Clinical Trial Manager II - Study Manager (RWE, contract negotiation)

Syneos Health

Industria de Investigación Farmacéutica

Barcelona, Cataluña - Spanien

Manager / Gestor de equipos

Experteer Overview

In this role you will lead the operational delivery of Real World Evidence and clinical studies, ensuring quality and timely execution across global sites. You collaborate across cross‑functional teams to align study plans with business goals and regulatory expectations. You will drive contract negotiation, vendor management, and budget oversight, shaping study strategies and risk mitigation. The position offers impact on RWE programs and external collaborations in a fast‑paced, mission‑driven environment. This is a chance to influence study outcomes and help accelerate therapy delivery.

Compensaciones / Beneficios

Total Self culture
career development and progression
supportive and engaged management
total rewards program

Responsabilidades

Lead the operational delivery of multiple RWE/clinical studies (10–12) across global regions
Support feasibility, site engagement, and study startup activities
Guide monitoring strategy using prior CRA experience and assess operational risks early
Serve as primary liaison for external research collaborations and vendor engagement
Manage contract processes including requirements gathering, red flags, and negotiation
Lead budget development and oversight with FMV analysis, cost metrics, and milestones
Oversee vendor performance and relationship management for deliverables and data flow
Maintain oversight of operational risks with escalation when needed
Collaborate with cross‑functional teams to ensure alignment and issue resolution
Apply project management to prioritize workload, timelines, and study plans
Use strategic thinking to interpret data, anticipate challenges, and improve processes
Communicate proactively with stakeholders and study teams for transparency
Contribute to inspection readiness and regulatory activities as required

Requisitos principales

Experience in Real‑World Evidence (RWE) preferred
Background in clinical trial or study management with knowledge of GCP and regulatory operations
BS/Nursing with 2+ years or MS/PhD with 1+ year
Proven experience overseeing CROs, partners, and vendors
Strong contract negotiation and facilitation experience
Skilled in budget management, FMV assessment, and milestone planning
Ability to interpret study‑level data and identify operational risks
Understanding of protocol feasibility and operational challenges
Excellent communication and cross‑cultural skills; English fluency
Highly organized, detail‑oriented, proficient with spreadsheets and data systems
Strong analytical, problem‑solving, and cross‑functional collaboration skills

Excellent communication Cross‑cultural awareness Cross‑functional collaboration GCP knowledge Budget management / FMV analysis Milestone planning

Descripción del puesto

In this role you will lead the operational delivery of Real World Evidence and clinical studies, ensuring quality and timely execution acros…

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