CK Clinical top jobs: August 2017

This month, we have a range of exciting and unique roles from a Regulatory Submissions Specialist to the Senior Manager of Global Safety Compliance, take a look at these roles here:


Senior Manager of Global Safety Compliance

Location: Maidenhead
Salary: £90,000, car allowance, 10% bonus, stock, 2 days remote working
Reference: 39889

  • A new permanent opportunity within a team of four, reporting to the Director of Safety Compliance
  • This role is not a hands on CAPA management role and is more about giving guidance, following up, setting metrics and generally looking at continuous improvement
  • You can become more of an enabling function so there are plenty of opportunities to become a driver of change.
  • The right person should have a good PV background at a senior / above country level, or you might come from an auditing background
  • Understanding of PV systems and what a QMS (Quality Management System) is and why it’s important

Click to apply


Regulatory Submissions Specialist

Location: Uxbridge
Salary: Competitive
Reference: 39863

  • Working for an innovative global biopharmaceutical company with a focus in Oncology
  • Using electronic publishing systems, support the regulatory teams with the preparation and coordination of submissions
  • You will be responsible for global submissions including the US and EU regions
  • If you have significant regulatory operations experience across multiple regions then this would be an opportunity to join a fantastic team

Click to apply


Global Director Medical Communications, Oncology

Salary: €140 circa
Location: Frankfurt area Germany / Boston area US
Reference: 39497

  • A rare opportunity to join lead a Global communications team of nine
  • This is a high visibility and high impact role working with a wonderful product portfolio
  • A strategic and tactical role with the chance to develop and lead a highly capable and ambitious group
  • You will have extensive experience within medical publications and communications as well as both global and management experience

Click to apply


Head of EMEA Medical Affairs Oncology

Location: Hertfordshire
Salary: Competitive
Reference: 39579

  • A chance to lead an International Medical Affairs group within Oncology, working on an existing and growing portfolio of medicines
  • You will have first and second line reports (30+) and lead the strategic and operational activities of the department
  • You will be a GMC Registered Physician with significant experience of oncology and medical affairs, ideally with management experience

Click to apply


EMEA Medical Manager, Neurology 

Location: Hertfordshire
Salary: Competitive
Reference: 39741

  • An opportunity to join an EU+ medical affairs group, assisting the Head of with strategy creation and implementation
  • Working across the neurology portfolio you will work within dementia, sleep and epilepsy amongst other therapy areas
  • You will be a Physician with experience of Neurology (ideally a neurologist) and working within medical affairs / clinical development

Click to apply


Clinical Trial Assistant

Location: Crawley
Salary: £25000-30000
Reference: 39834

  • Exciting opportunity for a Clinical Trial Assistant to join a well established and growing Clinical Research Association.
  • Role is office based in CrawleyInvolves working specifically within Oncology
  • Involves providing administrative support to project teams in conducting and collating information from feasibility studies.
  • The CTA will work closely with Clinical Project Managers, Clinical Research Associates and other members of the Clinical Operations team.
  • Provide administrative support to project teams in conducting and collating information from feasibility studies.

Click to apply


Clinical Research Scientist

Location: Hertfordshire
Salary: Competitive
Reference number: 39569

  • An interim position with a global, mid-sized pharmaceutical company
  • You will provide scientific support for late phase oncology clinical trials
  • Duties will include review of Clinical Trial Protocols, analysis of study data and input into the preparation of Clinical Study Reports
  • Candidates will require late phase oncology experience

Click to apply


If these roles are not quite right for you, take a look at our other roles here.

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