Associate Clinical Trial Manager (Phd) - Infectious Disease / Immunology

Medpace; Monza; In loco; EUR 65.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored events

Health and wellness initiatives

Descrizione del lavoro

Medpace is seeking an Associate Clinical Trial Manager to help oversee global trial activities, coordinating study timelines, quality control, and stakeholder communications to advance cutting-edge therapeutics. This entry-level position offers intensive training, international exposure, and a clear path toward advanced CTM responsibilities.

You will work in a fast-paced, collaborative team with opportunities to grow within the clinical trial management field and contribute to meaningful patient

Competenze

• PhD in Life Sciences required or preferred.
• Fluency in English with strong presentation skills.
• Ability to work in a fast-paced, international team.
• Experience in CRO or pharmaceutical industry is advantageous but not required.

Mansioni

• Coordinate study timelines and project milestones.
• Perform quality control of trial activities and deliverables.
• Maintain and communicate status reports to CTM team and sponsors.
• Interact with internal project teams, Sponsors, sites and vendors.
• Oversee regulatory filing processes and study supplies.
• Create and maintain project timelines and meeting minutes.

Conoscenze

Strong communication

Team collaboration

Ability to work under pressure

Clinical trial management

Regulatory filing processes

Formazione

PhD in Life Sciences

Descrizione del lavoro

As an Associate Clinical Trial Manager at Medpace, you join the Clinical Trial Management team to help oversee global trial activities and ensure timely, accurate execution. You will collaborate with project coordinators, clinical trial managers, sponsors, and sites, applying your analytical and academic background to clinical project administration. This role offers intensive training, international exposure, and a clear path toward advanced CTM responsibilities. You’ll work on coordinating study timelines, quality control, and stakeholder communications to advance cutting-edge therapeutics. This is a hands‑on entry into industry with meaningful impact on patient outcomes.

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Communicate and collaborate on global study activities with project coordinator and clinical trial manager
• Ensure timely delivery of recurring tasks with high accuracy
• Compile and maintain project-specific status reports in the CTM system
• Interact with internal project team, Sponsor, study sites, and third-party vendors
• Manage and perform quality control of the internal regulatory filing system
• Provide oversight and management of study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes
• PhD in Life Sciences
• Fluency in English with strong presentation skills
• Ability to work in a fast‑paced, international team
• Prior CRO or pharmaceutical industry experience is advantageous but not required
• strong communication
• team collaboration
• ability to work under pressure
• clinical trial management
• regulatory filing processes

Associate Clinical Trial Manager (PhD) - Infectious Disease / Immunology monza-brianza, lombardia, it