Job Description
Job Overview
We have an exciting opportunity for an Assistant Study Coordinator to join our friendly Toxicology Administration & Reporting department. This role is full time, on site (with hybrid options after a period of training), and is located in our world class facility in Tranent (EH33 2NE).
The role is well suited to an individual who enjoys collaborating with others, organisation, working to tight timescales, and who would like to build a career supporting scientific studies. You will work closely with Study Directors and cross functional teams, and have the chance to grow and progress through a clear departmental development career pathway.
This role is offered Full time, the Salary of £25,352.56 per annum as well as 29 days paid Holidays, Pension, Private Healthcare, Health Insurance, Employee discount scheme, Free Gym on site, Cafeteria with great food, Free onsite parking and more.
Key Responsibilities and Experience
Key Responsibilities
- Work collaboratively with Study Directors to develop study protocol and other relevant study documentation
- Set up, schedule and assist in the running of a variety of Toxicology studies.
- Liaise with various contributing areas to the study to schedule in all key activities required.
- Serves as a contact, along with the Study Director, in communication and interactions with other departments, with assistance as applicable
Experience and requirements
- Experience in a busy office environment.
- Strong technical experience in Microsoft Office.
- Proven organisational skills with the ability to work within tight timeframes.
- Good, confident communication and people skills which enable you to effectively collaborate with internal/external employees of all levels.
- A proactive working style with the ability to plan ahead.