Remote Clinical Trial Manager: CRO & Vendor Lead

Green Key Resources LLC; United States; Remote; USD 90,000 - 140,000; Full time

Job summary

Green Key Resources LLC seeks a Clinical Trial Manager to oversee remote planning, execution, and management of clinical trials in the US. You will collaborate with cross-functional teams and external vendors to ensure on-time, compliant study delivery and robust TMF/CTMS governance.

The role requires 3–4 years of CTM experience, Phase II/III exposure, and strong CRO oversight. Oncology and neuroscience trials are a plus.

Qualifications

• Bachelor’s degree in life sciences, nursing, or related field.
• Minimum 3–4 years of experience as a Clinical Trial Manager.
• Phase II and Phase III trial experience is essential.
• Strong CRO oversight and vendor management skills.
• Proficiency with CTMS, eTMF, EDC, and IRT/IWRS.
• Experience in oncology and neuroscience trials preferred.
• Ability to manage study timelines and operational issues effectively.
• Hands-on experience transitioning trial activities between CROs.
• Strong communication, organizational, and problem-solving skills.

Responsibilities

• Manage day-to-day clinical trial operations and timelines.
• Serve as the primary operational contact for assigned studies.
• Oversee vendor performance and escalate risks as needed.
• Support CRO transitions and ensure documentation transfer.
• Develop and maintain study timelines and budgets.
• Coordinate site startup activities and regulatory document collection.
• Monitor enrollment and implement recruitment strategies.
• Ensure TMF completeness and data system accuracy.
• Manage study closeout activities including site closure and database locks.

Skills

Vendor management

CRO oversight

Timeline management

Cross-functional coordination

Communication

Problem solving

Education

Bachelor’s degree in life sciences or related field

Tools

CTMS

eTMF

EDC

IRT/IWRS

Job description

Green Key Resources LLC seeks a Clinical Trial Manager to oversee remote planning, execution, and management of clinical trials in the US. You will collaborate with cross-functional teams and external vendors to ensure on-time, compliant study delivery and robust TMF/CTMS governance.

The role requires 3–4 years of CTM experience, Phase II/III exposure, and strong CRO oversight. Oncology and neuroscience trials are a plus.