Careers that Change Lives
Contribute to offering Medtronic business units services that support their clinical operations at an outstanding quality and efficiency level, contributing to their strategies for worldwide medical device approvals to introduce new products to market.
In this role as a Associate Clinical Report Development Specialistist in MC2 Solutions development, your core responsibilities will be providing report design and development support for MC2’s core internal forecasting and demand management team, partnering with your teammates to secure our services meet the needed level of quality, accuracy, and availability.

In addition, you will contribute to offer our stakeholder report development and business intelligence solutions applied to clinical trials conduct, allowing the team to continue meeting expectations from our internal stakeholders.
Come for a job, stay for a career.
Our Department
Medtronic Core Clinical Solutions (MC2) function offers support to clinical studies from all Medtronic Operating Units globally, offering to internal partners services that span across all stages of operation a clinical trial conduct, from designing and building data collection systems to partnering with statisticians in conducting analyses, through conducting monitoring activities at the hospitals and tracking adverse events and ensuring regulatory requirements on safety reporting are met.

As part of MC2, Global Clinical Data Solutions (GCDS) offers Data Management, Solutions Development and Statistical Programming services to our partners, supporting the design and build of data collection systems, of reporting and dashboarding solutions, and statistical analysis routines.
It also offers technical support and business analisys expertise in the technology and IT domain to other MC2 functions and Medtronic stakeholders.

Tasks & Responsibilities
The Associate Clinical Report Development Specialistist is responsible for applying development expertise and understanding of clinical processes to the development of reports and custom components as needed to support clinical trials.

• Supports or executes clinical data and operational reports
• Interacts with internal Data Solutions (Clinical Data Specialists and Statistical Programmers) colleagues, other MC2 partners and possibly business partners including clinical study teams, Global IT, business strategists, and statisticians
• May support and/or work with additional project teams, disciplines, or functions within Medtronic
• Understands the design, develops, and tests (under supervision or guidance) Clinical Reports, System Interfaces, Clinical Data Transfers or other components related to clinical studies
• Understands and utilizes, under guidance, industry standards to contribute to defining and implementing reporting standards for the development team
• Supports other Clinical Report Development Specialists on planning, designing, and implementing Clinical Reports, System Interfaces, Clinical Data Transfers, or other components.
• Assists,under supervision, as clinical technical specialists in the planning, designing, and implementing of clinical applications
• May assist with technical consultation on and task direction for vendors
• Reviews and acknowledges all Standard Operating Procedures and other quality requirements assigned to the job role.

Must Haves
• 0-2 Years relevant working experience with with Masters degree in Biomedical Engineering, with an academic track strongly focused on clinical data and/or informatics as advantage
• Beginning to intermediate level of proficiency with relational databases and clinical operations data, preferably Microsoft SQL Server or ORACLE.
• Beginning to intermediate level of proficiency programming SQL language.
• Detail-oriented view of reporting processes, tools and procedures.
• Good problem-solving skills;
• Client and customer focused in all aspects;
• Team player skills;
• Good communication skills.
• Good English language skills in reading, writing and speaking;

Nice to Haves
• 0-2 Years relevant working experience with with Masters degree in Biomedical Engineering, with an academic track strongly focused on clinical data and/or informatics as advantage
• Basic to intermediate knowledge of other programming languages (e.g. python, .NET, C#, java, R, SAS, etc.).
• Knowledge of the systems development life cycle and relational databases
• Awareness of ICH/GCP/FDA regulations and guidelines as they pertain to clinical systems including 21 CRF Part 11
• Reporting experience in a clinical research environment
• Report development practices and validation

We Offer
In our 5th Tenet of our Mission we recognize the personal worth of employees by providing an employment framework that allows personal satisfaction in work accomplished, security, advancement opportunity, and means to share in the company's success.
Also a competitive package is of course part of that. We offer a competitive salary and benefits package to all our employees:
• Flexible working environment;
• Annual Incentive Plan % depending on company results;
• Pension scheme and group discount on healthcare insurances;
• Training possibilities via Cornerstone/Harvard Manage Monitor/GetAbstract;
• Employee Assistance Program and Recognize! (our global recognition program).

