Remote Senior Clinical Study Manager

Penfield Search Partners Ltd.; Fairfield (CT); Remote; USD 140,000 - 190,000; Full time

Job summary

Penfield Search Partners Ltd. is seeking aSr. Clinical Study Manager to lead end-to-end clinical operations for pre-clinical and diagnostic trials.

You will oversee planning, budgeting, resource allocation, and CRO coordination while guiding staff across cross-functional teams to meet timelines and quality standards. The role requires 8+ years in clinical research within medical devices, IVD, biotech, or pharma and strong regulatory knowledge.

Qualifications

• Bachelor’s degree in a scientific discipline or equivalent experience.
• 8+ years of clinical research within medical devices, IVD, biotech, or pharma.

Responsibilities

• Oversee full scope of clinical studies from planning through completion.
• Lead Clinical Operations staff and manage CRO activities as needed.
• Develop study budgets and timelines with risk mitigation plans.
• Ensure regulatory compliance and high-quality study documentation.
• Provide regular leadership updates on milestones, budget, and performance.

Skills

Leadership

Cross-functional collaboration

Regulatory knowledge

Clinical research experience

Technical writing

Education

BSc or equivalent (scientific field)

Job description

Penfield Search Partners Ltd. is seeking aSr. Clinical Study Manager to lead end-to-end clinical operations for pre-clinical and diagnostic trials.

You will oversee planning, budgeting, resource allocation, and CRO coordination while guiding staff across cross-functional teams to meet timelines and quality standards. The role requires 8+ years in clinical research within medical devices, IVD, biotech, or pharma and strong regulatory knowledge.