Impactful Clinical Project Manager – 12-Month Contract

GForce Life Sciences; Plano (TX); Sur place; USD 85 000 - 120 000; Plein temps

Avantages offerts par ce poste

Medical, Dental, Vision

Résumé du poste

GForce Life Sciences is seeking a results-oriented Clinical Project Manager to oversee multi-site trials and ensure on-time, within-budget delivery. You will coordinate cross-functional teams, manage timelines, and supervise regulatory submissions with oversight from Regulatory Affairs.

Responsibilities include protocol input, budget tracking, vendor management, and maintaining study quality. The role is 4 days onsite across Plano, Maple Grove, Santa Clara, Sylmar, CA and other sites, with a

Qualifications

• Minimum of 2 years clinical project management experience.
• Minimum of 3-5 years in clinical trials.
• IDE experience required.

Responsabilités

• Facilitates communication across R&D, Regulatory Affairs, Sales and Marketing, Training and Senior Management.
• Manages clinical study timelines and budget using project tools.
• Coordinates investigator and research coordinator meetings.
• Oversees compliance to study requirements and protocol.
• Coordinates activities for milestones like database locks and annual reports.

Connaissances

Clinical project management

Project coordination

Formation

Bachelor's degree in Health Sciences

Outils

IDE experience

Description du poste

GForce Life Sciences is seeking a results-oriented Clinical Project Manager to oversee multi-site trials and ensure on-time, within-budget delivery. You will coordinate cross-functional teams, manage timelines, and supervise regulatory submissions with oversight from Regulatory Affairs.

Responsibilities include protocol input, budget tracking, vendor management, and maintaining study quality. The role is 4 days onsite across Plano, Maple Grove, Santa Clara, Sylmar, CA and other sites, with a