Country Operations Management Intern
Top Benefits
About the role
Join Alexion, a leader in rare disease biopharma, where innovation meets dedication. Since 2009, we've been transforming lives in Canada with groundbreaking medicines for rare diseases. Our legacy is built on scientific expertise and patient-centric decision-making, driving us to push the boundaries of science and deliver transformative medicines.
At Alexion, we are dedicated to providing unwavering commitment and investment in therapies that help patients live longer, fuller lives. With over 200 employees in Canada, our global research and development hub is driven by highly skilled professionals conducting clinical trials locally and globally. Our passionate teams ensure that our treatments reach those who need them most. Join us in driving patient impact both locally and globally!
Introduction To Role The Intern, Country Operations Management (ICOM) is a working student that joins the COM team to be trained and learn about the Clinical Research and pharmaceutical industry field while providing support to their colleagues, as needed.
The ICOM is accountable within their region (cluster) for supporting the COM team in the successful execution of study deliverables and the quality execution of high priority and / or complex protocol procedures through adherence to good clinical practices (GCP),evolving regulatory requirements, and ensuring quality and consistency in timely completion of study activities.
Responsibilities/Accountabilities Accountable For:
- Support the COM team in achieving quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation)
- Support the COM team in reporting of study-specific issues (including monitoring metrics) to the study team
- May support the CDA delivery and negotiation (based on pre-approved parameters and regardless of executory party).
- May support in the negotiation of site study contracts and budgets for the studies at country level as requested by COM team.
- May support in review of local regulatory documentation and local regulatory activities.
- Provide support in remote and onsite monitoring activities for assigned studies
- Provide support in coordination of country level engagement activities.
- Provide support country calls with local study team and/or CRO, as applicable.
- Lead process improvement initiatives that supports the cluster goals
Responsible For
- Support Meeting preparation (agendas, materials, … )
- Support Filing activities
- Provide other Administrative support to projects
- Ad hoc support study teams in site management during start up phase including but not limited to contract negotiation, EC/CA submissions matters, site initiation visits preparation administrative tasks and recruitment phase of the study.
- Ad hoc support of Clinical Monitoring activities, from documentation review (reports, metrics, etc) to onsite support (site documentation management, IP accountability support, SDR/SDR support to CRA, ….) for the assigned studies and communicate monitoring deficiencies to SML as applicable.
- Support SMLs in monitoring oversight tools maintenance.
- Timely and accurate responses to queries from the country team.
- May participate in meetings Medical Affairs to coordinate site feasibility.
- Support Inspection readiness activities at local level for assigned studies.
- Support the development and maintenance of project management tracking tools (e.g: CTMS, smartsheets, etc).
Qualifications
- Currently enrolled in a post-secondary program
- Currently studying in one of the disciplines related to clinical practice/health care, life sciences or drug development is required. A clinical or advanced degree (RN, MPH, MS, MA, MBA, PharmD,) is preferred.
- Good organizational skills and ability to deal with competing priorities.
- Effective communication skills (written, verbal and presentation).
- Creative thinker, curious and unafraid to ask questions.
- Innovator, willing to initiate changes, introduce new ideas, and creatively problem solve.
- Proficient with MS Office Suite (Excel, Word and PowerPoint).
- Available to work from January 2026 to December 2026.
What You’ll Learn As an Intern at Alexion Canada, AstraZeneca Rare Disease, you will have the opportunity to learn about various positions with Alexion as you work cross-functionally with different parts of our business. Our purpose for this position is to ensure you gain key foundational knowledge that will complement your education through interesting work while leveraging valuable networking opportunities to expand your learning.
What To Expect This role is a 12-month paid contract position, which starts in January 2026 and will end in December 2026. Our position will be based in our Mississauga head office and allow for flexible working arrangements working both onsite (3 times per week) and virtually.
At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a substantial difference in patients' lives.
Joining Alexion means embracing an opportunity where work isn't ordinary. Our closeness to patients brings us closer to our work and each other. With a groundbreaking spirit, we are outstanding in R&D and healthcare. Grow and innovate in a rapidly expanding portfolio while enjoying the entrepreneurial spirit of a leading biotech. You'll be empowered with tailored development programs crafted for skill enhancement and encouraging a deep understanding of our patients' journeys. Supported by outstanding leaders and peers, you'll inspire change with integrity in a culture that celebrates diversity, innovation, and connection to patients' lived experiences.
Ready to embark on this journey? Apply now to join our team!
Date Posted 27-Oct-2025
Closing Date 02-Nov-2025
Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify.
About Alexion Pharmaceuticals, Inc.
Alexion, AstraZeneca Rare Disease was created following the 2021 acquisition of Alexion Pharmaceuticals, Inc. by AstraZeneca. For more than 30 years, Alexion’s mission has been to transform the lives of people affected by rare diseases through the development and delivery of innovative medicines, supportive technologies, and healthcare services. Dedicated to continuing its mission as part of AstraZeneca, Alexion recognizes that patients and caregivers are people first, and by understanding their experiences, Alexion is better able to serve their unique needs.
Alexion’s pioneering legacy in rare disease is rooted in being the first to translate the complex biology of the complement system into novel medicines. Alexion pushes boundaries to accelerate discovery of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the world and continues to expand its reach to benefit more people globally.
