Freelance Study Start Up Lead - EU & US - CRO - Home Based
- Company
- i-Pharm Consulting
- Location
- Spain
- Salary
- Negotiable
- Posted
- 11 Jan 2021
- Closes
- 25 Jan 2021
- Ref
- YM02899
- Contact
- Youssef Maachou
- Discipline
- Clinical Research, Study Start Up
- 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.
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