Senior Clinical Project Manager

This is a fully remote position, open to applicants in Florida, +1 more state.

📋 Description

• Accountable for independently directing the clinical trial study team.

• Overseeing global clinical trial operations on pivotal studies.

• Effectively communicates and mentors clinical team members.

• Collaborates efficiently with R&D, Regulatory, Quality, and Marketing/Product stakeholders.

• Manages all clinical studies, including the development of project management plans.

• Identifies, qualifies, and trains investigators and teams.

• Responsible for activities related to IRBs/ECs and clinical study vendors.

• Proactively manages the data management and data lock processes.

• Establishes strong relationships with the Principal Investigator and coordinator.

⛳️ Requirements

• Bachelor’s degree in a Life Sciences discipline is required.

• Exceptional command of professional English, with advanced skills in medical and scientific writing.

• Proven experience in authoring clinical study protocols.

• Strong skills in presentation and communication.

• Comprehensive understanding of the medical device clinical trial lifecycle.

• In-depth knowledge of medical device clinical research.

• Solid grasp of biostatistics and clinical data interpretation.

• Minimum of 5–6 years of progressive experience in clinical project management.

• Experience working directly with regulatory authorities.

• Demonstrated ability to manage and supervise external clinical vendors.

• Excellent organizational, leadership, and stakeholder management abilities.

🏝️ Benefits

• Competitive perks and benefits.