This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
i-Pharm Consulting
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Clinical Study Manager- Remote Role
United Kingdom
Country Study Manager- Remote Role
United Kingdom
TMF Operations Manager - Biotech - Freelance
London
Freelance Senior Clinical Trial Manager - Cell Therapy Oncology
London
Vigilance Specialist - German Switzerland - High Tech products
Switzerland
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
This job has expired. Click here to view similar jobs.

Clinical Project Associate - Pharma - London (Part Time)



Business Type: Pharmaceutical Company, Biotechnology Company, Drug Development Company, Freelancer, Pharmaceutical Services
Job Type: Clinical Research, Clinical Operations, Clinical Study- Trials, Clinical Administrator - CTA, Feasibility Management
Job Level: Experienced (non manager)
Position: Part Time
Salary: Up to GBP220 per day
Location: London
Reference: 030720LMCQ1
Closing Date: 10/07/20
Job Details:

Clinical Project Associate (Part Time) - Small Pharma - Central London

i-Pharm Consulting are partnering exclusively with a Small Pharmaceutical Company in Central London who are seeking a Clinical Project Associate to join their Clinical Operations team. This pharmaceutical company develops novel treatments within the area of Women''s Health.

THE ROLE:

  • Reporting directly to the Director of Clinical/Medical
  • Provide support in the management of CROs and other Vendors
  • Assist the Project/Regulatory Lead in the creation of study related materials
  • Tracking of invoices and study payments
  • Management of TMF including generation of documents and TMF review
  • Assist in the preparation of meeting agendas, minutes taking and action item tracking
  • Support all aspects of study progress from planning to close out
  • Support all regulatory requirements (EC submissions)
  • Contract, budget, and invoice management
  • Co-monitoring alongside Regulatory Lead (international)

LOCATION:

  • Central London - Office Based
  • (Home based during COVID as per government regulations)

RATE:

  • Competitive daily rate

DURATION:

  • 6 month rolling contract
  • 3 days per week initially with the opportunity to increase to full time after initial assignment (negotiable)

EDUCATION REQUIREMENTS AND QUALIFICATIONS:

  • Bachelor''s degree or higher (Scientific or healthcare discipline preferred)
  • Work experience:
    • 2-3+ years'' experience in drug development in the pharmaceutical industry
    • OR
    • 1+ year in industry coupled with NHS or Academia experience
  • Experience working in a clinical operations / clinical project management
  • Ideally exposure to international/global clinical trials
  • Exposure to site activation/SSU activities
  • Knowledge of ICH GCP
  • Proficiency in Microsoft Word, Excel and PowerPoint
  • Must be a self-starter with the ability to multi-task and adapt to a start-up feel company environment

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 / CPA / Clinical Project Assistant / Clinical Project Associate / Junior Project Manager / Pharmaceutical / Biotech / Biotechnology / Women''s Health / Urology / CRO / Central London / Soho / Mayfair / Marylebone



Posted: 03/07/2020 | NPJ Ref: 255838
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing




Credit cards image