Employer Industry: Pharmaceutical Industry

Why consider this job opportunity:
- Salary up to $134,800
- Bonus eligibility and long-term incentives available
- Comprehensive health care and insurance benefits for employees and their families
- Retirement benefits with paid holidays, vacation, and sick days
- Opportunity for career advancement and growth within the organization
- Flexible hybrid work model, with three days on-site and the option to work remotely on Fridays

What to Expect (Job Responsibilities):
- Review and prepare documents to ensure personal protected information is removed
- Facilitate collaborative reviews with contributing authors and product development teams to identify commercially confidential information
- Execute quality checks of documents and complete associated justifications
- Manage disclosure timelines and participate in submission planning management team meetings
- Monitor and escalate potential incidents regarding the release of protected information

What is Required (Qualifications):
- Bachelor’s degree in Life Sciences or a related discipline
- 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 the content of drug and/or device study submission documents
- Knowledgeable in European Medicines Agency's (EMA) and/or Health Canada publication requirements for clinical information

How to Stand Out (Preferred Qualifications):
- Highly organized, capable of managing 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
- Capacity to work independently and collaboratively in a team environment

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We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."