Freelance Study Start Up Lead - EU & US - CRO - Home Based

3 days left

Location
Spain
Salary
Negotiable
Posted
11 Jan 2021
Closes
25 Jan 2021
Ref
YM02899
Contact
Youssef Maachou
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)

Freelance Study Start Up Lead - EU & US - CRO - Home Based - Anywhere in Europe


i-Pharm Consulting are seeking on behalf of a mi-size full service CRO a Freelance Study Start Up Lead.

THE ROLE:
Initial 6 month contract. Fully home based anywhere in Europe. This role will see you leading the oversight of study start up activities for assigned studies across Europe.

Other duties include:

  • Accountable for end-end study start up activities for assigned Global clinical trials
  • Oversee the study start up activities of SSU specialists to ensure timelines and deliverables are met
  • Managing the coordination and oversight of site identification, site contracts negotiations and central and local EC/CA submissions
  • Serve as the primary point of contact for all start up activities for assigned projects
  • Develop SOPs and best practice guidelines relating to assigned studies
  • Contribute to the proposals and bid defence meetings
  • Develop global SSU and Site Activation plans for assigned studies

LOCATION:
Home Based - anywhere in Europe

RATE:
Competitive hourly rate


REQUIRED:

  • Life sciences degree
  • 5 years within Pharmaceutical/CRO industry
  • 2+ years within EU/global study start up and site activation experience is essential
  • Good knowledge of clinical research processes including ICH GCP
  • Excellent written and verbal English
  • Ability to communicate clearly with internal and external stakeholders
  • Ability and willingness to mentor junior members of staff

About i-Pharm Consulting
i-Pharm Consulting is a global specialist recruitment company servicing the pharmaceutical industry. 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 Youssef Maachou on +31 20 808 14 84, or email ymaachou@i-pharmconsulting.com. If this role is not suitable, Youssef is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

Keywords

Pharma / pharmaceutical / biotech / manufacturing / clinical / distribution / medical devices

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