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Regulatory Writing Project Manager - Alderley Park, Cheshire - Bioscript Regulatory



Business Type: Medical Communications Agency
Job Type: Medical Writing and Editorial, Project Management, Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Location: North West
Reference: reg-wri-proj-man
Background:

Due to the continued expansion of the Bioscript Regulatory group we now need a dedicated project manager to assist in the coordination and delivery of our products to our customers. Do you have a proven track record in project management in regulatory writing or a related field? Would you like to gain more experience in a new environment? If so, we can offer you opportunities in a forward-thinking, friendly and dynamic agency.

Location: Alderley Park, Cheshire

Job type: Permanent. Full-time or part time (30 hours per week).

We encourage our employees to maintain a good work-life balance and are open to discussions around flexible arrangements. Benefits: Competitive salary, profit-related bonus, pension, health insurance, 25 days’ holiday, and much more! Company information Bioscript Regulatory is part of Bioscript Group, a full-service, global healthcare communications agency delivering communication planning, publications, medical meetings, digital programmes, health economic and regulatory services to pharmaceutical companies. We have grown steadily over the past 12 years, adding new clients and talented new staff every year.

Duties and responsibilities of the role

As a Regulatory Writing Project Manager, you will:
  • Coordinate and support the smooth running of regulatory accounts so that the objectives of the clients and Bioscript are met.
  • Monitor Writing and Quality Control resources in support of the Regulatory team
  • Assist in preparation of pitches for new work, including development of timelines and budget estimates
  • Prepare budgets and monitor financial status of each regulatory project ensuring margins are maintained and that early action is taken with clients where project specifications change.
  • Support the finance team with forecasting and assisting with the smooth running of the financial process.
  • Manage logistics to support the Regulatory team’s activities including training, internal meetings and client meetings.
Requirements
  • Experience of project management in the pharmaceutical or healthcare industry.
  • Excellent interpersonal and communication skills (verbal and written).
  • Proven ability to provide project and account management for large projects, liaising effectively with project teams, successfully delivering projects on time and on budget.
  • Experience of budget development and financial management.
  • The confidence to take responsibility for the organisation of complex deliverables, and the ability to prioritise between multiple projects.
Interested?

Send your CV and a brief covering letter to careers@bioscriptgroup.com

All offers of employment are subject to candidates’ ability to provide suitable documentary evidence oftheir right to work in the UK. 

Posted: 22/01/2018 | NPJ Ref: 204825 | NPJ Original URL
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