Clinical Project Manager – Regional or Global Experience

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

📋 Description

• Oversees interdisciplinary clinical research studies as a project manager.

• Ensures adherence to Good Clinical Practice (GCP), relevant Standard Operating Procedures (SOPs), and regulatory guidelines.

• Serves as the primary point of contact between the Company and the Client to guarantee timely initiation, execution, and completion of studies in line with contractual agreements.

• Leads the project team to ensure quality, adherence to timelines, and effective budget management.

• Responsible for the financial outcomes of each project.

• Coordinates the activities and deliverables of all study partners, while proactively identifying and addressing issues.

• Guarantees that studies are conducted in accordance with GCP, relevant SOPs, and regulatory standards.

• Accountable for the successful delivery of all project outputs for assigned projects.

• Oversees the quality and thoroughness of the Trial Master File (TMF) for assigned projects.

• Responsible for the upkeep of study information across various databases and systems.

• Manages study components related to inspection readiness across all aspects of study conduct.

• Provides oversight for the creation and execution of project plans.

• Plans, organizes, and presents at both internal and external meetings.

• Prepares project management reports for clients and internal management.

• Cultivates strong relationships with existing clients to foster future business opportunities.

• May be involved in bid defense meetings where they are presented as the potential project manager.

⛳️ Requirements

• Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or a related field combined with relevant experience.

• Preferred experience in a Clinical Research Organization (CRO) and within relevant therapeutic areas.

• In-depth understanding of Good Clinical Practice/ICH guidelines and other applicable regulatory standards.

• Strong organizational abilities.

• Excellent time management skills and capacity to work independently.

• Direct expertise in the therapeutic area.

• Willingness to adopt new technologies.

• Outstanding communication, presentation, and interpersonal abilities, both written and verbal.

• Flexibility to travel as needed (approximately 25%).

🏝️ Benefits

• We are dedicated to nurturing our employees through career growth and advancement;

• supportive and engaged leadership;

• training in technical and therapeutic areas;

• peer recognition and a comprehensive rewards program.

• We are committed to fostering an inclusive culture where you can truly be yourself.