This position is fixed-termfor 1 year, can be prolongate.

Your Answer
Is this the position you were waiting for? Then please apply directly via the apply button!

About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.
We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team.
Let’s work together to address universal healthcare needs and improve patients’ lives.Help us shape the
future.

Founded in 1949 as a medical repair company, we're now among the world's largest medical technology, services and solutions companies, employing more than 86,000 people worldwide, serving physicians, hospitals and patients in over 155 countries.

Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your own career. Join us in our commitment to take healthcare Further, Together.

Founded in 1984, APCO Worldwide is an award-winning, independently owned global communication and business strategy firm with offices in major cities throughout North America, Europe, the Middle East and Asia. APCO combines a global perspective with local expertise to help clients around the world manage challenges, opportunities, perceptions and reputations. APCO clients include corporations and governments; industry associations and nonprofit organizations; and many of the top companies on the Fortune 500. The firm is a majority women-owned business.

About APCO in Italy

APCO’s multilingual team helps clients navigate the complex policy, regulatory and media landscape in Italy, one of the largest European markets, which is currently developing a number of ambitious economic and institutional reforms to re-launch the local economy. Our Italy team, with offices in Rome and Milan, is fully integrated with APCO’s global operations and offers clients cross-sector services, empowered by an in-depth knowledge of the national landscape and a strong network of media and institutional contacts.

APCO was awarded Best Agency to Work for: EMEA Network in 2017 and 2019 and EMEA Corporate Consultancy of the year, 2019 by the PRovoke Media.

The opportunity:
As a Consultant/Senior Consultant, you will work closely with colleagues at all levels on research, writing, media, and creative problem-solving. You will be involved in day-to-day support of client projects by supervising draft materials prepared from more junior staff (i.e. press releases, Q&A, position papers, etc.), monitoring media, and by conducting and analyzing research on a variety of client-related issues or on business development efforts.

You’ll have the opportunity to work across disciplines, including corporate communication, crisis and issues, corporate social responsibility, media relations, stakeholder and KOL engagement, and digital/social media. A specific expertise on Healthcare subjects and a capability to navigate the Healthcare market is required. 

For a Consultant these are typical examples of work:

• Supporting the implementation of a wide range of strategic communication projects and campaigns for our high-profile, globally recognized clients
• Supporting the design and implementation of integrated campaigns to position client issues and priorities them upon key audiences that may include elected officials, media, key opinion leaders, consumers and industry stakeholders
• Creating effective messages and editing high-quality written deliverables, such as briefings, press materials, and social media content often under tight deadlines
• Owning stakeholders/media relations, fostering relationships with media, drafting talking points, organizing events/webinars/press conferences
• Monitoring external developments in key client issue areas and flag opportunities for further client engagement
• Participating in business development activities including writing proposals and developing pitch decks
• Attending and participating in internal and client meetings, including brainstorming sessions
• Mentoring and driving the work of interns and more junior staff

For a Senior Consultant these are typical examples of work:

• Managing portions of large clients projects or small clients projects independently
• Managing on a macro level the work of more junior colleagues, providing feedback and ensuring the quality of work
• Completing client deliverables under the supervision of the assigned account manager
• Supporting the complete approval of proposals, showing strategic thought, scope of work and pricing awareness
• Maintaining an awareness of macro business issues impacting clients, by conducting and analyzing research on a variety of client related issues.
• Independently coordinating client meetings and events
• Maintaining independent contacts with clients without requiring a supervisor support

The ideal candidate for the Consultant level will be / have:

• Degree from an accredited college or university in a related field
• Proficiency in both written and spoken English
• Ideally a minimum of 3-5 years of Pr, strategic communications or media experience – agency experience is a plus. Healthcare expertise is required
• Solid management experience and a proven ability to juggle multiple projects, client initiatives and teams of junior colleagues in a fast-paced environment
• Previous experience developing and supporting strategic communications plans (corporate, issues management, internal communications, crisis communications, etc.) within the Healthcare market
• Able to demonstrate exceptional presentation, writing and analytical skills, including experience writing strategic plans, messaging and press materials and the ability to write both strategically and creatively under tight deadlines
• Excellent client and interpersonal skills

