Clinical Project Manager

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

📋 Description

• Take the lead on clinical projects independently, ensuring alignment with the study budget and scope of work.

• Utilize your interpersonal and organizational expertise to establish and accomplish objectives in project execution, encompassing both contractual and financial goals.

• There may be opportunities to manage international trials as well.

• Act as the primary liaison with clients, delivering exceptional customer service, which includes engaging in proposal activities and client presentations.

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

• Oversee and manage all facets of clinical research trials.

• Ensure comprehensive project management across all functional areas, including data management, safety, clinical, medical monitoring, and biostatistics.

• Generate project status updates for clients and management, highlighting key deliverables and success metrics, as well as escalation points.

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

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

⛳️ Requirements

• A degree or a similar 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.

• 5 to 7 years of industry experience, including at least 4 years of full-service Project Management experience in a clinical trial setting within a Clinical Research Organization.

• Experience in managing studies in the Oncology domain.

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

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

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

• Strong presentation capabilities.

• Demonstrated computer proficiency (MS Office, MS Project, PowerPoint) and experience with software (CTMS, eTMF, EDC, IXRS).

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

• A solid understanding of medical terminology and clinical trial operations as they pertain to executing a clinical development plan.

🏝️ Benefits

• We provide an exciting, high-energy environment with dedicated and collaborative team members who relish challenges, excel in detail-oriented tasks, and thrive in dynamic settings.

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