Senior Clinical Project Manager – Oncology

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

📋 Description

• Take charge of clinical projects independently, ensuring adherence to the study budget and scope of work.

• Establish and meet objectives for project execution, encompassing contractual and financial goals.

• Execute international trials as necessary.

• Act as the primary contact for clients, delivering exceptional customer service.

• Engage in proposal activities and deliver client presentations.

• Coordinate with project teams and senior management at Precision, as well as with sponsor organizations, including C-level stakeholders.

• Oversee and manage all facets of clinical research trials.

• Supervise all functional areas, such as data management, safety, clinical, medical monitoring, and biostatistics.

• Prepare project status reports for clients and management.

• Identify critical deliverables, success metrics, and escalation requirements.

• Actively contribute as a Project Team member to facilitate efficient trial management and implementation.

• Draft and review protocols and study documentation, including project plans, informed consents, site contracts, and budgets.

• Manage client relationships, project teams, budgets, timelines, scope, costs, and quality throughout the study lifecycle.

⛳️ Requirements

• A degree or a similar relevant qualification in life sciences, or an equivalent combination of education and experience.

• Essential previous experience in a full service/global Project Management role within the CRO industry.

• Extensive background in Clinical Operations within a CRO setting.

• Minimum of 4 years of full service Project Management experience in a clinical trial environment at a Clinical Research Organization.

• Experience in managing studies related to Oncology.

• Familiarity with GCP/ICH guidelines and the clinical development process.

• Willingness and ability to travel domestically and internationally, including overnight stays.

• Proficient written and verbal communication skills in English.

• Strong presentation abilities.

• Demonstrated computer proficiency in MS Office, MS Project, and PowerPoint.

• Experience with CTMS, eTMF, EDC, and IXRS software.

• Proven capability to foster positive working relationships with individuals and teams both internally and externally.

• A solid understanding of medical terminology and clinical trial activities as they pertain to the execution of a clinical development plan.

• Legally authorized to work in the country of employment without the need for employer sponsorship.

🏝️ Benefits

• Supportive and collaborative work environment.

• Emphasis on work-life balance.

• Opportunities for team development.

• Chance to work with a global team.

• Commitment to equal opportunity employment.

• Reasonable accommodations available for applicants with disabilities.