The ideal candidate for the Consultant level will be / have:

• Degree from an accredited college or university in a related field
• Proficiency in both written and spoken English
• Ideally, a minimum of 5-7 years of Pr, strategic communications or media experience – agency experience is a plus. Healthcare expertise is required
• Solid project management experience and a proven ability to manage multiple projects and client initiatives and teams of both junior and senior colleagues in a fast-paced environment
• Previous experience developing and supporting strategic communications plans (corporate, issues management, internal communications, crisis communications, etc.) within the Healthcare market
• Able to demonstrate exceptional writing and analytical skills, including experience writing strategic plans, messaging and press materials and the ability to write both strategically and creatively under tight deadlines
• Excellent client and interpersonal skills; ability to manage independent client relationships and communicate effectively by phone, email, and in-person
• Strong presentation skills

We are pleased to meet you. We are Galapagos, a dynamic, fast growing biotech company with offices in Europe in Belgium (Mechelen), France (Romainville), the Netherlands (Leiden), Switzerland (Basel), Germany (Munich), Great Britain (London) and in the USA (Boston).

Our job is to change the lives of our fellow human beings. In our quest to discover and develop life-enhancing drugs, we venture into completely unexplored territory. We see new opportunities in every challenge we are faced with. We want to try the impossible. We need thought leaders and quick thinkers, people with an entrepreneurial spirit who are not satisfied with the status quo. We need cooperative innovators and tireless idealists. We need the best in class. In other words, we need you: the “doers”.

Due to our exciting collaboration with Gilead Sciences, we are looking for the Medical Science Liaison Manager in Italy.

Are you ready to conquer the world and shape the future together with us?

Scope of work

• Act as leader by mentoring, coaching and developing MSL's to fulfill their potential, while also delivering business objectives.
• Be a scientific expert in Inflammation and Rheumatology and is responsible for assessing the condition of the disease and solely in hindsight our products, patient treatment trends and studies in the areas in which we operate are to discuss on a peer-to-peer basis with a defined audience of external clinical and non-clinical stakeholders (doctors, pharmacists, hospital managers, board members of scientific societies and other stakeholders) in accordance with the general stakeholder mapping and as a trustworthy one to be regarded as a scientific contact and partner.
• The MSL role is field-based. They serve as a field-based extension of the Medical Affairs team. 
• Through scientific interactions, you will gain valuable insight into treatment patterns and scientific activities in the field of inflammation and Rheumatology and you will provide strategic input to the company's medical affairs plan.
• Through scientific interactions with external stakeholders, you increase the medical value of our products, based on the risk-benefit profile of our drugs, and contribute to the promotion of innovative therapeutic approaches for patients.

Who are you?

• You have a higher degree in Life Sciences (MD, PharmD, or PhD or equivalent) is required
  
• You have great experience as MSL in the field and more than 3 years of line management experience
  
• You have a solid track record of effective and influential oral presentations within the healthcare / science industry
  
• You have excellent people management skills
• You have proven medical, clinical, or research experience in inflammation and rheumatology
  

What's in it for you?

You become part of a fast growing amazing company. As a “doer” you receive all the support you need to carry out your work successfully. Galapagos strives to recruit the best people who set themselves apart through integrity and excellent interpersonal and organizational skills. Our people are the strength of Galapagos, a highly motivated team dedicated to maintaining the Galapagos leadership position and making breakthroughs in pharmaceutical research. Galapagos offers a competitive compensation package and a dynamic work environment.

We are Galapagos: together we can do it!

We are pleased to meet you. We are Galapagos, a dynamic, fast growing biotech company with offices in Europe in Belgium (Mechelen), France (Romainville), the Netherlands (Leiden), Switzerland (Basel), Germany (Munich), Great Britain (London) and in the USA (Boston).

