Biometrics and PV Business Support Manager

🕒 il y a 5 jours

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

👔 Manager

🇬🇧 Parrain de Visa de Travailleur Qualifié UK

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👻 Score fantôme 10%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 employés

🏥 Santé

💼 Conseil

📦 Logistique

Healthcare • Consulting • Logistics

Worldwide Clinical Trials est une organisation mondiale de recherche contractuelle (CRO) qui offre des services complets d'essais cliniques. Ils se spécialisent dans le soutien aux études dans divers domaines thérapeutiques tels que l'oncologie, la cardiologie et les maladies rares. Avec plus de 30 ans d'expérience, Worldwide Clinical Trials met l'accent sur un soutien personnalisé et des solutions sur mesure tout au long du cycle de développement des médicaments. Leurs services incluent la surveillance clinique, la gestion des données, le recrutement de patients et le conseil réglementaire, garantissant précision et attention sur-mesure pour chaque essai clinique.

Description

• Oversee, coordinate, maintain, and track all Business Development activities within the Biometrics and Pharmacovigilance department • Oversee, coordinate, monitor, and track all active bids, proposals, and departmental change orders • Triage proposals and budgets based on SME input requirements and develop triage criteria with SMEs • Develop budgets and proposal text according to agreed standards when SME input is not required • Develop draft budgets and proposal text for SME review when input is required • Respond to RFPs and RFIs and develop bids, proposals, statements of work, presentations, and supporting materials • Work with Account Directors, operational teams, and third-party vendors to integrate solutions into complete proposals and statements of work • Identify proposal trends that may require changes to departmental strategy • Proofread, edit, rewrite, and revise documents for readability and consistency • Establish priorities and target dates to meet proposal deadlines • Gather information and customize content with subject matter experts • Respond to routine and non-routine enquiries and obtain assistance for complex enquiries • Provide budget tool and proposal training and mentoring for Biometrics and PV colleagues • Maintain standard proposal and bid defense slides • Maintain the departmental RFI Library • Perform other duties assigned by the supervisor

🎯 Exigences

• Sound understanding of Biometrics and Pharmacovigilance operations • Strong planning, managing, monitoring, scheduling, and critiquing skills • Excellent written and verbal communication skills • Strong interpersonal skills for working in a dynamic, fast-paced, deadline-oriented team • Ability to handle multiple short-term assignments and project deliverables with strict deadlines • Ability to exercise sound judgment and make decisions independently • Excellent self-motivation skills • Proficiency in all MS-Office applications, including Microsoft Word • High level of Excel proficiency • Ability to train other personnel • Minimum 5 years’ experience in CRO operations involving Data Management, Biostatistics, or Pharmacovigilance • Bachelor’s Degree required; preference for Life Sciences, Communications, Journalism, or Marketing • Experience drafting bids and proposals in a CRO environment, or in pharma/biotech outsourcing preferred • Knowledge of the CRO/Pharmaceutical industry • Knowledge of sales support activities • Strong understanding of study design, project management, and operational requirements for successful study implementation • Ability to advise and interact with all levels of management • Excellent analytical and mathematical skills

🏖️ Avantages

• Equal employment opportunities • Diverse and inclusive work environment • Collaboration and creativity-focused culture • Supportive teams and accessible leaders • Employee opportunities to succeed and thrive

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