Employer Industry: Pharmaceutical Industry

Why consider this job opportunity:
- Salary up to $134,800
- Bonus eligibility and long-term incentive benefits available
- Comprehensive healthcare and insurance benefits for employees and their families
- Generous retirement benefits, paid holidays, vacation, and sick days
- Opportunity for career advancement and growth within the organization
- Flexible hybrid work model with remote work options

What to Expect (Job Responsibilities):
- Review and prepare documents to ensure personal protected information is removed
- Facilitate collaborative reviews with authors and product development teams to identify commercially confidential information
- Execute quality checks on documents and complete associated justifications
- Manage disclosure timelines and participate in submission planning meetings
- Provide input and feedback on Standard Operating Procedures for public document preparation

What is Required (Qualifications):
- Bachelor's degree in Life Sciences or a related discipline
- Minimum of three (3) years of pharmaceutical industry and/or clinical research experience
- Proficiency in using a Doc base system or similar Electronic Document Management system
- Experience writing or understanding content of drug and/or device study submission documents
- Knowledge of European Medicines Agency's (EMA) and/or Health Canada publication requirements for clinical information

How to Stand Out (Preferred Qualifications):
- Highly organized with the ability to manage multiple projects simultaneously
- Strong attention to detail and commitment to excellence
- Ability to work under pressure while maintaining a positive attitude
- Excellent communication and stakeholder management skills
- Capability to work independently and collaboratively in a team environment

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