Clinical Trial Manager

• Four or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.
• Previous SSU and Clinical Trial Lead experience
• Comprehensive knowledge of GCP, ICH, and regulatory guidelines.
• Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).
• Effective leadership in remote and global environment.
• Strong communication, planning, and organizational abilities.

• University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Fluent in English, both written and verbal

Master’s or other advanced degree.

PMP certification or equivalent.

Physical Demands / Work Environment:

• Remote-based work required with possible office presence depending on location.
• Travel requirements: up to 20% (global – primarily domestic and international)
• Proficiency in balancing concurrent tasks within time-sensitive environments.
• Financial awareness and use of tracking systems/tools.
• Demonstrated independent problem-solving and risk management mindset.
• Demonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.
• employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training
• without altering the fundamental nature or classification of the position.