Clinical Affairs Program Manager Italy

Experteer Italy; Italia; Remoto; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

An innovative global medical device company is seeking a Clinical Affairs Program Manager for Europe. In this pivotal role, you will lead the execution of clinical trials that showcase the safety and efficacy of groundbreaking medical technologies. With a focus on developing strategies and managing trial approvals, you will collaborate with key stakeholders to ensure successful outcomes. This position offers the flexibility of remote work, combined with the excitement of international travel. If you are a driven professional with a passion for clinical research and a desire to make a significant impact in the medical field, this opportunity is perfect for you.

Competenze

• Minimum 3+ years in clinical management in biopharmaceutical or device industry.
• Expert knowledge of GCP, ICH, ISO guidelines, with FDA experience as an advantage.

Mansioni

• Collaborate with stakeholders to execute clinical trials and manage approvals.
• Develop budgets and ensure compliance with regulatory guidelines.

Conoscenze

Clinical Management

Project Management

Data Management

Biostatistics

GCP Guidelines

Excellent Communication Skills

Team Collaboration

Travel Flexibility

Formazione

BS, BA, BSN or RN in Life Sciences

Strumenti

Electronic Data Capture Systems

Web-based Clinical Trial Management Tools

Descrizione del lavoro

Job Description

Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a Clinical Affairs Program Manager Europe. The role is 100% remote with up to 40% travel and based in Europe.

As part of the global clinical affairs team, you will be responsible for developing strategies for a successful execution of roadmap clinical trials that demonstrate medical product safety and efficacy. Additional responsibilities include management of clinical trials approvals with local IRBs and/or Competent Authorities.

Required Skills and Experience:
1) BS, BA, BSN or RN or higher degree in the Life Sciences or related disciplines
2) Minimum 3+ years in clinical management position in biopharmaceutical or device industry, Clinical Research Organization. Biopharmaceutical experience would provide a strong advantage
3) Additional 4+ years direct experience in clinical trial management
4) Solid track record in successfully executing Phase I – III clinical trials
5) Demonstrated expert knowledge and comprehensive understanding of applicable GCP, ICH, ISO guidelines. Additional FDA and or Health Canada experience would provide a strong advantage but will not be required.
6) Strong, hands-on manager with experience in managing Core Labs, data management, biostatistics, and medical safety reporting
7) Knowledge of electronic data capture systems and web-based clinical trial management tools
8) Excellent interpersonal, written / verbal communication, computer & organizational skills, strong program management and financial skills
9) Excellent command of the English language; both written and verbal. Additional language beside native language is a significant advantage
10) Collaborative team player with strong abilities to operate independently
11) Willing & able to travel domestically and internationally, as required (up to 40%)

Responsibilities:
Collaborate with Company Stakeholders to execute company objectives into successful clinical trials, investigator-sponsored studies, etc.
Overall responsibility for design of clinical trials including protocol development, clinical trial discussions with EU Competent Authorities, and development of timeline and budget
Manage the process of screening/qualifying, selecting, and contracting with investigators, sites and vendors required for conduct of clinical trials
Direct/Manage necessary clinical trial approvals from IRBs/ECs, and ensure studies are on track for site initiation, patient recruitment and enrollment; take corrective actions where necessary to address issues
Develops budget for all clinical projects and adhere to company financial goals
Ensure clinical results are interpreted and documented clearly and concisely for regulatory submissions and publications
Develop, maintain and expand collaborations with Company Stakeholders, clinical investigators and researchers, and key opinion leaders to optimize the clinical development programs
Participate in the development of SOPs and work instructions to assure internal files and clinical study files (patient; site; country) conform to Good Clinical Practice regulations and standards
Ensure adherence to protocols and compliance with regulatory (FDA/ICH/ISO/GCP) guidelines as well as SOP procedures
Identify clinical training needs and develop training materials for in-house and clinical site use