Clinical Research Associate

Employer
Seuss +
Location
Netherlands
Salary
Competitive
Start date
14 Jan 2022
Closing date
13 Feb 2022

View more

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

This is an exciting opportunity to work for a full-service, international, niche CRO specialising in medical devices on a permanent contract.

Is this is career challenge you've been looking for?

Work for an organisation that recognises your expertise

As newly appointed Clinical Research Associate, you'll be responsible for establishing, maintaining and supporting clinical trials in a diverse and dynamic environment.

Performing clinical trial oversight and study management while ensuring trial data is accurate, complete, and verifiable. Working to ensure that the trial conduct complies with ICH-GCP and other regulatory standards.

Do you enjoy?
  • Meticulous project planning and preparation?
  • Sourcing and compiling information?
  • Prioritizing tasks and initiating start-up tasks?
  • Working closely with Project Managers?
  • Participating in internal TMF reviews?
  • Assisting in administrative tasks for submissions?
  • Participating in project and investigator meetings.

The main duties of your new role:

  • Clinical trial oversight at investigational sites.
  • Reporting in accordance with SOPs and GCP for pre-study, site initiation, routine monitoring and close-out visits.
  • Collaboration with guide study investigators, coordinators, analytical services.
  • Data and protocol collection, review and verification.
  • Audit and inspection preparation.
  • Prepare submissions for the institutional review board, ethic committees and competent Authorization, and Drug Administration.
  • Preparation of confidentiality and clinical trial/investigator agreements.
  • Annual trial process reports
Your education and background:
  • B.A/B.S or equivalent experience in a (para)medical, scientific or health-related discipline or related work experience.
  • Min 1 year experience in clinical research or as a CTA or CRA.
  • GCP, IVH, E6 FDA proven knowledge.
  • Regulatory guidelines knowledge for medical devices.
  • Fluent English, both written and spoken.

Enjoy working in a diverse and dynamic organisation

Our client values teamwork and collaboration; you'll join an organisation that offers excellent compensations, pension schemes, life insurance and holiday allowance.

Our Recruitment Process

At Seuss+, We go beyond traditional recruitment; we work closely with you to ensure an unrivalled, personal candidate experience throughout our entire process.

Our strong client relationships allow us to fully support you through the recruitment process, providing you with all the role insight and knowledge you need.

Our recruitment process is entirely confidential. Your details will never be shared without your prior consent.

Company

Seuss+ is a life science consultancy that brings together expertise in HR and recruitment, outsourcing and procurement, marketing and sales, training, and technology.

We help professionals find life-changing career growth in exceptional life science and pharma jobs.

We go beyond traditional recruitment; we work closely with you to ensure an unrivalled, personal candidate interview experience throughout our entire process.

Our recruitment process is entirely confidential. Your details will never be shared without your prior consent.

Discover more about Seuss+ and our unique founding story https://www.seuss.plus/about/

Find Us
Website:
Telephone
+ 31 (0) 20-2900016
Location
Zekeringstraat 7A 1014 BM
Amsterdam
NL
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