Jobs Companies AstraZeneca Medical Writing Intern

Sobre este puesto de Medical Writing Intern en AstraZeneca

AstraZeneca · Híbrido · Canada - Mississauga

8-month contract

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Introduction to position:

The primary purpose of this internship will be to provide an opportunity to learn about the role of the medical writer within the pharmaceutical industry and become familiar with the suite of documentation supporting clinical development. The medical writing intern will shadow an experienced writer through the clinical protocol development process and will draft sections of a clinical protocol and/or protocol amendment as assigned by their mentor. The medical writing intern will be accountable for ensuring that deliverables are in line with Alexion’s authoring and QC standards and checklists. This role may support internal medical writing process improvement or template updates.

Specifically, we are seeking individuals with the traits listed below:

  • Motivated self-starter who is results-and process-oriented with a focus on effective and efficient improvements
  • Organized individual with the ability to manage multiple priorities while maintaining high-performance standards
  • Strong writing skills with attention to detail, and comfortable working with a cross-functional and collaborative team

What you will be responsible for:

  • Drafting sections of a clinical protocol and/or protocol amendment or other regulatory documentation as assigned by a mentor.
  • Performing accurate and precise editing and/or proofreading to include spelling, grammar, punctuation, and verification of data in clinical documents (eg, study reports, Investigator's Brochures, protocols, and protocol amendments).
  • Ensuring quality and timeliness of reviewing and editing of clinical documents.
  • Ensuring adherence to Alexion document templates and Style Guide.
  • Attending and participating in Medical Writing and project team meetings.
  • Providing an end of internship summary presentation.

You will need to have:

  • Experience with various MS Office programs, including Word, Outlook, and PowerPoint.
  • The ability to fluently read, write, understand, and communicate in English.
  • Ability to understand clinical, scientific, and statistical data.
  • Good interpersonal, collaborative, and communication skills.
  • Strong attention to detail.
  • Currently enrolled full-time in graduate level scientific or clinical program – Masters, PharmD, PhD, or equivalent. University undergraduate students who have not yet received their BS and are enrolled in a scientific discipline may also be considered.
  • The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer for you to have:

  • Previous experience in writing of clinical or technical documents
  • Experience in clinical research or working with clinical regulatory documents is a plus, but is not required

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 meaningful difference in patients' lives.

Annual base salary for this position ranges from 42,908.00 to 56,316.75.

AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs.  In some cases, offers outside the range may also be considered to address unique circumstances.

In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role).  Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

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Sobre AstraZeneca

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture wh

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