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Freelance Clinical Development Manager / Global Study Leader (GSL) – Global Pharma – 12-24 months, full-time – Office-based in Warsaw, Poland

Company: SRG Clinical
Location: Warsaw, Poland
Reference: temp-GSL-Warsaw2018-Arnaud@SRG
Closing Date: 10 Aug 18
Type: Temporary
Salary (£): Competitive
Benefits: Long-term contract 12 to 24 months, Generous rate, One of the fastest growing Clinical Group worldwide

Job Summary:

A Global Pharma has entrusted me to find Clinical Development Managers / Global Study Leaders (GSL) to add to their fast growing and exciting clinical group in Warsaw, Poland. While several GSLs will be hired on a permanent basis, I am specifically looking for freelancers here, for 12-24 months on a full-time basis

Requirements:

Freelance Clinical Development Manager / Global Study Leader (GSL) – Global Pharma – 12-24 months, full-time – Office-based in Warsaw, Poland

Freelance role

Long-term contract 12 to 24 months

Generous hourly rate

No Local (Polish) language requirement

One of the fastest growing Clinical Cluster worldwide

Working together on an ambitious project, I am suporting a key strategic partner in their search for numerous freelance Clinical Development Managers / Global Study Leaders (GSL). The successful candidates will work alongside their highly productive and booming team in Poland.

This is a rare opportunity to work on global projects and get exposure to sensational product pipelines! As mentioned above, the company operations are growing very fast in the region so applicants from outside Warsaw or Poland are welcome to apply, even without polish speaking skills.

The GSL will lead the Delivery of Scientific Global Portfolios and oversee Vendor and CRO.

Responsibilities (not limited to):

  • Lead and manage a clinical delivery team to operationally deliver clinical studies or clinical project activities
  • Lead the operational delivery of clinical studies, engaigin with a team of experts from the study specification to the final clinical study report and archived master file
  • Provide input into study feasibility and study specifications, and produce essential documents including the authoring of clinical study protocols across both interventional and non-interventional studies
  • Management of changes to project scope and costs (including CRO and other vendors change orders) and reporting project status

Requirements:

  • University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research
  • At least 5 years’ experience from within the pharmaceutical industry or similar organization
  • Extensive knowledge of clinical operations, project management tools and processes
  • Good experience of clinical development / drug development process in various phases of development and therapy areas
  • Project management certification is desirable

About SRG:

SRG is the market leading supplier of Clinical and Drug development recruitment services to the Life Sciences industries. By putting people at the heart of what we do we are the catalyst that connects the best talent with organisations in the pursuit of ‘Creating Tomorrow’s World’& helping patients world-wide.

HOW TO APPLY?

For an immediate consideration please press 'apply' now, alternatively contact Arnaud Heroult on +44 (0)203 096 4712 and get more information about the role. 

Our team at SRG Clinical also cover roles in Biometrics, Medical Affairs, Clinical Operations, Medical Information, Pharmacovigilance and Regulatory affairs so do not hesitate to call me at +44 (0)203 096 4712.

Fancy getting rewarded?

We find that good people know good people. So when you recommend a friend to SRG and we place them in a contract or permanent job, you could earn a bonus of up to £1,000 of Red Letter Days vouchers as a thank you.

https://www.srg.co.uk/en/job-seekers/referral


The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency

 

Key words: CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Permanent, Freelance, Contract, Full-time, Temporary, Project Management, Senior, Manager, Site Manager, CPM, Clinical Project Manager, Study Manager, Project Delivery, Clinical Trial Manager, CTM, Study Director, Project Leader, Clinical Development, Global Study Leader, Clinical Site Manager, Clinical Operations, Clinical Team lead, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology, hematology, orphan diseases, nephrology, musculoskeletal, endocrinology, gastroenterology, infectuous diseases, Budget, Protocol, Vendor oversight, Vendor managment, Vendor meeting, Line Management, Ethics submissions, Regulatory body

Apply for this job: Freelance Clinical Development Manager / Global Study Leader (GSL) – Global Pharma – 12-24 months, full-time – Office-based in Warsaw, Poland

Contact Information:

Address:  Head Office
SRG Clinical 9 Devonshire Square London United Kingdom
EC2M 4HP
England
Tel:  +44 (0)203 096 4700
Website:  Visit Our Web Site

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