Analyst/Medical Writer

Role Summary The Analyst and Medical Writer positions are ideal for recent graduates in the sciences, and those with experience in scientific research, who are seeking the opportunity to apply their knowledge to real-world projects. Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats including posters, slide sets, value dossiers, reports and peer‑reviewed publications. These deliverables are used directly by our clients in communication with external stakeholders, which are instrumental to the successful uptake of novel therapies. The work is structured on a project‑by‑project basis and you will be working on three or four projects at any one time across a range of high‑profile disease areas and products, presenting variety of work and the opportunity to develop a wide skill set. You will work in project teams alongside experienced colleagues who will provide training on the technical aspects of the role as well as project management and effective client communication. Delivering project work requires close collaboration with clients, and following a successful induction period you will increasingly participate in teleconferences and face‑to‑face client meetings. The latter may present opportunities for travel within the US and internationally. Key Responsibilities Work on projects that involve the detailed analysis and presentation of clinical data, which are instrumental to the successful uptake of novel therapies. Collaborate closely with clients and cross‑functional teams to produce deliverables such as posters, slide sets, value dossiers, reports, manuscripts, and regulatory documents. Participate in project planning, evidence synthesis, data interpretation, and the development of clear and creative written content for a variety of audiences. Manage multiple projects simultaneously, ensuring on‑time delivery and high‑quality standards while representing the company in client interactions. Travel may be required for client meetings, conferences, and on‑site support at medical education events. Qualifications A bachelor’s degree in a scientific discipline (minimum GPA 3.3). We welcome applications from candidates with a diverse range of educational backgrounds, but particularly those with coursework in the life sciences. An excellent written and spoken fluency in English. An ability to communicate scientific materials clearly in both written and oral form. An excellent understanding of and ability to apply scientific concepts. A close attention to detail. An aptitude for and experience with scientific writing which could include dissertations, research summaries, lab reports, poster or oral presentations, peer‑reviewed scientific publications, book chapters, literature reviews, grant applications, regulatory documents, and articles for websites or student magazines. A competency in Microsoft Word, Excel and PowerPoint. An exceptional level of organizational skills and the ability to effectively manage your time and meet deadlines. No previous experience in this sector is necessary, but you should display a genuine interest in healthcare and an eagerness to learn about new areas of clinical science. Applicants with higher‑level qualifications in a scientific discipline are welcomed but this is not a requirement. Benefits A starting salary of $70,000 per annum. This increases to $72,000 for successful candidates who hold a master’s qualification and $73,000 for those with a PhD. Please note that this salary is standardized and non‑negotiable. Private medical insurance with a company contribution. Dental and vision cover. 23 days’ vacation leave increasing by 1 day to a maximum of 27 days. 6 public holidays plus 1 floating holiday. The chance to work from home for up to half of your working time. Retirement savings via a 401(k) plan with up to a 5% employer match. Paid funding for external education and study leave. Life insurance. Comprehensive travel insurance. Flexible and reasonable working hours. Regular company‑funded social activities. Location & Start Date Boston office. We are currently recruiting for start dates throughout 2025. Equal Opportunity Statement As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Visa Sponsorship We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa. #J-18808-Ljbffr