
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.
🕒 il y a 8 jours
🌲 North Carolina – Distant
💵 $86 000 - $170 000 / an
⏰ Temps Plein
🟡 Intermédiaire
🟠 Senior
👔 Manager
🦅 Parrain de Visa H1B
👻 Score fantôme 0%
🗣️🇺🇸🇬🇧 Anglais requis
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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.
• Serve as the primary point of communication and accountability for study start-up and maintenance activities on assigned projects • Oversee project activities of functional groups involved in site activation to ensure critical path activities are completed on-time and within budget • Ensure accurate compilation, management, tracking, and analysis of site activation activities in a timely manner • Support feasibility and/or site identification activities as needed • Work closely with assigned team members to expedite the Site Qualification and Selection process • Communicate Site Activation & Regulatory project status to the Sponsor, GPL/CPM, and project team • Partner with Commercial and Therapeutic Area Leadership to translate business priorities into integrated marketing initiatives
• A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related science OR two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and experience within clinical research (e.g. CRA, Reg Affairs) • Minimum of 4 years CRO/pharmaceutical industry experience, preferably in Start-up Management, Project Management, and/or Site Management experience • Proficient in cross-cultural communication • Proficient in both spoken and written English • Strong leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing • Ability to exercise sound judgment and make decisions independently and proactively identify and solve problems • Ability to provide experience and input into initiatives relating to interacting with sites and/or customers • Ability to motivate, lead and engage a team • Strong interpersonal skills in a fast-paced, deadline-oriented, and changing environment • Strong oral and written communication skills to clearly and concisely present information
• Competitive benefits package depending on location • Transparent compensation and pay equity • Inclusive and equitable workplace
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