Our job is to change the lives of our fellow human beings. In our quest to discover and develop life-enhancing drugs, we venture into completely unexplored territory. We see new opportunities in every challenge we are faced with. We want to try the impossible. We need thought leaders and quick thinkers, people with an entrepreneurial spirit who are not satisfied with the status quo. We need cooperative innovators and tireless idealists. We need the best in class. In other words, we need you: the “doers”.

Due to our exciting collaboration with Gilead Sciences, we are looking for the Medical Science Liaison Manager in Italy.

Are you ready to conquer the world and shape the future together with us?

Scope of work

• Act as leader by mentoring, coaching and developing MSL's to fulfill their potential, while also delivering business objectives.
• Be a scientific expert in Inflammation and Rheumatology and is responsible for assessing the condition of the disease and solely in hindsight our products, patient treatment trends and studies in the areas in which we operate are to discuss on a peer-to-peer basis with a defined audience of external clinical and non-clinical stakeholders (doctors, pharmacists, hospital managers, board members of scientific societies and other stakeholders) in accordance with the general stakeholder mapping and as a trustworthy one to be regarded as a scientific contact and partner.
• The MSL role is field-based. They serve as a field-based extension of the Medical Affairs team. 
• Through scientific interactions, you will gain valuable insight into treatment patterns and scientific activities in the field of inflammation and Rheumatology and you will provide strategic input to the company's medical affairs plan.
• Through scientific interactions with external stakeholders, you increase the medical value of our products, based on the risk-benefit profile of our drugs, and contribute to the promotion of innovative therapeutic approaches for patients.

Who are you?

• You have a higher degree in Life Sciences (MD, PharmD, or PhD or equivalent) is required
  
• You have great experience as MSL in the field and more than 3 years of line management experience
  
• You have a solid track record of effective and influential oral presentations within the healthcare / science industry
  
• You have excellent people management skills
• You have proven medical, clinical, or research experience in inflammation and rheumatology
  

What's in it for you?

You become part of a fast growing amazing company. As a “doer” you receive all the support you need to carry out your work successfully. Galapagos strives to recruit the best people who set themselves apart through integrity and excellent interpersonal and organizational skills. Our people are the strength of Galapagos, a highly motivated team dedicated to maintaining the Galapagos leadership position and making breakthroughs in pharmaceutical research. Galapagos offers a competitive compensation package and a dynamic work environment.

We are Galapagos: together we can do it!

About Emerson
At Emerson, we are innovators and problem-solvers, focused on a common purpose: leaving our world in a better place than we found it. Each and every day, our foundational valuesmdash;integrity, safety and quality, supporting our people, customer focus, continuous improvement, collaboration and innovationmdash;inform every decision we make and empower our employees to keep reaching higher.
As a global technology and engineering leader, we provide groundbreaking solutions for customers in industrial, commercial, and residential markets.
Our Automation Solutions business helps process, hybrid, and discrete manufacturers maximize production and protect personnel and the environment while optimizing their energy and operating costs. Our Commercial & Residential Solutions business helps ensure human comfort and health, protect food quality and safety, advance energy efficiency and create sustainable infrastructure.
Emerson, a Fortune 500 company with %2417.4 billion in sales, more than 20 Innovation, Solutions & Engineering Centers, and 200 manufacturing locations worldwide, is committed to helping employees grow and thrive throughout their careers.
Whether you're an established professional looking for a career change, an undergraduate student exploring options or a recent MBA graduate, you'll find a variety of opportunities at Emerson. Join our team and start your journey today.

Would you like to shape the future of a medical technology company dedicated to advancing clinical diagnostics?

Inpeco is the global leader in Total Laboratory Automation. Our game-changing solutions combine open connectivity with full sample traceability to deliver secure test results and increased productivity to clinical laboratories around the world. To date, more than 2000 Inpeco systems have been installed in over 70 countries. Our Group is headquartered in Novazzano, Switzerland, and operates development, manufacturing and sales facilities throughout the world.

The Marketing Communications Specialist increases Inpeco’s global brand awareness and customer loyalty by creating authority-building content and deploying promotional campaigns across multiple channels to connect and continuously engage with customers.

