Employer Industry: Life Sciences and Clinical Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work in a collaborative environment with industry thought leaders and therapeutic experts
- Contribute to meaningful work that positively impacts global health
- Access to resources for achieving individual career goals
- Engaging work in a laboratory setting with a focus on quality and accuracy

What to Expect (Job Responsibilities):
- Assist in the coordination and preparation of scientific documents under direct supervision
- Review technical documents for accuracy, formatting, consistency, and compliance with protocols or SOPs
- Represent the laboratory on project teams and update team members on the status of study reports
- Stay informed on FDA guidelines and requirements for the development of necessary documents
- Collaborate with senior staff on new assignments and perform other duties as assigned

What is Required (Qualifications):
- Bachelor’s degree or equivalent and relevant formal academic/vocational qualification
- Minimum of 2 years of experience providing knowledge, skills, and abilities for the role
- Working knowledge of scientific terminology, medical, pharmaceutical, and research concepts
- Proficiency in word processing, spreadsheets, and table/graph generation
- Effective written and oral communication skills with attention to detail

How to Stand Out (Preferred Qualifications):
- Experience in scientific writing or related fields
- Familiarity with regulatory requirements and documentation processes
- Strong editorial and proofreading skills
- Problem-solving and troubleshooting abilities
- Ability to thrive in a fast-paced, collaborative team environment

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