Clinical Project Manager - IQVIA Biotech - Oncology

IQVIA; Fatih; Presencial; TRY 600.000 - 900.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Project Lead to drive clinical study delivery, leveraging therapeutic expertise and IQVIA’s solutions. The role focuses on delivering studies on time, within scope and budget while maintaining quality and regulatory compliance.

You will work with core project teams, collaborate across functions, and act as a primary contact with key customers. The position offers opportunities for leadership and professional development within IQVIA's global clinical research services.

Formación

• Bachelor's degree and related field required.
• 5 years of prior relevant experience including >1 years project management experience.
• Advanced knowledge of the job area and broad knowledge of related areas.
• Knowledge of clinical trials and regulatory requirements (ICH GCP)

Responsabilidades

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
• Deliver and manage smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Execute clinical studies per contract while optimizing speed, quality and cost.
• Set objectives of the core project team and assess performance.
• Collaborate with other functional groups to support milestone achievement and issue management.
• Monitor progress against contract and present project information to stakeholders.
• Manage risks and contingencies and lead problem solving.
• Ensure project quality by addressing risks and implementing CAPA.
• May serve as primary/backup project contact with customer and manage relationships.
• Build cross-functional project team and oversee collaboration for delivery.
• Ensure financial success of the project and forecast opportunities.
• Identify scope changes and manage change control.
• Capture lessons learned and implement best practices.
• May be primary vendor contact and lead vendor management.
• Adopt corporate initiatives and act as change advocate.
• Provide input to line managers on team performance.
• Mentor less experienced team members for professional development.

Conocimientos

Project management

Clinical trial knowledge

Educación

Bachelor's Degree Life sciences or related field

Descripción del empleo

Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.

Essential Functions

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
• May be responsible for delivery and management of smaller, less complex, regional studies.
• Develop integrated study management plans with the core project team.
• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.
• 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 and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as 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 lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;
• 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 and mentor less experienced project team members on assigned projects to support their professional development.;

Qualifications

• Bachelor's Degree Life sciences or related field
• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience.
• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.