Key responsibilities:

• Fine-tune Inpeco’s brand promise and deploy initiatives to raise brand awareness
• Create and write high quality authority-building content, in collaboration with our in-house experts, customers, business partners and external agencies
• Define and execute content plan (newsletters, press releases, webinars, customer testimonials), both through conventional and digital channels
• Write engaging stories about our business and life at Inpeco
• Deploy promotional campaigns to generate leads, measure results and fine-tune approach
• Produce sales tools (brochures, product videos etc.) in various languages
• Manage Inpeco’s participation at international exhibitions
• Conceptualize international user forums and establish regular dialogue with Inpeco customers
• Lead internal communication to increase employee engagement
• Manage relationships with creative agencies and oversee assigned budget

• Accomplished Marketing Communications Professional with 5+ years of international experience in communication, PR/ marketing, or Digital marketing, preferably in a healthcare related field
• Master’s degree in Communications, PR/ advertising, Journalism, preferably with strong digital marketing experience and a background in Natural Sciences or Healthcare, coupled with an affinity for technology
• Fluency in English is a must (native speakers preferred), other languages are a plus
• Excellent English writing and editing skills (clarity, precision, flow, impact!), combined with creativity and passion for developing authority-building content in a multi-cultural environment
• Experience working with CMS required; experience in graphic design/ DTP is a plus
• Strong project management skills (content planning and managing stakeholders, agencies, budgets, timelines) with track record of on-time delivery
• Creative, curious and proactive personality with customer-centric mindset and power to persuade
• Exemplary team player with integration skills across functions
• Results driven, precise in execution, and with great attention to detail.

Are you ready to join our team of passionate innovators? Then we look forward to receiving your application (CV, motivation letter) in English.

What we offer:

• a dynamic work environment where you can make a difference and grow your career;
• an international work location in our headquarter in Switzerland (Novazzano);
• home office;
• flexible working hours;
• working time account: possibility to accrue additional hours of free time in addition to holidays;
• additional contribution to the pension fund;
• professional and non-professional accident insurance;
• company restaurant for the lunch break;
• car pooling;
• incentives for mobility by public transport;
• agreements for bank account, credit card and personal purchases;
• opportunity of professional and salary growth through various initiatives:

1. annual performance appraisal in order to evaluate the achievement of individual objectives;
2. inner job posting to apply for career opportunities in Inpeco, even between different locations;
3. annual salary review linked to performance and professional development;
4. continuous training on the job, through meetings or conferences, seminars and events

The MSL Team is a part of Medical Affairs and consists of field-based scientists that have direct interactions with investigators and health-care professionals (HCPs) in the field of oncology to provide scientific and medical support regarding the use of tucatinib. As such it requires a strong medical background and excellent communication skills. The (Senior) MSLs work cross-functionally with Clinical Development, Commercial and our internal Medical Affairs colleagues in Italy and region Europe to support our products in close collaboration with our European Medical Affairs team.

Principal Responsibilities:

Be responsible for identifying and building relationships with HCPs, including Key Opinion Leaders (KOLs) within Italy
Deliver scientific presentations internally and externally in either one-on-one or group settings
Facilitate scientific discussions in the field and work with in-house and field partners to facilitate ongoing information/clinical data sharing (e.g. new data, competitive information, customer insights, medical communications support) to optimize communications and coordinated activities across the organization
Compliantly respond to unsolicited HCP requests for off label information. Effectively communicate feedback and insights from the field within Medical Affairs and to other internal partners
Execute conference strategy, including staffing of scientific booths at major conferences and regional clinical meetings in alignment with the companies’ objectives of region Europe
Act as a key liaison for all aspects in the support of investigator sponsored trials (ISTs)
Support planning and execution of local advisory boards
Partner and collaborate effectively with internal business partners, especially with members of the medical and clinical teams in region Europe, to support corporate trials including trial awareness and education
Must stay abreast of relevant medical literature in a self-directed manner
As needed, collaborate with cross-functional partners within Medical Affairs and across other departments
Be a strong individual contributor as well as a valued collaborator on a team.
Take and follow directions, accept guidance from management, and adjust quickly to changes.
Support the achievement of goals while executing all duties in an honest and compliant manner.

