Description Single Sponsor Clinical Project Manager II (Integral experience needed) Fully home based in Spain, Bulgaria, Poland or UK.Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.

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; Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. The PM II provides support to the Clinical Trial Manager/operational team in execution of the trial(s). The Lead maintains effective communication with the project team through oral and written correspondence and status reports to ensure alignment with study timelines.

Other tasks will include reviewing, developing, and writing clinical trial documents and manuals, including study manuals, laboratory or biomarker plans, and other supporting documents, plus the creation of the Master ICF template and review/approve site changes (in consultation with legal, safety when warranted), plus update template for new risks and new amendments information.

Essential

Requirements• Prior sponsor-side experience• Global study experience, rather than experience limited to a single region.

- Oncology, Hematology, or Immunology therapeutic area expertise,



ideally with experience supporting complex or pivotal studies.Important Experience• End-to-end study management experience, from study start-up through close-out• Strong communication skills and the ability to work effectively in a fast-paced environment.Learn more about Syneos Health.Further, nothing contained herein should be construed to create an employment contract. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.Summary Roles within Clinical Project Management job family are responsible for planning, directing, creating and communicating clinical study time-lines. Ensures consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets. Ensures studies are conducted within clinical trial protocols, monitoring progress and following up with team members and line managers when issues develop. The majority of time is spent overseeing their area of responsibility, planning, prioritizing, and/or directing the responsibilities of employees. Goal are achieved through management of process, policy, and performance of direct and/or indirect reports. Delivers operational results that have moderate impact on the immediate achievement of results for the team. Understands basic management approaches such as work scheduling, prioritizing, coaching and process execution.

📌 Single Sponsor Clinical Project Manager II (Global experience needed) Fully home based in Spain, Bul (Madrid)
🏢 Syneos Health
📍 Madrid