Job Responsibilities This role will support late phase Hematology and Immunology portfolios. The PM II provides support to the Clinical Trial Manager/operational team in execution of the trial(s). These responsibility will include direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. 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 experienceGlobal 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-outStrong communication skills and the ability to work effectively in a fast-paced environment.Key Desired Behaviors & Skills Proactive, takes ownership, and works effectively with minimal directionStrong communication and collaboration skills with internal teams, sites, and vendorsStrong prioritization and organizational skills in fast-moving, complex environmentsWhy 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 building an inclusive culture - where you can authentically be yourself.



Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.We are continuously building the company we all want to work for and our customers want to work with. Why? 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.Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.Http://www.Syneoshealth.ComAdditional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when a#J-18808-Ljbffr

📌 Single Sponsor Clinical Project Manager Ii (Global Experience Needed) Fully Home Based In Spain, Bul (Madrid)
🏢 Syneos Health
📍 Madrid