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i-Pharm Consulting
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Job Details
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Study Start-Up Specialist - Amsterdam



Business Type: Clinical Research Organisation
Job Type: Clinical Study- Trials, Clinical Administrator - CTA, Contracts - Proposals
Job Level: Experienced (non manager)
Position: Full Time
Location: Netherlands
Reference: CNOB737
Closing Date: 21/08/19
Job Details:

i-Pharm consulting is seeking an experienced SSU specialist to join a global CRO and be based in Amsterdam. The ideal candidate will have experience performing local start up activities including ethics and regulatory submissions

LOCATION
Amsterdam - Home or Office Based

RESPONSIBILITIES
* Reviewing essential document packages for site activation

  • Preparation and submitting of Central EC Applications, Local EC Applications, - RA Applications, and other local regulatory authorities or hospital approval submissions as required
  • Reviewing Informed Consent Forms
  • Negotiating terms and budget of the contract with Investigator Sites

REQUIREMENTS
* SSU experience within clinical research
* Knowledge and understanding of GCP
* Excellent Communication skills
* Working knowledge of Microsoft Office
* Fluent Dutch
* Right to work in The Netherlands

BENEFITS
* Competitive Salary
* Healthcare
* Pension
* Flexi Benefits

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com


TO APPLY

If you would like to discuss this vacancy further, please call Team Leader Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.com. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS
Good Clinical Practice / GCP / International Conference on Harmonisation guidelines / CRO / Contract Research Organisation / Office Based / Study Start-Up / Admin / Assistant / Leeds / SSU / Site Contracts / Contract negotiation / Budgets/ Netherlands / Amsterdam / Ethics Submissions / Regulatory Submissions / Biobank Submissions /



Posted: 14/08/2019 | NPJ Ref: 240290
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