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Clinical Trial Assistant III - Paris - Biotech

Employer
Barrington James
Location
Paris (Département), Ile-de-France (FR)
Salary
Competitive
Start date
24 Mar 2023
Closing date
23 Apr 2023

View more

Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

The company I am working with is a small leading Biotech with a focus on developing drugs to treat neurovascular diseases, this rapidly expanding biotech company has a pipeline of seven robust drug candidates. As a member of the team, you'll have the opportunity to work closely with the VP, CEO, and other senior leaders, while reporting directly to the Head of Clinical Operations - positioning you for growth and advancement within the company.

We are currently seeking a Clinical Trial Assistant with at least 3 to 5 years of experience in the biotech industry to manage the daily operations of clinical trials. The ideal candidate should have experience with eTMF, including quality assurance and access control, as well as thorough familiarity with ICH and GCP requirements.

Responsibilities:

  • Manage clinical papers' daily operations to ensure quality control and compliance with ongoing clinical trials
  • Ensure accuracy of documentation and efficient sharing of information across sites, CRAs, project managers, and trainers
  • Communicate with investigators and get around administrative obstacles
  • Work on vendor contracts, invoices, and other supporting document tools
  • Create and maintain eTMF (Veeva)
  • Create, deploy, and maintain supporting tools and documentation
  • Administer contracts and monitor investigator payments
  • Ensure document quality control
  • Make and keep up with graphs and timetables
  • Connect with sites and CROs for document deployment and retrieval

Requirements:

  • Autonomy and proactivity in dealing with administrative documentation for a dedicated Clinical Trial
  • Excellent communication abilities
  • Encompass standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements
  • Ability to provide efficient updates on trial administrative progress and visibility to project management
  • Experience in Cardiovascular and Neurovascular Trials, with Emergency Trial and Stroke Experience a bonus
  • Fluency in a third language and spoken and written English are excellent to haves
  • Great soft skills including team spirit attitude, flexibility, methodology, tenacity, and openness to feedback
  • Motivated by stressful challenges in clinical trials management and ready to be a pivotal team member

This position reports to the Head of Clinical Operations and does not involve management responsibilities. The seniority level and corresponding job title will depend on experience.

If you are a highly motivated individual with a proven track record in clinical trial management and a desire to work in a dynamic, fast-paced environment, we encourage you to apply for this exciting opportunity.

Company

We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Company info
Website
Telephone
01293 776644
Location
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
GB

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