Clinical Research Manager

TN Italy; Italia; In loco; EUR 50.000 - 90.000; Tempo pieno

Descrizione del lavoro

An innovative company is seeking a Clinical Research Manager to oversee medical device clinical trials in Europe. This role involves managing multi-center studies while ensuring compliance with Good Clinical Practices and regulatory guidelines. The ideal candidate will possess strong leadership and communication skills, with a proven track record in clinical affairs and the ability to foster relationships with site investigators. Join a forward-thinking team dedicated to advancing healthcare solutions and making a significant impact in the medical device industry.

Competenze

• 3+ years of experience in the medical device arena.
• Familiar with catheter lab/operation room environment.
• Excellent written and oral English communication skills.

Mansioni

• Manage and provide accountability for day-to-day operations of clinical studies.
• Serve as primary Sponsor contact for operational project-specific issues.
• Conduct periodic site visits for engagement and management.

Conoscenze

Leadership Skills

Communication Skills

Organizational Skills

Problem-Solving Skills

Clinical Affairs Experience

Technical Skills

Formazione

Bachelor’s degree in a health-related field

Advanced degree in a health-related field

Descrizione del lavoro

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The Company is currently seeking a Clinical Research Manager which will be located in Europe. Reporting to the company R&D manager and will be responsible for clinical operational oversight and execution (initiation, enrollment, and completion) of the medical device clinical trials.

The CTM will manage the assigned clinical trial(s) in adherence to Good Clinical Practices as applicable under the regulatory agency(ies) governing the study, and any other applicable guidelines and regulations.

The CTM is responsible for independently managing a range of activities for multi-center, medical device clinical studies in Europe. This position requires strong leadership skills and the ability to manage people, meet clinical project goals and timelines, and in alignment with company initiatives.

Main Responsibilities

• Responsibility of new studies with the company product: site selection and installation, materials, submissions, contracts, EDC, etc.
• Manage and provide accountability for the day-to-day operations of the study, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations.
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables.
• Maintain in-depth knowledge of protocol, therapeutic area, and indication.
• Establish strong relationships with site investigators and other KOLs.
• Conduct periodic site visits (engagement and management).

Qualifications

• Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
• 3+ years of experience in the medical device arena
• 3+ years of Clinical Affairs/field clinical specialist
• Familiar with catheter lab/operation room environment
• Experience with a mid-scale US or EU Pivotal Trial
• Excellent written and oral English communication skills
• Good organizational and technical skills
• CT reading / ECG analysis – an advantage
• Overseas travel up to 20%

Personal skills:

• Excellent communication, presentation, interpersonal and problem-solving skills
• Ability to work independently as well as collaboratively in a start-up environment
• Work under time and pressure constraints