12 ene
Syneos Health
Xico
.Sr Site Activation Manager sponsor dedicated Home Based MexicoUpdated: November 28, 2024Location: Mexico-Latin America - MEX-Home-BasedJob ID:24006035Sr Site Activation Manager sponsor dedicated Home Based Mexico (VISA required)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.Job responsibilitiesCollaborates with major functional areas including, but not limited to: Business Development, Alliance Management, Contracts and Proposals Development, SSU Country Managers, Project Management, Clinical, Data Management and Medical Writing.Identifies and evaluates fundamental issues pertaining to Site Start-Up, project regulatory pathway, successful patient enrollment, interpret data on complex issues, make good business decisions, and ensure solutions are implemented.Ensures all project deliverables meet the internal and customers' expectations as per contracted deliverables, providing accurate projections, reports and updates, and ongoing risk identification,
mitigation and management.Develops and maintains relationships with customers in alignment with their assigned projects.Ensures that individual project targets and client needs are met, services are provided with the highest quality standards, and policies and procedures are followed.Provides oversight of all project start-up deliverables which encompasses all activities from site selection through site activation ready and into the life cycle maintenance of projects.Assumes accountability on start-up deliverables including, but not limited to:Site Identification and selectionStart-up and life cycle maintenance regulatory activities (submissions, oversight of communication to competent authorities/ethics committees, import/export licenses and extensions, study maintenance and amendment submissions)Oversight of delivery of executed clinical trial agreements and investigator budgets with investigator sites,
including any required amendmentsEstablishing and overseeing Essential Document collection leading to site activationOverall SSU timelines, prior to and following site activation.
Including any realignment required due to amendment needs.Develops plans in accordance with Standard Operating Procedures and/or sponsor-scoped processes
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