Analyst/Medical Writer responsible for analyzing clinical trial data and creating communications materials. Engaging with clients and producing abstracts, manuscripts, and presentations for external stakeholders.
Responsibilities
Work on medical communications projects involving detailed analysis and presentation of clinical trial data
Collaborate with clients and provide materials for various audiences
Conduct analysis of clinical trial data
Engage in teleconferences and face-to-face meetings with stakeholders
Support project management alongside experienced colleagues
Participate in the creation of abstracts, manuscripts, posters, and oral presentations
Work across multiple projects in different disease areas
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
A willingness to get involved with, and contribute to, your wider team
Embodying Costello Medical’s values
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
Holiday buy and sell scheme
Paid study leave and funding for external qualifications
Paid and unpaid sabbaticals based on length of service
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.
Medical Writer I ensuring data integrity and quality checks for clinical documents in a biopharmaceutical company. Collaborating with medical writing teams and participating in stakeholder meetings.
Medical Writer creating impactful documentation for clinical studies and regulatory submissions. Collaborating with internal teams and ensuring clarity and compliance in scientific communications.
Lead Medical Writer responsible for clinical study documents at Fortrea. Collaborating with writers and ensuring high - quality delivery for various studies.
Clinical Documentation Improvement Specialist educating clinicians on documentation and coding requirements. Collaborating across healthcare facilities and providing training to improve documentation quality.
Clinical Analyst managing electronic health record processes and supporting patient order workflows in healthcare. Ensuring data accuracy and compliance while assisting with referrals and clinical documentation.
Senior Medical Writer executing medical communication and consultancy projects at Decera Clinical. Serving as key scientific contact and mentor while supporting business development efforts.
Auditor - CDI Nurse Educator for clinical documentation improvement at Northeast Georgia Health System. Conducting audits, training staff and ensuring accurate clinical data reporting.
Senior Analyst leading medical communications projects for Costello Medical, managing client deliverables and project teams effectively while ensuring high - quality work standards.
Clinical Documentation Specialist role at Advocate Health facilitating documentation modifications and educating teams. Supporting accurate clinical documentation through chart reviews and interactions with healthcare professionals.