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Vacancy summary

Reference: 07703

Job Type: Permanent

Date Posted: 5 April 2019

  • People centric organisation with a focus on excellence
  • Good location coupled with a modern working environment
  • Global biotechnology company

Senior Medical Writing Scientist 

A global biotechnology company who are a market leader in their therapeutic area need a Senior Medical Writing Scientist who will take ownership of creating clinical regulatory documents and regulatory submissions. You will be passionate about science and operating within an environment of excellence. Our client has a patient focused approach and is dedicated to developing innovative drugs to combat this rare disease and you will play an important part in delivery of their company goals and strategy.

KEY RESPONSIBILITIES:

  • Creating clinical study protocols and reports, investigator’s brochures and regulatory submissions and ensuring consistency and compliance within the documents
  • Act as a subject matter expert fielding queries from within the team and other internal stakeholders
  • Analysing and interpreting data
  • Supporting study projects, plans and statistical output
  • Taking part in product development plans
  • Assisting in in creating SOPs and related procedures

CANDIDATE:

  • You will hold a PhD and strong relevant experience working within Biotech and Orphan Drugs
  • Strong experience in writing and editing clinical regulatory documents
  • Ability to analyse data and solve the conflicts
  • Project management skills
  • Working collaboratively
  • Strong communication skills

The company pushes continual professional development, offers an excellent benefits package and a modern working environment.  

Park Street People Ltd does not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and complies with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.

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