Clinical Project Manager / Senior Clinical Project Manager

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

📋 Description

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

• Utilize your exceptional interpersonal and organizational skills to establish and meet objectives for project execution, encompassing both contractual and financial goals.

• Act as the main point of contact for clients, delivering outstanding customer service, which includes involvement in proposal activities and client presentations.

• Collaborate with the Project Team and senior management from both Precision and sponsors, including C-level executives.

• Manage all aspects of clinical research trials effectively.

• Oversee total project management across all functional areas, including data management, safety, clinical operations, medical monitoring, and biostatistics.

• Prepare project status updates for clients and management, highlighting key deliverables, performance metrics of success, and escalation points.

• Actively participate as a member of the Project Team, aiming to enhance the management and execution of trials.

• Draft and review protocols and other essential study documents, such as project plans, informed consents, site contracts, and budgets.

⛳️ Requirements

• A degree or a related qualification in life sciences, or a comparable combination of education and experience.

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

• Extensive experience in Clinical Operations roles within a CRO, with a minimum of 4 years of full-service Project Management experience in a clinical trial environment for a Clinical Research Organization.

• Experience managing studies in the field of Oncology.

• Working knowledge of GCP/ICH guidelines and the clinical development process.

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

• Proficient communication skills in English, both written and spoken.

• Strong presentation abilities.

• Proven computer skills (MS Office, MS Project, PowerPoint) and experience with software such as CTMS, eTMF, EDC, and IXRS.

• Demonstrated 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 executing a clinical development plan.

🏝️ Benefits

• We provide a vibrant, high-energy environment with dedicated, collaborative team members who relish a challenge, excel in details, and thrive in dynamic settings.

• A supportive and collaborative workplace that promotes work-life balance and encourages team development.

• Opportunities for growth and career advancement.

• Positive teamwork aimed at delivering exceptional results.