Remote Clinical Delivery Program Lead

Parexel International; México; A distancia; MXN 2.185.000 - 3.824.000; Jornada completa

Descripción de la vacante

Parexel International is seeking a Program Lead, Clinical Delivery to lead exploratory and biopharmaceutics clinical development plans at the molecule level. You will oversee design through execution, including vendor management, timelines, risks, and budget, guiding the global clinical team toward on-schedule, on-budget outcomes.

The role requires strong leadership, cross-cultural collaboration, and experience managing complex trials and regulatory documents within a virtual, international

Formación

• Bachelor’s degree in a science related field from an accredited college or university.
• 3-years’ experience in the pharmaceutical industry with direct experience of managing clinical studies, ideally in exploratory and biopharmaceutics clinical development (5+ year preferred).
• Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials.
• Ability to influence and oversee TPOs to enable delivery of trial level deliverables.
• Demonstrated knowledge and experience with project management tools and processes.
• Demonstrated ability to work effectively cross‑culturally and in a virtual work environment.
• Demonstrated ability to influence both internal and external environments appropriately and forge strong working relationships.
• Demonstrated problem‑solving skills; able to anticipate and recognize systemic problems, diagnose root causes, and take corrective actions to prevent recurrence within the team.
• Strong self‑management, organizational and interpersonal skills, and the ability to be flexible in varying environments and with multiple customer groups.
• Strong leadership and networking skills.
• Excellent oral and written communication skills; able to communicate clearly and with team members and leadership
• Strong computer skills; skilled at using Word, Excel, PowerPoint, and Microsoft Project
• Ability to travel (up to 10% expected)

Responsabilidades

• Leads and has expertise in the implementation and integration of clinical project management processes and tools.
• Works with Third Party Organizations (TPOs) to execute the defined clinical strategy, overseeing key trial deliverables.
• Develops and maintains up-to-date clinical plan timelines and process maps (if appropriate) ensuring communication of progress to the broader molecule team.
• Partners with the financial organization, cross-functional partners, and geographies, to develop and manage the overall clinical budget for the molecule level book of work including initiation and management of the change process.
• Proactively identifies and communicates clinical risk assessment and mitigation/contingency plans within team and to functions, affiliates, and leadership.
• Accountable and responsible for oversight of clinical trial operations and delivery of clinical project milestones on time, on budget
• Create and manage implementation timeline and clinical trial activities
• Involved in selection process and management of vendors, ensuring day to day oversight for operational deliverables of external network of vendors to ensure on time and on budget clinical project deliverables
• Serves as the point of contact for the global clinical team, to resolve clinical implementation issues (internal and external), lead risk assessments and contingency planning, and effective communication across and upward
• Partner with regulatory and medical to ensure safety management and monitoring processes are implemented

Conocimientos

Leadership

Project management

Communication

Vendor management

Educación

Bachelor’s degree in science

Advanced scientific degree

Descripción del empleo

Parexel International is seeking a Program Lead, Clinical Delivery to lead exploratory and biopharmaceutics clinical development plans at the molecule level. You will oversee design through execution, including vendor management, timelines, risks, and budget, guiding the global clinical team toward on-schedule, on-budget outcomes.

The role requires strong leadership, cross-cultural collaboration, and experience managing complex trials and regulatory documents within a virtual, international