Qualifications:

5+ years (10+ years for Senior MSL) of hematology/oncology clinical or basic sciences experience
An advanced doctoral degree (MD, PhD or PharmD) is preferred
Prior MSL experience in oncology preferred
Candidate should have strong presentation / interaction and time management skills and experience in providing evidence based scientific and clinical information to the medical community
Proven ability to establish strong scientific partnerships with key internal and external stakeholders
Working knowledge of applicable country and regional guidelines and regulations.
Prior experience with commercial product launches preferred.
Demonstrate project leadership while recognizing when input from others is needed.
In addition the successful candidate has a track record of:
relating and working with a wide range of people to achieve results
managing time and priorities efficiently and effectively
managing multiple projects in a fast paced environment
50-75% regional travel (by ground and/or air) required. Estimated ≥ 60% time away from remote office, and occasionally on weekends. Must reside within region and live within a reasonable distance of a major airport Thorough understanding of local compliance, as well as a sound ethical approach to business
Fluent in Italian and English
Preferable city location / Region consists of: North-West (Milan centered), North-East, Centre, South

Summary:

With Seagens mission to rapidly bring practice-changing innovations to the oncology landscape and the recent announcement of positive data in HER2+ metastatic breast cancer, we are preparing the launch for tucatinib in Italy and are building the MSL functions.

The MSL Team is a part of Medical Affairs and consists of field-based scientists that have direct interactions with investigators and health-care professionals (HCPs) in the field of oncology to provide scientific and medical support regarding the use of tucatinib. As such it requires a strong medical background and excellent communication skills. The (Senior) MSLs work cross-functionally with Clinical Development, Commercial and our internal Medical Affairs colleagues in Italy and region Europe to support our products in close collaboration with our European Medical Affairs team.

Principal Responsibilities:

Be responsible for identifying and building relationships with HCPs, including Key Opinion Leaders (KOLs) within Italy
Deliver scientific presentations internally and externally in either one-on-one or group settings
Facilitate scientific discussions in the field and work with in-house and field partners to facilitate ongoing information/clinical data sharing (e.g. new data, competitive information, customer insights, medical communications support) to optimize communications and coordinated activities across the organization
Compliantly respond to unsolicited HCP requests for off label information. Effectively communicate feedback and insights from the field within Medical Affairs and to other internal partners
Execute conference strategy, including staffing of scientific booths at major conferences and regional clinical meetings in alignment with the companies’ objectives of region Europe
Act as a key liaison for all aspects in the support of investigator sponsored trials (ISTs)
Support planning and execution of local advisory boards
Partner and collaborate effectively with internal business partners, especially with members of the medical and clinical teams in region Europe, to support corporate trials including trial awareness and education
Must stay abreast of relevant medical literature in a self-directed manner
As needed, collaborate with cross-functional partners within Medical Affairs and across other departments
Be a strong individual contributor as well as a valued collaborator on a team.
Take and follow directions, accept guidance from management, and adjust quickly to changes.
Support the achievement of goals while executing all duties in an honest and compliant manner.
Qualifications:

5+ years (10+ years for Senior MSL) of hematology/oncology clinical or basic sciences experience
An advanced doctoral degree (MD, PhD or PharmD) is preferred
Prior MSL experience in oncology preferred
Candidate should have strong presentation / interaction and time management skills and experience in providing evidence based scientific and clinical information to the medical community
Proven ability to establish strong scientific partnerships with key internal and external stakeholders
Working knowledge of applicable country and regional guidelines and regulations.
Prior experience with commercial product launches preferred.
Demonstrate project leadership while recognizing when input from others is needed.
In addition the successful candidate has a track record of:
relating and working with a wide range of people to achieve results
managing time and priorities efficiently and effectively
managing multiple projects in a fast paced environment
50-75% regional travel (by ground and/or air) required. Estimated ≥ 60% time away from remote office, and occasionally on weekends. Must reside within region and live within a reasonable distance of a major airport Thorough understanding of local compliance, as well as a sound ethical approach to business
Fluent in Italian and English
Preferable city location / Region consists of: North-West (Milan centered), North-East, Centre, South