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Clinical Trial Manager - Sponsor Dedicated

IQVIA Holdings Inc.

São Paulo, Brazil

*Please upload your CV in English or Spanish when applying!

Job Summary
Clinical Trial Manager is an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. This professional will be an essential member of the core project team leading the team and responsible for project deliveryof clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.

-> Focusing on project delivery, productivity and quality to result in strong financial performance and customer satisfaction, this professional will run their own studies dedicated to one specific sponsor.

-> Leverage therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.

What will you do?

  • Prepare, Participate and lead bid defenses in partnership with Business Development for regional studies.
  • Understand project strategy and operationalize the agreed upon approach.
  • Accountable for the strategic planning and execution of clinical studies as per the contract while optimizing speed, quality and cost of delivery.
  • Ensure consistent use of study tools, training materials and compliance with standard processes, policies and procedures.
  • Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
  • Collaborate with other functional groups within the company when necessary to support milestone achievement and to manage study issues and obstacles.
  • Monitor progress against contract and prepare/present project information proactively to internal and external stakeholders.
  • Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
  • Achieve project quality by identifying quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.
  • Serve as primary project contact with customer and own relationship with the project’s key customer contact(s).
  • Communicate/collaborate with IQVIA business development representatives as necessary.
  • Build the cross-functional project team and lead their efforts, responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.
  • Ensure the financial success of the project.
  • Forecast and identify opportunities to accelerate activities to bring revenue forward.
  • Identify changes in scope and manage change control process, as necessary.
  • Identify and communicate lessons learned and best practices to promote continuous improvement.
  • Adopt corporate initiatives and changes and serve as a change advocate when necessary.
  • Provide input to line managers of their project team members’ performance relative to project tasks. Support staff development.
  • Mentor less experienced project team members on assigned projects to support their professional development.

What do we expect from you?

  • Bachelor's Degree in Life sciences or related field.
  • Greater than 7 years clinical research experience including 4 years project management experience or equivalent combination of education, training and experience.
  • Knowledge of clinical trial conduct, and skill in applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
  • Broad protocol knowledge, therapeutic knowledge desired.
  • Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.
  • Strong written and verbal communication skills including good command of English and Spanish language.
  • Strong negotiation and customer management skills.
  • Strong problem solving skills.
  • Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.
  • Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.;
  • Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
  • Ability to handle conflicting priorities and to work strategically to realize project goals, identifying and developing positive and compelling visions for the successful delivery of the project.
  • Results-oriented approach to work delivery and output. Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
  • Ability to work across geographies displaying high awareness and understanding of cultural differences.
  • Good understanding of project financials including experience managing, contractual obligations and implications.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

Job posted: 1970-01-01

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