Contract Clinical Study Manager - Top 10 Pharma - Fieldbased - UK

Job Reference: #67843 Add to saved jobs

  • Location United Kingdom
  • Contract
  • Sector Pharmaceuticals

Job Summary

Clinical Study Manager, Clinical Study Manager, Clinical Development, Clinical Manager, Local Study Manager, Pharmaceutical, Field-based.

Job Overview

A new opening has become available for a long-term, 12-month contract/freelance opportunity for an established clinical research professional (Global Clinical Lead) to join this Top 10 Pharmaceutical company.



You will be joining the Global CVRM function, responsible for managing multiple local studies, from the operational study start to, implementation and closure.



The position will suit an experienced Clinical Study Manager/Local Study Manager consultant with solid experience in managing early-phase clinical studies.



Please note: this role is fieldbased with regional travel.



COMPANY BACKGROUND:



Sitting within the world’s leading players in the pharmaceutical industry, this company continue to develop and offer a magnitude of innovative medicines onto market, ranging from Oncology to Cardiovascular, Respiratory, and more therapeutic areas. With a global reach employing over 50,000 people over 30 countries, they provide a network of expertise. They also have a strong base of contractors, with over 800+ at their UK sites, and so are viewed as an essential asset to their business model.



ROLE RESPONSIBILITIES:



Chance to join this top-10 Global Pharma on an initial contract basis, paying a competitive daily rate. The position will be based at their Cambridgeshire site (currently remote until further notice).



Leading multi-disciplinary and multi-national study delivery teams in the planning and delivery of CVRM studies.
Lead or support study related change management within business strategy.
Ensure compliance with SOPs as well as international and local regulations.
Lead and manage study stakeholders and CROs.

Skills Required

SKILLS DESIRED:



Strong clinical operations background 5+ years.
Local Study Management experience 3+ years.
Sound understanding of international guidelines within the drug development industry.

Contact Details

Location – Fieldbased

Length – 12-months with potential extension.

Rate: Circa 450 per day.



Looking for those who can ideally start within the next 4 weeks, looking to shortlist and interview in the coming week apply below now.



Associated keywords: Clinical, Clinical Trial, CVRM, Cardiovascular,, Regulations, Project Management, Project Lead, Drug Development, Study Manager, Late-phase, observational, Pharma, Pharmaceutical, Cambridge, Cambridgeshire.

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