Director Clinical Project Management

CTI Clinical Trial and Consulting Services

Madrid

Presencial

EUR 80.000 - 110.000

Jornada completa

Hace 7 días
Sé de los primeros/as/es en solicitar esta vacante

Recibe más respuestas de empleadores

Envía un currículum específico para el puesto de trabajo en cuestión de minutos.

Descripción de la vacante

CTI Clinical Trial and Consulting Services in Madrid seeks a seasoned Clinical Project Leader to oversee the end-to-end execution of multiple trials. You will ensure compliance with ICH, GCP, and regulatory standards while coordinating cross-functional teams across global sites.

You will mentor CPMs and CPCs, manage budgets and timelines, and communicate with sponsors and executives to mitigate risks and deliver high-quality results for patients and caregivers, advancing medicines that improve

Formación

  • Bachelor’s degree in allied health fields (nursing, pharmacy or health science) or equivalent.
  • 12 years of clinical research or CTI project management experience.
  • Experience managing clinical trials across global operations.
  • Fluent in English.

Responsabilidades

  • Plan, implement, and evaluate the full execution of assigned clinical trials.
  • Oversee multiple trials from planning to analysis for client delivery.
  • Coordinate CPMs and CPCs across functions and with the client.
  • Ensure compliance with ICH, GCP, and regulatory guidelines.
  • Provide leadership and mentoring to CPMs and CPCs.
  • Oversee project budgets, timelines, and resource planning.

Conocimientos

Fluent English
Clinical trial management

Educación

Bachelor’s degree in allied health fields

Descripción del empleo

What You’ll Do
  • Plan, implement, facilitate and evaluate the full execution of assigned clinical trials; oversee management of multiple clinical trials from the planning phase to the analysis phase for delivery to client;
  • May function in global lead role on assigned trials and participate in day to day operations and/or oversight of trial activities and deliverables
  • Ensure the operational aspects of the functional areas comply with International Council for Harmonization (ICH) guidelines, Good Clinical Practices (GCP), applicable regulatory guidelines and trial procedures
  • Ensure that assigned Clinical Project Managers (CPM) and/or Clinical Project Coordinators (CPC) coordinate the organization and implementation of a clinical trial and manages the activities between all functional areas and the client
  • Serve as primary senior interface on the project with executive management at CTI and the sponsor; provide effective client management to prevent and mitigate trial issues; elevate identified trial, CPM or CTI issues to executive management as needed; actively participate in resolution activities
  • Oversee preparation of all study plans and project timelines and monitor against project progress; ensure project activity compliance with Plan(s); suggest and implement alternative solutions to problems with study timelines, schedules, resources, budgets, etc. Take corrective action where necessary
  • Assess resource needs within team, with other CPM directors, Executive Director and other functional area managers to establish appropriate project team; monitor ongoing resource needs for project
  • Ensure that appropriate project management tools are used to track and report project progress and metrics; ensure timely entry of project information by all team members throughout the life of the project
  • Ensure training of assigned project teams; participate in staff training for his/her projects or other projects, dependent upon expertise
  • Oversee the management of budgeted hours by the CPM, who evaluates and manages regional project budget against project milestones; ensure that the CPM takes corrective measures where necessary to keep project in line with budget expectations
  • Ensure that the CPM assesses scope of work against client contractual agreements and assist in changes of scope orders; provide review of changes in scope notifications and work with Business Operations to ensure completion of needed contract amendments
  • Synthesize and analyze new information against past experience, project information related to trial milestones in contracts and the sponsor expectations to develop strategies to facilitate effective problem solving and advancement of the project; keep CTI executive management and the client informed; ensure that the CPM initiates corrective action
  • Conduct or attend trial team and sponsor meetings; ensure that agendas and minutes are effectively prepared to facilitate trial communication and documentation of trial oversight, discussions and decisions
  • Review weekly and/or monthly project status reports as needed prior to forwarding to client to ensure the quality of those reports, as well as all other sponsor deliverables
  • Report project progress, issues and scope of work considerations to executive management
  • Provide input for new business development (NBD) proposals, assist in project budget preparation / review and represent project management services during NBD client presentations; participate in new business recruitment and marketing activities; seek NBD opportunities when appropriate and communicate these opportunities to Business Development
  • Provide supervision, guidance and mentoring to CPMs while encouraging independence and refinement of the CPM’s skills; provide regular performance evaluation and feedback to direct reports
  • Review and assess internal and external quality assurance reports for assigned projects and ensure corrective action as necessary by the project management team
  • Provide leadership in process improvement activities and initiatives; participate in the development and enhancement of integral aspects of the CPM operations
  • Provide leadership and share expertise with clinical operations staff; facilitate the development of reference and resource materials for CPMs and clinical operations; participate in staff training and development activities
  • Coach and train others in the CPM practices; promote and actively participate in the professional development of all CPM and CPC staff
  • Participate in business development opportunities and the enhancement of globalization processes
What You’ll Bring
  • Bachelor’s degree in allied health fields such as nursing, pharmacy or health science, preferably with clinical trial management experience or an equivalent combination of education and relevant work experience
  • 12 years of clinical research experience and/or experience in CTI clinical project management demonstrating a clear and thorough understanding of global trial management processes and the operation of all clinical trial functional areas
  • Experience in management of clinical trials
  • Fluent in English
About CTI

