorities effectively. • - Proactive and timely follow-up skills; the ability to organize applicable department timelines and follow up with internal and external stakeholder needs as needed. • - Self-motivated; able to work independently to complete tasks, respond to department requests, and collaborate with others to utilize their resources and knowledge to identify quality solutions. • - Flexible in nature to accommodate new program growth and change. • - Demonstrated track record of increasing revenue through the generation of leads. • Education/ Experience: • - Bachelor’s degree in Life Sciences, Business, Marketing, or related field. • - Minimum of 3-5 years of experience in clinical research or a related role within the pharmaceutical, biotech, or CRO industries.

🏖️ Vorteile

• What We Offer: • - A dynamic work environment with a focus on growth and professional development. • - Competitive salary and benefits package. • - Opportunities to significantly impact the success and expansion of our clinical trial network.