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Clinical Trial Manager II - Study Manager; RWE, negotiation

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: Syneos Health, Inc.
Contract position
Listed on 2026-02-06
Job specializations:
  • Management
    Healthcare Management
Job Description & How to Apply Below
Position: Clinical Trial Manager II - Study Manager (RWE, contract negotiation)
Location: Greater London

Overview

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

Updated: February 3, 2026
Location: London, LND, United Kingdom
Job : -OTHLOC-3526-2DR

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Role Responsibilities
  • Lead operational delivery of multiple Real World Evidence (RWE) and clinical studies (typically 10–12 studies), ensuring high‑quality and timely execution across global regions.
  • Apply global operational expertise to support feasibility, site engagement, and study startup activities.
  • Utilize prior CRA experience (asset) to guide monitoring strategy, assess site performance, and identify operational risks early.
  • Act as a key facilitator for external research collaborations, serving as the primary contact for vendor and partner engagement.
  • Manage contract processes by collecting operational requirements, identifying red flags, understanding stakeholder needs, and ensuring smooth contract negotiation and execution.
  • Lead budget development and oversight, including FMV analysis, cost metrics, and milestone creation, ensuring accurate forecasting and proactive financial management.
  • Oversee vendor performance and relationship management, ensuring alignment on deliverables, timelines, data flow, and study quality.
  • Maintain oversight of operational risks and mitigation strategies across all assigned studies, escalating issues as needed.
  • Collaborate effectively within cross‑functional teams (clinical, data management, regulatory, medical, procurement, etc.) to ensure operational alignment and problem resolution.
  • Apply strong project management skills to prioritize workload, manage timelines, track progress, and ensure adherence to study plans.
  • Utilize strategic thinking and analytical skills to interpret study data, anticipate challenges, and drive continuous improvement in study processes.
  • Communicate proactively and clearly with internal stakeholders, external partners, and study teams, ensuring transparency and alignment on expectations and timelines.
  • Contribute to inspection readiness and quality compliance across studies, supporting audits and regulatory activities as required.
Qualifications
  • Experience in Real‑World Evidence (RWE) preferred.
  • Background in clinical trial or study management with solid knowledge of GCP, monitoring, and clinical/regulatory operations.
  • BS/Nursing with 2+ years of relevant experience, or MS/PhD with 1+ year.
  • Proven experience overseeing CROs, external partners, and vendors
    .
  • Strong contract negotiation and contract facilitation experience (gathering requirements, identifying red flags, supporting negotiation flow).
  • Skilled…
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