Freelance Clinical Trial Associate - UK - CRO (Vaccines)

Freelance Clinical Trial Associate - UK - CRO (Vaccines)

i-Pharm Consulting are seeking on behalf of a leading mid-sized CRO a Freelance Clinical Trial Associate to support the clinical operation teams management of a large scale vaccines trial in the UK.

THE COMPANY:

Leading mid-sized CRO specialising in a broad range of therapy areas. i-Pharm has been a dedicated recruiter for this client for a number of years and have had great feedback on the company's career progression, culture and job satisfaction from candidates placed.

THE ROLE:

• Support the clinical operations team consisting of CRAs and Project Managers
• Prepare and maintain the eTMF
• Coordinate Ethics Committee submissions with support of the Lead CRA
• Assist with CRAs and Project Managers with study budget negotiations
• Complete internal administrative tasks
• Good knowledge of ICH-GCP Guidelines
• Update Clinical Trial Management systems (CTMS)
• Co-ordination of Clinical Trial supplies
• Study documentation filing
• Coordination of meetings and minutes taking

LOCATION:

• UK - Home Based

RATE:

• Competitive daily rate

DURATION:

• Start January 2021
• 12 month contract
• 37.5 hours per week (1FTE)

EDUCATION REQUIREMENTS AND QUALIFICATIONS:

• Life Science Degree or Nursing background
• 2 + years experience in a CRO or Pharma/Biotech company minimum
• Ability to work independently and effectively within a fast paced team
• Good knowledge of the Electronic Trial Master File (eTMF)
• Must have experience using Veeva Vault
• Ability to manage multiple and varied tasks
• Strong computer skills including the knowledge of a Clinical Trial Management System (CTMS)
• Experience in vaccines, virology, infectious diseases or respiratory trials is sought after but not essential
• Excellent verbal and oral English
• Goodorganizational skills and attention to detail

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 Lauren McQuade on +44 (0)20 3189 0488, or email lmcquade@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEYWORDS:

Clinical Trial Administrator / CTA / Clinical Trial Assistant / Clinical Trial Associate / Clinical Trials / Clinical Research / Contract Research Organisation / CRO / Clinical / Pharmaceutical industry / Contract / Contracting / Freelancing / Freelance / Home Based / COVID / Vaccines / CPA / Field Based / UK