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    • Bachelor’s degree in science (biology, chemistry, microbiology, immunology, medical technology).
    • This role requires a minimum of 40% on-site presence.
    • Bachelor's degree in life sciences or a related field.
    • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
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    • A PhD in a life sciences, health sciences or related research field (biology, psychology, neuroscience, public health or similar), gained through graduate…
    • As a Feasibility Associate, you will support site selection optimization for industry-sponsored clinical research studies across Probity-affiliated sites.
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    • Ability to identify unmet medical, educational, and research needs at the local and regional level in the medical community.
    • PhD, PharmD, MD, or DO required.
    • Staff medical booth at congresses.
    • Deliver medical/scientific trainings (if requested).
    • Doctorate level Degree eg., MD, PhD or PharmD.
    • Participate in executing medical strategy at medical conferences (e.g., staff medical booth, interact with KOLs/HCPs, cover key scientific sessions, internally…
    • Participate in executing the medical strategy at medical conferences (e.g., staff medical booth, interact with KOLs/HCPs, cover key scientific sessions,…
    • Educating the medical community with up-to-date medical and scientific information and exhibiting robust disease expertise and product information.
    • Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.
    • High level of attention to detail and ability to manage/prioritize multiple tasks at a given time.
    • Strong level of interest and knowledge in the cell therapy…
    • Plus de 3 ans d’expérience à titre de MSL (Agent de liaison scientifique médicale).
    • En tant que MSL virtuel(le), vous serez un véritable expert scientifique et…
    • Foster medical and scientific information exchange between the medical community and Sanofi.
    • Assurer la liaison entre les centres académiques et Sanofi.
    • Educating the medical community with up-to-date medical and scientific information and exhibiting robust disease expertise and product information.
    • 2 years experience related to medical pharmaceutical, biotechnology, medical devices industry.
    • Demonstrated experience of developing and presenting scientific/…
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Canadian Blood Services logo
Regulatory Affairs Associate
Ottawa, ON K1G 4J5
•
Hybrid work
$86,400–$101,700 a year
Temporary, Full-time

Job details

Here’s how the job details align with your profile.

Pay

$86,400–$101,700 a year

Job type

Temporary
Full-time

Benefits

Pulled from the full job description
Wellness program

Full job description

This role requires a minimum of 40% on-site presence. Additional on-site work may be required based on business needs. On-site expectations are subject to change and may be adjusted on a temporary or permanent basis.


Job posting ID:
9236


Employment status:
Temporary full-time
Position's anticipated start date: 2026-10-19
Position's anticipated end date: 2028-04-18

Salary/Rate of pay: $86,400 - $101,700


Application deadline:
2026-09-30

  • This external job posting may close earlier than the advertised deadline. We recommend applying as soon as possible.

Application requirements:

  • Your up-to-date resume.
  • Job specific cover letter.
  • We recommend you save a copy of the job posting for reference throughout the recruitment process.


Do you currently work for Canadian Blood Services? All employees must apply via the
internal career page.


Together, the work we do connects people and changes lives — including your own.


Be part of a dynamic, collaborative and caring organization committed to saving and improving lives. Thousands of patients depend on us every day for reliable access to safe blood, plasma, stem cells and organs and tissues.


About the role

Canadian Blood Services is looking for a Temporary Full-time Regulatory Affairs Associate to join our dynamic Quality and Regulatory Affairs team.


The Quality and Regulatory Affairs division is responsible for providing daily support and subject-matter expertise to Canadian Blood Services in regulatory and quality matters, helping the organization to thrive as a biologics manufacturer and provider of transfusion and transplantation services.


In this role, you will integrate and apply your knowledge of domestic and international regulations governing all aspects of Canadian Blood Services’ biological products (fresh blood products, plasma protein products, stem cells, tissues and organs) and services.

Formula for success

  • Leveraging your expertise in compliance management, you will, assist in the development, implementation, and continuous improvement of the national Regulatory Submissions process as it relates to submissions.
  • Harnessing your proficiency in regulatory oversight, you will develop, review, and evaluate regulatory filings for submission to regulatory authorities.
  • Drawing on your acumen in governance and compliance, you will participate in the review of change requests and customer letters submitted by the organization.
  • Leveraging your understanding of industry protocols, you will participate in reviews of industry regulations and standards.
  • Harnessing your mastery of statutory compliance, you will provide interpretation of regulations and standards.
  • Drawing on your aptitude for regulatory navigation, you will assist in the definition, collection, analysis, and review of performance monitoring metrics.

Desired education and skills

  • Bachelor’s degree in science (biology, chemistry, microbiology, immunology, medical technology).
  • Minimum of 2 years’ regulatory experience.
  • Knowledge of domestic and international regulatory requirements, specific to fresh blood components, stem cells, tissues & organs.
  • Thorough understanding of Good Manufacturing Practices.
  • Demonstrated organizational, analytical, problem solving, time management and decision making skills are required.
  • Ability to work on cross-functional teams and the ability to communicate effectively, verbally and in writing, with diverse audiences and personnel.
  • Proficient in writing and editing technical documents.
  • Respect for the sensitivity and confidentiality of documents received and reviewed.

What we offer you

  • Payment in lieu of vacation.
  • Annual performance award up to 6%.
  • Payment in lieu of benefits.
  • Defined benefit pension plan.
  • Employee discounts, wellness program, professional resources.

What you can expect

  • This role will work in a hybrid environment with requirements to be onsite at Canadian Blood Services location 40% of the time.


If this role resonates with you, we encourage you to apply by providing your up-to-date resume. This could be your first step towards a meaningful and inspiring career. Come to work each day knowing that you save lives.


We acknowledge that the work of Canadian Blood Services spans many Territories and Treaty areas across the country, and we are grateful for the Traditional Knowledge Keepers and Elders who have guided us in this important work. We recognize the land and waters that have inspired our work and offer gratitude to those Indigenous peoples on whose territory we work, live and play.


Diversity and inclusion play a vital role in ensuring health equity for patients across Canada. We are committed to reflecting Canada’s population in our organization and fostering an environment where all employees can be their authentic selves, with equal opportunities to succeed and contribute.


We thank all applicants for their interest. However, only those considered for an interview or those invited to participate in an assessment will be contacted. Emails are sent directly from our system, to ensure you receive them please add donotreply@blood.ca and system@successfactors.com to your safe senders list.


Applicants who require accommodation should discuss their needs with us.

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