Intern, Clinical Regulatory Writing
Full TimeRemoteTeam 1,001-5,000
Location
United States
Posted
9 hours ago
Salary
Not specified
No structured requirement data.
Job Description
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Role Description
This is a unique opportunity for either master's or PhD students to support the clinical regulatory writing team in the clinical development of treatments for rare and ultra-rare diseases. The clinical regulatory writing intern will work closely with the medical writing and cross-functional teams to develop high quality clinical and regulatory documents for global marketing applications.
- Participate in the authoring and review of clinical and regulatory documents relating to global marketing applications and clinical trials (e.g., clinical study reports, protocols, safety narratives)
- Learn and apply medical writing standards
- Understand the process of distilling large amounts of clinical and scientific data into essential elements for tabular and graphical display
- Perform literature-based research to support writing activities
- Begin to understand global and regional regulatory requirements (e.g., ICH E3) and how they impact clinical and regulatory writing
- Liaise with clinical trial transparency colleagues to understand how data from clinical and regulatory documents is disclosed publicly
Qualifications
- Pursuing a Master’s degree or PhD in a scientific or medical field with a minimum of first year completed
- Understanding of basic biology, clinical research, and medical terminology
- Enrolled as a full-time student
- Able to work 40 hours/week during normal business hours
- Proficient with Microsoft Office Suite
- Knowledgeable regarding the use of AI tools
- Detail oriented, strong organizational skills
- Flexible; adapts work style to meet organizational needs
- Good verbal and written communication skills; ability to write clearly and effectively
- Capable of completing assigned responsibilities within timelines and providing their manager with project status updates
Requirements
- U.S. Hourly Wage Range: $30.00-$40.00 per hour
- The actual hourly wage offered will depend on the candidate’s school year/level
Benefits
- Generous vacation time and public holidays observed by the company
- Volunteer days
- Long term incentive and Employee stock purchase plans or equivalent offerings
- Employee wellbeing benefits
- Fitness reimbursement
- Tuition sponsoring
- Professional development plans
- Benefits vary by region and country
Job Requirements
- Pursuing a Master’s degree or PhD in a scientific or medical field with a minimum of first year completed
- Understanding of basic biology, clinical research, and medical terminology
- Enrolled as a full-time student
- Able to work 40 hours/week during normal business hours
- Proficient with Microsoft Office Suite
- Knowledgeable regarding the use of AI tools
- Detail oriented, strong organizational skills
- Flexible; adapts work style to meet organizational needs
- Good verbal and written communication skills; ability to write clearly and effectively
- Capable of completing assigned responsibilities within timelines and providing their manager with project status updates
- U.S. Hourly Wage Range: $30.00-$40.00 per hour
- The actual hourly wage offered will depend on the candidate’s school year/level
Benefits
- Generous vacation time and public holidays observed by the company
- Volunteer days
- Long term incentive and Employee stock purchase plans or equivalent offerings
- Employee wellbeing benefits
- Fitness reimbursement
- Tuition sponsoring
- Professional development plans
- Benefits vary by region and country