Senior Medical Writer shaping key clinical and regulatory documents at Thermo Fisher Scientific. Collaborating with teams to drive strategy, quality, and execution of early - phase programs.
About the role
- Analyst/Medical Writer conducting detailed data analysis from clinical trials at Costello Medical. Engaging collaboratively on various projects while developing strong scientific and writing skills in healthcare communications.
Responsibilities
- Conducting detailed analysis of clinical trial data and creating materials for different audiences
- Close collaboration with clients, including participating in teleconferences and face-to-face meetings
- Supporting project management and client communication alongside experienced colleagues
- Working on several projects in different disease areas simultaneously
- Engaging with different teams within the company
Requirements
- An undergraduate degree level qualification in a scientific discipline (minimum 2.1 or equivalent)
- An aptitude for, and experience of, planning and writing scientific documents
- A self-motivated and enthusiastic approach, with a genuine interest in healthcare
- An exceptional level of attention to detail
- Strong analytical skills
- Excellent organisational skills
- Exceptional written English
- Effective verbal communication skills
- The ability to tailor your communication style to a variety of audiences
- A proactive mindset
- A collaborative approach to working
- The self-awareness to reflect on your own work and performance
- A willingness to get involved with, and contribute to, your wider team
- Fluency in Microsoft Word, Excel and PowerPoint
Benefits
- Discretionary profit share bonuses paid twice per year
- Hybrid and flexible working options
- Generous holiday allowance
- Private medical insurance
- Critical illness cover
- Income protection
- Full funding for external training
- Paid study leave and funding for external qualifications
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