(Uwc068) - Sponsor Dedicated Project Manager Ii (Clinical Trial Leader) Fully Remote In Uk Or Spain.

Project Manager IISyneos 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.We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.Why Syneos HealthWe are passionate about developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition; and a 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.Job ResponsibilitiesManage a project as a project manager overseeing interdisciplinary clinical research studies and ensure compliance with GCP, relevant SOPs, and regulatory requirements.Act as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer's and the Company's contractual agreement.Lead project team to ensure quality, timelines, and budget management.Accountable for the financial performance of each project.Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.Ensure studies are conducted in compliance with GCP, relevant SOPs, and regulatory requirements.Accountable for all project deliverables for each project assigned.Responsible for quality and completeness of TMF for assigned projects.Accountable for maintenance of study information on a variety of databases and systems.Responsible for study management components of inspection readiness for all aspects of the study conduct.Oversight for development and implementation of project plans.Plan, coordinate, and present at internal and external meetings.Prepare project management reports for clients and management.Develop contingency planning and risk mitigation strategies to ensure successful delivery of study goals.#J-18808-Ljbffr