Remote Senior Clinical Trial Lead

Precision Medicine Group; Northern (KY); Hybrid; USD 111,000 - 201,000; Full time

Benefits offered by this job

Discretionary annual bonus

Health insurance

Retirement savings benefits

Life insurance

Disability benefits

Parental leave

Paid time off (Sick leave and vacation

Job summary

Precision Medicine Group is seeking a Clinical Trial Manager/Senior Clinical Trial Manager to lead planning, conduct, and oversight of clinical studies in the United States. This remote role requires close collaboration with PMs, CRAs, and regulatory teams to ensure protocol adherence and high-quality deliverables.

The candidate will craft clinical plans, templates, training materials, conduct feasibility analyses, and drive site initiation and enrollment strategies while maintaining GCP/SOP

Qualifications

• Bachelor’s degree or equivalent in science/health; advanced degree preferred.
• Minimum 7 years of clinical research experience or comparable oversight experience.

Responsibilities

• Serve as the clinical trial lead for planning, conduct and oversight of studies.
• Collaborate on monthly invoicing and variance management of the clinical budget.
• Develop study documents, CRF guidelines, training materials, and study trackers.
• Identify training needs for CRAs and vendors; present at Investigator Meetings and Kick-offs.
• Drive site feasibility through stakeholder input and country recruitment/retention strategy.
• Develop robust communication with investigators and study teams to ensure timelines and quality.

Skills

Clinical trial management

Excellent communication & teamwork

Project budgeting & invoicing

Education

Bachelor’s degree or equivalent in science/health

Advanced degree preferred

Tools

Microsoft Office

Job description

Precision Medicine Group is seeking a Clinical Trial Manager/Senior Clinical Trial Manager to lead planning, conduct, and oversight of clinical studies in the United States. This remote role requires close collaboration with PMs, CRAs, and regulatory teams to ensure protocol adherence and high-quality deliverables.

The candidate will craft clinical plans, templates, training materials, conduct feasibility analyses, and drive site initiation and enrollment strategies while maintaining GCP/SOP