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Internship Global Patient Safety Jobs (NOW HIRING)

Title: VIE - Global Patient Safety Americas Company: Ipsen Innovation (SAS) About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three ...

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Internship Global Patient Safety information

What is an internship in global patient safety?

An Internship in Global Patient Safety is a temporary position for students or recent graduates to gain experience in the field of patient safety within a global healthcare or pharmaceutical organization. Interns typically work with teams to analyze safety data, assist in risk management, and help ensure that products and processes meet regulatory and ethical standards for patient care. The role provides valuable exposure to pharmacovigilance, regulatory affairs, and the broader landscape of drug safety. It is ideal for those interested in healthcare, public health, or life sciences. Interns often have opportunities to learn from experienced professionals and contribute to real-world projects that impact patient well-being worldwide.

What types of projects and responsibilities can I expect during an internship in global patient safety?

As an intern in Global Patient Safety, you will typically support the monitoring and analysis of adverse event reports, assist in risk management activities, and help prepare safety documentation for regulatory submissions. You may also collaborate with cross-functional teams such as clinical development, regulatory affairs, and medical affairs. Interns often gain hands-on experience with pharmacovigilance databases and participate in team meetings, providing valuable insight into post-market safety surveillance and compliance processes. This role offers exposure to real-world safety cases and contributes directly to the safe use of pharmaceutical products.

What are the key skills and qualifications needed to thrive as an internship in global patient safety, and why are they important?

To thrive as an Internship Global Patient Safety, you need a background in life sciences or pharmacy, strong analytical abilities, and attention to detail, often supported by progress toward a relevant degree. Familiarity with pharmacovigilance databases, safety reporting systems like MedDRA and Argus, and Microsoft Office tools is typically required. Excellent communication, teamwork, and organizational skills help interns effectively collaborate and manage diverse safety data. These skills are crucial to ensure accurate monitoring, assessment, and reporting of drug safety information, ultimately protecting patient health.

What is the difference between Internship Global Patient Safety vs Internship Pharmacovigilance?

AspectInternship Global Patient SafetyInternship Pharmacovigilance
Required CredentialsUndergraduate or graduate degree in life sciences, healthcare, or related fieldsSimilar educational background, often with focus on pharmacology or pharmacy
Work EnvironmentPharmaceutical companies, healthcare organizations, clinical research settingsPharmaceutical companies, regulatory agencies, clinical research organizations
Industry UsageFocuses on patient safety, adverse event monitoring, and risk managementFocuses on drug safety, adverse event reporting, and regulatory compliance

Both internships involve monitoring drug safety and require similar educational backgrounds. However, Global Patient Safety emphasizes patient-centered safety initiatives and risk management, while Pharmacovigilance focuses more on adverse event reporting and regulatory compliance related to drug safety.

What cities are hiring for Internship Global Patient Safety jobs?

Cities with the most Internship Global Patient Safety job openings:

What are the most commonly searched types of Global Patient Safety jobs?

The most popular types of Global Patient Safety jobs are:

What states have the most Internship Global Patient Safety jobs?

States with the most job openings for Internship Global Patient Safety jobs include:

VIE - Global Patient Safety Americas

Ipsen

Boston, MA • On-site

Full-time

Re-posted 27 days ago


Key responsibilities

  • Support oversight of Pharmacovigilance activities across the Americas region.

  • Partner with Ipsen affiliates and external partners to ensure compliance with global PV requirements and local regulations.

  • Review monthly Pharmacovigilance reports and support compliance monitoring activities.


Job description

Title:

VIE - Global Patient Safety Americas

Company:

Ipsen Innovation (SAS)


About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company's success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/and follow our latest news on LinkedIn and Instagram.

Job Description:

V.I.E (Volontariat International en Entreprise) is a program run by Business France, the French government agency. It allows young professionals from the European Economic Area to work for a French company outside of France for a limited period. Participants are not Ipsen employees but have a special V.I.E status.

To take part in the program, there are specific eligibility criteria that must be met and will be verified by Business France. Those who do not meet the eligibility criteria cannot be part of this program but can apply to other opportunities within Ipsen.

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Join Ipsen's Global Patient Safety team and support Pharmacovigilance activities across the Americas. Working closely with affiliates and commercial partners, you will help ensure compliance with global PV requirements while contributing to patient safety worldwide.

Location: Boston, MA, USA

Department: Global Patient Safety (GPS)
Duration: 18months VIE Contract

Your Key Responsibilities

  • Support oversight of Pharmacovigilance activities across the Americas region.

  • Partner with Ipsen affiliates and external partners to ensure compliance with global PV requirements and local regulations.

  • Coordinate follow-up actions arising from regional governance meetings.

  • Review monthly Pharmacovigilance reports and support compliance monitoring activities.

  • Assist with Patient Data Collection Systems (PDCS) and Digital Media PV compliance reviews.

  • Support audit preparation, quality initiatives, and implementation of global PV processes.

  • Collaborate with global and regional stakeholders in a dynamic international environment.

About You

  • Master's degree in Life Sciences, Pharmacy, or a related discipline.

  • Strong interest in Pharmacovigilance, Drug Safety, or the pharmaceutical industry. Knowledge of Good Pharmacovigilance Practices (GVP) is a plus.

  • Fluent in English.

  • Organized, proactive, and able to manage multiple priorities.

  • Strong communication and stakeholder management skills.

  • Comfortable working in a global, matrix environment.

Why Ipsen?

This VIE assignment offers a unique opportunity to gain international exposure, develop expertise in Pharmacovigilance, and make a meaningful contribution to patient safety while working with teams across the Americas.

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace "The Real Us". The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application. Ipsen is an equal opportunity employer that strictly prohibits unlawful discrimination. We recruit, employ, train, compensate, and promote without regard to an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.