Clinical Project Manager – Regional/Global, Mexico & Argentina

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Oversee interdisciplinary clinical research programs in the role of Project Manager.

• Ensure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and regulatory guidelines.

• Serve as the main point of contact between the Company and the Customer throughout the project lifecycle, including launch, execution, and closure.

• Guide clinical teams to maintain quality standards, adhere to timelines, and manage budgets effectively.

• Supervise the financial outcomes and deliverables of assigned projects and/or project regions.

• Collaborate with project conduct partners and proactively identify and resolve issues.

• Keep project information updated in relevant databases and systems.

• Monitor and assess project progress using timelines and tracking/analysis tools.

• Handle project components related to inspection readiness, including Trial Master Files.

• Oversee the creation and execution of project plans.

• Prepare, coordinate, and deliver project presentations at both internal and external meetings.

• Lead and mentor Project Support staff, project management team members, and clinical personnel.

• Compile project management reports for clients and internal stakeholders.

• Develop and implement resource strategies, contingency plans, and risk mitigation approaches.

• Engage in bid defense meetings.

• Cultivate relationships with current clients to generate new or additional business opportunities.

• Stay informed about therapeutic landscapes and trends in drug development.

• Educate and support new Project Managers and facilitate training for teams.

• Provide direct management to project management team members and clinical monitoring staff as necessary.

⛳️ Requirements

• Proven experience as a Clinical Project Manager leading interdisciplinary clinical research programs.

• Familiarity with Good Clinical Practices (GCPs).

• Understanding of relevant Standard Operating Procedures (SOPs).

• Knowledge of regulatory standards.

• Capability to manage project quality, timelines, and budgets effectively.

• Ability to oversee project financial performance.

• Skill in managing project deliverables and project regions.

• Proficiency in coordinating project conduct partners and addressing issues.

• Experience in maintaining project information in databases and systems.

• Competence in managing timelines and utilizing tracking/analysis tools.

• Experience with inspection readiness and Trial Master Files.

• Proven track record in developing and implementing project plans aligned with Controlled Documents.

• Ability to prepare, coordinate, and present project materials for both internal and external audiences.

• Experience in directing and mentoring project management and clinical teams.

• Skilled in preparing project management reports.

• Experience with resource strategy implementation.

• Background in contingency planning and risk mitigation strategies.

• Participation in bid defense meetings is required.

• Ability to foster client relationships and drive business growth.

• Awareness of therapeutic environments and trends in drug development.

• Capability to train and support Project Managers and clinical staff.

• Equivalent experience, skills, and/or education will also be taken into account.

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged management team.

• Access to technical and therapeutic training.

• Recognition from peers.

• Comprehensive total rewards program.

• A culture that emphasizes total self.

• Initiatives promoting diversity, inclusion, and a sense of belonging.