Job Description

Company Description
Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development. We have nourished a true international culture here at Ergomed. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives.


Due to continued growth we are seeking a Senior Medical Writer. The Medical Writer is responsible for the content, quality, and timely delivery of technical documents in support of clinical study activities. As a Senior Medical Writer you will be responsible for (but not limited to) the following activities:

• Maintains responsibility for all assigned duties within a clinical study, this may include - ensuring that work is performed on time, communicating issues and updates to the study lead in a timely manner; and ensuring all content created/reviewed is appropriate, valid, and relevant to the study and of high quality.
• Contributing to the quality, structure, and content for technical documentation within assigned clinical studies
• Act as the study lead for multiple studies, clinical programs, and/or large/complex studies with responsibility for all medical writing related activities
• Able to function independently for nearly all activities; only requiring support for novel, complex, or otherwise atypical activities,
• Provide review and oversight to technical documents created by other members of the medical writing department,
• Able to review technical and scientific documentation for unfamiliar topics to develop technical content, summarize findings, ensure scientific validity, and statement of ethical issues

Qualifications

• Previous experience of pharmacovigilance medical writing, including PBRERs, DSURs, RMPs writing
• Life Science degree, or have equivalent nursing or medical qualifications
• Ability to manage multiple and varied tasks and prioritize workload with attention to detail
• Ability to effectively train and mentor Associate Medical Writers
• Advanced knowledge of English

Additional Information
Why Ergomed We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer:

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues based all over the world, with English as the company language

Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join! Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships We look forward to welcoming your application.