Reference Number: JO-1912-441758
Document Management Associate
Rate: Negotiable
Job Type: Permanent
Location: Cambridgeshire

Document Management Associate
Innovative Bio-pharmaceutical company
Attractive salary and benefit package

Regulatory Professionals are collaborating with clinical stage biopharmaceutical organisation who specialise in anti-body-based therapies are looking for a Document Management Associate to join their expanding team based in Cambridge. Within this role you will be responsible for the management and development of Regulatory Affairs paper-based and electronic document storage systems.
This is a unique opportunity and would be the ideal opportunity for an individual who has had prior document management or document control experience.

Job Responsibilities include:

Review existing documents management practises and/or procedures
Facilitate the identification of any requirement gaps
Prepare a list of licenses and subscriptions and establish prompts to ensure ongoing triggers for assessment/ maintenance
Prepare draft application forms
Develop and maintain tracking databases
Assist with preparation and support for Agency interactions

Candidate Requirements include:

Must be eligible to live and work in the United Kingdom
Structured, intuitive organisation of information
Experienced in working in a diverse environment
Clear demonstrable experience working in a team
Time management skills
Excellent written and verbal communication skills
Prior experience working on computer systems and document management software ie; Word, Excel & Powerpoint

If this position is of interest to yourself please call Sophie at Regulatory Professionals on 0118 952 2797 or forward your up to date CV to sophie@regulatoryprofessionals.com. Please note you must be eligible to live and work in the UK to progress.