Clinical Study Operations Manager

Beacon Biosignals, Inc.; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

Beacon Biosignals, Inc. is recruiting a full-time Clinical Study Operations Manager to oversee clinical study operations, ensuring compliance and effective execution of projects in both remote and onsite environments.

This role supports precision medicine initiatives and requires strong leadership in a matrix environment. You will lead planning, execution, and monitoring of trials, ensure adherence to regulatory guidelines, and coordinate with quality, data management, and clinical teams to

Qualifications

• Bachelor's degree in life sciences or related field
• Experience in clinical operations management in biotech or pharmaceutical setting
• Strong understanding of regulatory guidelines and clinical trial processes
• Proven ability to manage multiple projects and meet deadlines
• Experience with EEG or neurological studies is a plus

Responsibilities

• Manage and coordinate clinical study operations, including planning, execution, and monitoring of studies
• Ensure compliance with regulatory requirements and company policies throughout the study lifecycle
• Collaborate with cross‑functional teams to optimize study design and execution strategies

Job description

To support innovative clinical development in precision medicine, the full-time Clinical Study Operations Manager will oversee clinical study operations, ensuring compliance and effective execution of projects in both remote and onsite environments.

Key responsibilities

• Manage and coordinate clinical study operations, including planning, execution, and monitoring of studies
• Ensure compliance with regulatory requirements and company policies throughout the study lifecycle
• Collaborate with cross‑functional teams to optimize study design and execution strategies

Required qualifications

• Bachelor's degree in life sciences or a related field
• Experience in clinical operations management, preferably in a biotech or pharmaceutical setting
• Strong understanding of regulatory guidelines and clinical trial processes
• Proven ability to manage multiple projects and meet deadlines
• Experience with EEG or neurological studies is a plus