CPM/Sr CPM, IQVIA Biotech CVRM (Cardiovascular, Renal, Metabolic)

Location: Warsaw, Poland; occasional travel to the United States may be required.

Annual base pay: PLN 217,800–404,600, depending on qualifications, experience, location, and schedule.

Company

hirify.global Biotech supports biotech and emerging biopharma companies with clinical development services across phases and therapeutic areas.

What you will do

• Lead the execution and delivery of regional and global clinical studies in line with contracts, timelines, quality standards, and budgets.
• Set objectives for cross-functional project teams, coordinate collaboration, monitor performance, and support milestone achievement.
• Develop integrated study management plans and proactively manage risks, contingencies, issues, and corrective actions.
• Manage customer relationships, stakeholder communications, bid defense participation, and project information reporting.
• Oversee project financials, scope changes, change control, and opportunities to accelerate delivery and revenue.
• Mentor less experienced project team members and contribute to their professional development.

Requirements

• Bachelor’s degree in life sciences or a related field.
• At least 5 years of relevant experience, including more than 1 year of project management experience, or an equivalent combination of education, training, and experience.
• Experience managing regional or global clinical projects and knowledge of clinical trial conduct, ICH GCP, and applicable local regulations.
• Strong written and verbal English communication skills are required.
• Knowledge of clinical protocols, project financials, contractual obligations, planning, prioritization, risk management, and customer communication.
• Ability to work across geographies, collaborate cross-functionally, make decisions, and lead teams toward quality and timeline objectives.

Nice to have

• Experience with cardiovascular, renal, metabolic, or obesity trials.
• Experience with customer presentations, business development collaboration, and mentoring project team members.

Culture & Benefits

• Collaborative, agile environment within an established clinical research organization.
• Work focused on improving project delivery, productivity, quality, financial performance, and customer satisfaction.
• Opportunity to support innovative treatments across biotech and emerging biopharma programs.
• Health, welfare, incentive, bonus, and other benefits may be offered depending on the position.