GL/NP/0116 GL/NP/0095
Community Guidelines: https://bit.ly/39x9gqy
Country Operations Management Intern
Top Benefits
About the role
Join Alexion, a leader in rare disease biopharma, where innovation meets dedication. Since 2009, we've been transforming lives in Canada with groundbreaking medicines for rare diseases. Our legacy is built on scientific expertise and patient-centric decision-making, driving us to push the boundaries of science and deliver transformative medicines.
At Alexion, we are dedicated to providing unwavering commitment and investment in therapies that help patients live longer, fuller lives. With over 200 employees in Canada, our global research and development hub is driven by highly skilled professionals conducting clinical trials locally and globally. Our passionate teams ensure that our treatments reach those who need them most. Join us in driving patient impact both locally and globally!
Introduction To Role The Intern, Country Operations Management (ICOM) is a working student that joins the COM team to be trained and learn about the Clinical Research and pharmaceutical industry field while providing support to their colleagues, as needed.
The ICOM is accountable within their region (cluster) for supporting the COM team in the successful execution of study deliverables and the quality execution of high priority and / or complex protocol procedures through adherence to good clinical practices (GCP),evolving regulatory requirements, and ensuring quality and consistency in timely completion of study activities.
Responsibilities/Accountabilities Accountable For:
- Support the COM team in achieving quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation)
- Support the COM team in reporting of study-specific issues (including monitoring metrics) to the study team
- May support the CDA delivery and negotiation (based on pre-approved parameters and regardless of executory party).
- May support in the negotiation of site study contracts and budgets for the studies at country level as requested by COM team.
- May support in review of local regulatory documentation and local regulatory activities.
- Provide support in remote and onsite monitoring activities for assigned studies
- Provide support in coordination of country level engagement activities.
- Provide support country calls with local study team and/or CRO, as applicable.
- Lead process improvement initiatives that supports the cluster goals
Responsible For
- Support Meeting preparation (agendas, materials, … )
- Support Filing activities
- Provide other Administrative support to projects
- Ad hoc support study teams in site management during start up phase including but not limited to contract negotiation, EC/CA submissions matters, site initiation visits preparation administrative tasks and recruitment phase of the study.
- Ad hoc support of Clinical Monitoring activities, from documentation review (reports, metrics, etc) to onsite support (site documentation management, IP accountability support, SDR/SDR support to CRA, ….) for the assigned studies and communicate monitoring deficiencies to SML as applicable.
- Support SMLs in monitoring oversight tools maintenance.
- Timely and accurate responses to queries from the country team.
- May participate in meetings Medical Affairs to coordinate site feasibility.
- Support Inspection readiness activities at local level for assigned studies.
- Support the development and maintenance of project management tracking tools (e.g: CTMS, smartsheets, etc).
Qualifications
- Currently enrolled in a post-secondary program
- Currently studying in one of the disciplines related to clinical practice/health care, life sciences or drug development is required. A clinical or advanced degree (RN, MPH, MS, MA, MBA, PharmD,) is preferred.
- Good organizational skills and ability to deal with competing priorities.
- Effective communication skills (written, verbal and presentation).
- Creative thinker, curious and unafraid to ask questions.
- Innovator, willing to initiate changes, introduce new ideas, and creatively problem solve.
- Proficient with MS Office Suite (Excel, Word and PowerPoint).
- Available to work from January 2026 to December 2026.
What You’ll Learn As an Intern at Alexion Canada, AstraZeneca Rare Disease, you will have the opportunity to learn about various positions with Alexion as you work cross-functionally with different parts of our business. Our purpose for this position is to ensure you gain key foundational knowledge that will complement your education through interesting work while leveraging valuable networking opportunities to expand your learning.
What To Expect This role is a 12-month paid contract position, which starts in January 2026 and will end in December 2026. Our position will be based in our Mississauga head office and allow for flexible working arrangements working both onsite (3 times per week) and virtually.
At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a substantial difference in patients' lives.
Joining Alexion means embracing an opportunity where work isn't ordinary. Our closeness to patients brings us closer to our work and each other. With a groundbreaking spirit, we are outstanding in R&D and healthcare. Grow and innovate in a rapidly expanding portfolio while enjoying the entrepreneurial spirit of a leading biotech. You'll be empowered with tailored development programs crafted for skill enhancement and encouraging a deep understanding of our patients' journeys. Supported by outstanding leaders and peers, you'll inspire change with integrity in a culture that celebrates diversity, innovation, and connection to patients' lived experiences.
Ready to embark on this journey? Apply now to join our team!
Date Posted 27-Oct-2025
Closing Date 02-Nov-2025
Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify.
About Alexion Pharmaceuticals, Inc.
Alexion, AstraZeneca Rare Disease was created following the 2021 acquisition of Alexion Pharmaceuticals, Inc. by AstraZeneca. For more than 30 years, Alexion’s mission has been to transform the lives of people affected by rare diseases through the development and delivery of innovative medicines, supportive technologies, and healthcare services. Dedicated to continuing its mission as part of AstraZeneca, Alexion recognizes that patients and caregivers are people first, and by understanding their experiences, Alexion is better able to serve their unique needs.
Alexion’s pioneering legacy in rare disease is rooted in being the first to translate the complex biology of the complement system into novel medicines. Alexion pushes boundaries to accelerate discovery of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the world and continues to expand its reach to benefit more people globally.
GL/NP/0116 GL/NP/0095
Community Guidelines: https://bit.ly/39x9gqy