UK ~ Edinburgh
Trainee Medical Writing Coordinator
Our growing and successful business comprises of over 700 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.
People join Quotient Sciences because we are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.
This is an excellent opportunity to start your career as a Medical Writing Coordinator within the challenging environment of early phase clinical studies and be trained in the many different aspects of medical writing and clinical data.
The Data Sciences group at Quotient Sciences comprises over 60 staff and provides an expert service in the data management, analysis and report writing of early Phase clinical studies (both healthy volunteer and patient). Due to our continued growth and success we have an excellent opportunity for a talented trainee Medical Writing Coordinator to join our Medical Writing department and further your career. Other project team members will perform tasks such as study database set-up, collection of data, statistical analysis, etc. Working as part of the project team, your role will be to:
- Assist the Medical Writing staff by performing QC tasks and providing administrative support in the generation of documents such as Clinical Study Protocols and Clinical Study Reports
- Collate appendices and publish Clinical Study Reports
- Provide general administrative support to the wider Data Sciences group
The role of a Medical Writer Coordinator is a key one within the Quotient project team; it involves working closely with other staff in our Medical Writing department and when required, also our statisticians, programmers and project managers. We use our own document templates/procedures or sponsor templates/procedures as required; full training will be provided in these and medical writing coordination techniques. Dependent on your development, our career pathway allows you to expand your skills over time and progress to more senior roles and tasks.
The successful candidate will have good Microsoft Word skills, some form of scientific background (eg prior experience working for a company in a research environment, scientific qualifications, etc) and an interest in a career as a Medical Writing Coordinator. Some prior experience of clinical trials (eg as a CTA or similar clinical support role), administrative support for pre-clinical report writing (eg toxicology reports) or knowledge of GCP or GLP would be an advantage. Candidates with previous medical writing coordination experience will be considered for a more senior role.
In addition you should have good organizational and communication skills and be able to work to deadlines whilst maintaining quality standards. Attention to detail and the ability to multitask are essential. Applicants must have the right to work in the UK upon being offered employment.
The role will be based in our Edinburgh office and can be full time or part-time.
In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.