Associate Clinical Research Specialist

Medtronic; Milano; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A global healthcare technology company is seeking a candidate to support scientific projects in the Milan office. This role involves monitoring trial progress, collaborating with teams, and developing communication materials. Applicants should have a Bachelor’s or Master’s degree in a scientific field and at least 2 years of experience in clinical research. This position offers a hybrid work model and competitive compensation.

Servizi

Competitive salary

Flexible benefits package

Competenze

• At least 2 years of experience in clinical research, medical writing, or scientific communication.
• Ability to manage multiple projects and meet deadlines independently.
• Proficiency in additional languages and a background in clinical affairs are desirable.

Mansioni

• Support in the design and implementation of the Scientific project.
• Monitor trial progress and conduct site visits.
• Develop presentations and communication materials for stakeholders.
• Contribute to the development of training materials for clinical staff.

Conoscenze

Analytical and problem-solving abilities

Detail-oriented

Excellent written and verbal communication skills

Strong collaboration skills

Formazione

Bachelor’s or Master’s degree in a scientific field

Descrizione del lavoro

Overview

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. This role is a short-term contract based in the Milan office, with a hybrid work model and minimal travel requirements (approximately 5% of the time).

Responsibilities

• Support in the design and implementation of the Scientific project in compliance with GCP and regulatory standards.


• Contributes to scientific projects, with close supervision, using specialized knowledge and skills.


• Monitor trial progress, conduct site visits, and ensure adherence to SOPs and timelines.


• Oversee budgets, timelines for assigned projects.


• Collaborate with cross-functional teams.


• Translate complex clinical data into clear, compelling messages for diverse audiences.


• Develop presentations and communication materials for internal and external stakeholders.


• Contribute to the development of training materials and educational content for clinical staff.


• Support in the preparation, review and filing of clinical study documents including protocols, investigator brochures, informed consent forms, and final study reports.


• Draft scientific manuscripts, abstracts, and posters for publication and presentation.


• Ensure clarity, accuracy, and scientific integrity in all written materials.


• Support regulatory submissions with well-documented and compliant content.


• Review, summarize, and maintain databases of peer-reviewed and internally created scientific literature.


• Report complaints or adverse events identified in the literature to Global Clinical Health (GCH).


• Prepare responses to audit and submission queries.


• May collaborate with external healthcare professionals to develop scientific content.

Required Knowledge and Experience

• A Bachelor’s or Master’s degree in a scientific field.


• Excellent written and spoken English.


• Analytical and problem-solving abilities.


• Detail-oriented with organizational skills.


• Excellent written and verbal communication skills.


• Ability to synthesize scientific data and communicate effectively.


• At least 2 years of experience in clinical research, medical writing, or scientific communication.


• The ability to perform literature reviews.


• Ability to manage multiple projects and meet deadlines independently.


• Strong collaboration skills to work effectively in a global, multidisciplinary team.


• Flexibility and proactivity.


• Medical Writing certifications, Project Management skills, proficiency in additional languages, and a background in clinical affairs are desirable qualities for this role, enhancing the ability to manage projects efficiently, navigate regulatory requirements, and communicate effectively in a global healthcare environment.

Physical Job Requirements

The statements describe the general nature and level of work performed by employees in this position and are not an exhaustive list of all responsibilities and skills.

Benefits & Compensation

Medtronic offers a competitive salary and flexible benefits package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here