Responsibilities:

• Oversee all clinical trial activities.
• Prepare and submit regulatory documentation for study approval.
• Negotiate contracts and budgets with clinical sites.
• Manage contract research organizations (CROs).
• Provide support and training to clinical sites.
• Recruit and motivate patients for clinical trials.
• Maintain communication with clinical sites.
• Hire and manage clinical specialists and field engineers.
• Manage clinical supplies.

Qualifications:

• Minimum 5 years clinical operations experience in medical device industry.
• Strong communication and interpersonal skills.
• Proven project management abilities.
• Knowledge of regulatory processes.
• Fluency in English.
• Basic technical proficiency.
• Ability to travel extensively.
• Bachelor’s or Master’s degree in life sciences, medicine, or related field.