Site Start Up Project Delivery - Home based any country LATAM
Syneos Health
ARG, Latin America , Argentina
hace 1 día


SSU Project Delivery - Home based any country LATAM

Focus in global projects not line management role

Argentina-Chile-Costa Rica-Brazil-Guatemala-Colombia-Peru-Mexico

Come discover what our 25,000+ employees already know : work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.

As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason we improve patients’ lives around the world.

Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.

Why Syneos Health

  • SyneosHealthLife means we’re committed to our Total Self culture where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.
  • We believe our success is a direct result of the people who are driving it you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you.
  • That’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.

  • 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 responsibilities

  • Collaborates with major functional area leads (SSU Country Managers, Project Management, and Clinical Management) to identify and evaluate 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 assessments.

  • Develops and maintains strategic relationships with customers in alignment with their assigned projects. May collaborate with business leads for business development, alliance management, contracts and proposals development, project management, and clinical management to achieve project goals.
  • Ensures that individual project targets and client needs are met, services are provided with the highest quality standards, and policies and procedures are followed.

    Contributes to change initiatives across and within the SSU department.

  • Provides oversight of all project SSU deliverables which encompasses all activities from site selection through site activation ready.
  • Assumes accountability on SSU deliverables including, but not limited to :
  • Start-up regulatory activities (submissions, oversight of communication to competent authorities / ethics committees, import / export licenses, study maintenance submissions);
  • Oversight of delivery of executed clinical trial agreements and investigator budgets with investigator sites
  • Establishing Essential document collection leading to site activation;
  • Overall SSU timelines to site activation.
  • Develops plans in accordance with Standard Operating Procedures and / or sponsor-scoped process. Complies with all controlled document requirements and other requirements to ensure quality deliverables.
  • Develops and manages integrated site start-up timelines and reports weekly progress including plans to address potential timing risks / gaps.
  • Work with the project leadership to define the strategy to execute against milestones and key deliverables. Prepares and presents overall SSU strategy and status at client meetings and communicates outcomes to project team
  • Monitor team efficiency and adherence to project timelines. Ensure quality of designated deliverables. Responsible for driving team efficiencies with a goal of reducing waste and increasing SSU predictability.
  • Develop, maintain and publish project KPI’s that track project quality, delivery and predictability
  • Provides oversight of the scope of work, budget and resources. Reviews the project SSU budget with the functional leads, project PM, and the SSU Business Unit Controller against project milestones and budget to ensure project profitability.
  • Takes corrective measures where necessary to keep project in line with budget and gross profit expectations.

  • Uses professionally recognized tools for planning and management of scope, timeline, resources, and ensures that minimum hours are used for tasks.
  • If out-of-scope work is requested, notifies the project PM and her / his SSU manager and track out of scope until assigned to back log.

  • Prepares the core submission documents and core clinical trial application dossier.
  • Assists in development of Patient Information Sheet (PIS) / Informed Consent Form (ICF) in collaboration with the PM and medical department.
  • Oversees collation, quality review and submission of country-specific applications.
  • Accountable for the timely follow-up for Ethics Committee / Competent Authority enquiries or objections in collaboration with the country SSU Specialists.
  • Meets or exceeds the planned submission / approval timelines; if forecasted timelines are not reached or if any potential issue is identified, solves or escalates the problem quickly.

    In parallel with project deliverables, identifies best practices and initiates / participates in process improvement initiatives in conjunction with the global SSU leadership plan.

  • Accountable for the negotiation and execution of clinical trial agreements and budgets in accordance with agreed timelines.
  • Includes coordination of internal and external stakeholders in the development and / or provision of required clinical trial agreement templates and investigator site budgets, oversight of local contract negotiator colleagues and assistance in resolving negotiation barriers, and periodic progress reporting to the client and other stakeholder groups.

    May include providing assistance and guidance to SSU Lead colleagues in their coordination of clinical trial agreement activities.

  • Develops new business opportunities whenever possible (e.g., while in attendance at professional conferences / seminars), participates in new business development activities including participation at client presentations.
  • Reviews proposals, attends client sales-focused meetings, and provides information to support business development activities.

  • Actively participate in team meetings. Designs presentations and delivers information in a way that allows the audience to understand the information and interact appropriately.
  • Designs and delivers basic training courses.

  • May be recognized as a subject matter expert in specific regulatory areas (pediatric studies, advanced therapy products, medical devices, etc.
  • and / or in development and review of Standard Operating Procedures (SOPs) and Work Instructions (WI) to support new or existing processes.

    Reportar esta oferta

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Mi Correo Electrónico
    Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
    Formulario de postulación