Syneos Health · CanadaPrepare for this interview
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CTM II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver - for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: 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 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. Job Responsibilities Develop, coordinate, and implement Phase 1 clinical research studies at the organization's facilities, ensuring adherence to study protocols and timelines Collaborate with the principal investigator to design study protocols and ensure scientific integrity Liaise between research subjects, client teams, investigators, and clinic operations teams to facilitate smooth communication and coordination Plan logistics and resource usage for clinical trials, including scheduling, staffing, and equipment needs Track study progress in alignment with project milestones, client deliverables, and budget, and provide regular updates to stakeholders Ensure compliance with applicable regulations globally and by region, including Good Clinical Practice (GCP) guidelines Supervise experienced support employees and/or entry-level individual contributors, planning, prioritizing, and directing their tasks to ensure efficient workflow and high-quality output Deliver operational results that have a moderate impact on the immediate achievement of results for the team, contributing to the overall success of the organization Adapt new procedures, techniques, and tools to improve clinical trial processes and outcomes Understand basic management approaches such as work scheduling, prioritizing, coaching, and process execution
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