We invest in your professional growth. Our structured mentoring program, leadership development courses, and dedicated training department provide the support you need to excel. We also encourage ongoing education to help you achieve your professional goals.

  • Join an Award-Winning Team – Join a global team spanning 60 countries, recognized for its award-winning culture that prioritizes people. We support your work-life balance with hybrid work opportunities. Through our CTI Cares program, you’ll have opportunities to give back to your community and the world.
  • Make a Lasting Impact

At CTI, your work directly contributes to advancing medicine. You’ll play a vital role in developing life-changing treatments for patients with chronic and critical illnesses. Together, we move medicine forward, making a difference for those who need it most.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra y suelta tu archivo aquí
Similar jobs

Puestos de trabajo similares que vale la pena comparar

Director Clinical Project Management
Director Clinical Project Management

CTI Clinical Trial and Consulting Services • España

Híbrido
EUR 90.000 - 120.000
Hybrid work opportunities
Mentoring program
Training & development
Clinical Project Manager III/ Senior CPM (level dependent on experience)
Clinical Project Manager III/ Senior CPM (level dependent on experience)

CTI Clinical Trial and Consulting Services • España

Híbrido
EUR 65.000 - 90.000
Hybrid work opportunities
Mentoring and career development
Project Manager, Laboratory Services
Project Manager, Laboratory Services

Consulting, Inc. • País Vasco

Híbrido
EUR 70.000 - 110.000
Hybrid work opportunities
Global team environment
Professional development
Clinical Project Assistant/ Coordinator
Clinical Project Assistant/ Coordinator

CTI Clinical Trial and Consulting Services • Madrid

Presencial
EUR 30.000 - 45.000
Clinical Trial Manager - IQVIA Biotech
Clinical Trial Manager - IQVIA Biotech

IQVIA • Madrid

Presencial
EUR 60.000 - 90.000
Project Manager
Project Manager

Worldwide Clinical Trials • Madrid

Presencial
EUR 50.000 - 75.000
Clinical Project Manager
Clinical Project Manager

Precisionmedicinegroup • España

Presencial
EUR 60.000 - 90.000
Global Clinical Program Director
Global Clinical Program Director

CTI Clinical Trial and Consulting Services • España

Híbrido
EUR 90.000 - 120.000
Hybrid work opportunities
Mentoring program
Training & development
Global Senior Trial Delivery Manager - Sponsor Dedicated
Global Senior Trial Delivery Manager - Sponsor Dedicated

IQVIA • Madrid

Presencial
EUR 60.000 - 85.000
Global Clinical Trial Project Lead
Global Clinical Trial Project Lead

CTI Clinical Trial and Consulting Services • España

Híbrido
EUR 65.000 - 90.000
Hybrid work opportunities
Mentoring and career development