Clinical Project Manager

more-jobs; Vevey; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Zusammenfassung

Proclinical, on behalf of its client, is seeking a Clinical Project Manager to lead a portfolio of early-phase clinical trials in Switzerland. You will oversee a small team, ensure GCP compliance, and drive quality and timely execution across study teams, sponsors, and CROs.

Responsibilities include planning, coordinating, and tracking milestones, promoting collaboration, and fostering development within the team while maintaining up-to-date training records and adherence to SOPs.

Qualifikationen

• Tertiary qualification in health, social or biological sciences.
• Experience in managing clinical studies, preferably early-phase.
• Knowledge of HREC, RGO, GCP guidelines and NHMRC guidelines.
• Proven leadership and team development in a CRO/clinical research setting.

Aufgaben

• Plan, coordinate and manage trials to meet sponsor and protocol timelines.
• Develop project plans, track milestones and ensure objectives are met.
• Ensure trial execution aligns with GCP, SOPs and regulatory requirements.
• Facilitate communication between sponsors, CROs and study teams.
• Define stakeholder responsibilities and key milestones clearly.
• Support continuous improvement of trial management processes and tools.
• Lead, motivate and develop the clinical trial team to high performance.
• Provide training and empower team members in their roles.
• Monitor team performance and coach to ensure successful outcomes.
• Ensure compliance with site policies and training requirements.

Kenntnisse

Leadership

Stakeholder mgmt

GCP knowledge

Team development

MS Office

Ausbildung

Health/bio science degree

Tools

MS Office

Jobbeschreibung

Ready to lead projects that bring life-changing treatments to the world? Join our client and assist in making a difference to clinical research.

Proclinical is seeking a Clinical Project Manager to oversee and deliver a portfolio of clinical trials with a focus on quality, compliance, and timely execution. In this role, you will lead a small team, ensuring adherence to protocol requirements, Good Clinical Practice (GCP), and standard operating procedures (SOPs). This position requires strong leadership, organizational, and communication skills to foster collaboration among stakeholders and drive successful trial outcomes.

Responsibilities

• Plan, coordinate, and manage clinical trials to meet sponsor and protocol requirements within agreed timelines.
• Develop project plans, track milestones, and ensure the achievement of project objectives.
• Ensure clinical trial execution aligns with applicable regulations, GCP guidelines, and internal SOPs.
• Facilitate effective communication and collaboration between sponsors, CROs, and study teams.
• Clearly define stakeholder responsibilities, study requirements, and key milestones.
• Support the continuous improvement of clinical trial management processes and tools.
• Lead, motivate, and develop a clinical trial team to achieve high performance.
• Provide training and empower team members to take ownership of their responsibilities.
• Monitor team performance and provide coaching to ensure successful delivery of outcomes.
• Ensure team compliance with site-specific policies, procedures, and training requirements.
• Pursue personal development and maintain up-to-date training records.
• Perform additional responsibilities as discussed with the line manager or management.

Key Skills and Requirements

• Strong organizational, planning, and time management skills with attention to detail.
• Ability to multitask and work effectively under pressure.
• Proactive problem-solving skills and confidence in decision-making.
• Excellent stakeholder management and relationship-building abilities.
• Strong written and verbal communication skills.
• High level of integrity, professionalism, and adaptability to changing environments.
• Proven leadership and team development skills.
• Proficiency in clinical assessment techniques and IT systems, including MS Office.
• Solid project management skills to handle multiple projects and resources.
• Tertiary qualifications in health, social, or biological sciences.
• Knowledge of HREC and RGO processes, GCP, and NHMRC guidelines.
• Experience managing clinical studies, preferably in early-phase research.
• Team management experience in a clinical research setting.