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Indegene: Medical Information Manager (Canada)

Role overview

Qualifications

  • Experience in medical information function, including knowledge of regulations/guidelines and operations
  • Strong oral and written communication skills
  • Ability to work in team environment and collaborate with global medical information and cross-functional business partners
  • PharmD, PhD, or MD

Responsibilities

  • Delivers high-quality, balanced and timely written or verbal medical and scientific information upon the request of health care professionals and consumers
  • Researches appropriate sources of data/information to provide quick, accurate and thorough responses
  • Contributes to the development and maintenance of standard and custom medical information responses in various formats
  • Maintains up-to-date medical information and knowledge management systems/repositories

Key facts

Hard skills

Other skills

  • Communication
  • Collaboration
  • Teamwork
  • Problem Solving

About the company

Trilogy Writing & Consulting logo

Trilogy Writing & Consulting

Research & Scientific Services

At Trilogy, medical writing is our passion. As specialists in clinical regulatory documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams: proactively planning, coordinating and writing their clinical documents to meet timelines, with a readability that reduces the time for review and approval. We have been helping pharmaceutical companies and clinical research organizations of all sizes, worldwide, to streamline their documentation processes for over 18 years – either as support on a one-off document or the entire clinical development program. We provide our clients with a constructive advice on their projects: we guide our clients’ teams through the writing process and ask them the right questions in order to produce documents that communicate effectively. Our writers are trained to understand that our job is not to produce a data dump: it is to think about the data available and work with the team to pull out the messages and present them as clearly as possible, so that a reviewer can quickly find the information they are looking for and easily understand the story to be told. Our approach to writing clinical documentation ideally results in a minimum of clarifying questions from reviewers, speeding the process of review and ultimately leading to faster approval. Trilogy currently has more than 50 writers, who are located in Trilogy’s 3 offices: Frankfurt in Germany (HQ), Cambridge in the UK, and Durham, North Carolina in the US.

Company details

Company typeSME
IndustryResearch & Scientific Services
Company size51 - 200

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Job description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. 

What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it? We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams and be responsible for the outcomes while our leaders support and mentor you.

We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you.

Medical Information Manager (must be based in Canada)


You will be responsible for:

  • Delivers high-quality, balanced and timely written or verbal medical and scientific information upon the request of health care professionals and consumers.
  • Researches the appropriate sources of data / information to provide a quick, accurate and thorough response.
  • Contributes to the development (research, outline, compose, review) and maintenance of standard and custom medical information responses in various formats to address vast array of inquiries.
  • Liaises with third party contact center as it relates to Compliance with workflow procedures and standards
    • Inquiries requiring escalation or customization
    • Corrections resulting from quality control / case review activities
    • New hire or ongoing therapeutic area/product training, as applicable
  • Supports the generation of therapeutic area metrics and analytics; maintains in-depth understanding of historic trends and insights of inquiries received.
  • Maintains up-to-date medical information and knowledge management systems / repositories
  • Understands and effectively applies and complies with appropriate ethical, legal and regulatory standards, including those for responding to unsolicited requests for information, on / off label inquiries, and product promotion.
  • As applicable, reports any product quality complaints and adverse events to Quality Assurance / Drug Safety per corporate policies.

Your impact:

The Global Medical Information Manager will sustain and promote company’s professional standing and integrity amongst patients, health care professionals and the pharmaceutical / biotech industry by delivering high quality responses to unsolicited requests for information. The Specialist is responsible for providing accurate, timely, balanced and up-to-date medical and scientific information to internal and external customers, globally. This role is responsible for developing and maintaining current, broad, and in-depth knowledge of pathophysiology, pharmacotherapy, and patient outcomes associated with assigned Alexion products and disease states.

The employee carries out this role in accordance with departmental SOPs, corporate policy and other legal and regulatory requirements.

Must have:

Qualifications

  • Experience in medical information function, including knowledge of regulations / guidelines and operations
  • Strong oral and written communication skills
  • Ability to work in team environment and collaborate with global medical information and cross-functional business partners
  • Excellent people and project management skills
  • Knowledge of IRMS medical information database (preferred)
  • Experience with writing medical information content such as standard response letters
  • Experience in managing others within medical information department

Education

  • PharmD, PhD, or MD

 Compensation: $140,000 - $150,000CAD

EQUAL OPPORTUNITY

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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