Project Managers and CRA's

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We are currently recruiting for two positions and are interested in speaking with applicants who have a minimum HBO (para-)medical education and who are looking for an exciting job in a small, dynamic, fast growing international company.

Experienced Clinical Research Associate (CRA) for 0,8 – 1 FTE

and

Experienced Project Manager (PM) for 0,8 – 1 FTE

 

More details about Clinical Research Associate:

We are looking for a candidate with a minimum of 2 years experience as a CRA. Without experience it is not necessary to apply for this job.

 

Job purpose: This role will identify, select, initiate and close-out investigational sites for clinical studies ensuring adherence to applicable regulations and principles of ICH-GCP.

Responsibilities & Accountabilities:

  • Assist team members to facilitate the successful completion of the clinical program
  • Understand and adhere to ICH/GCP regulations and Venn Quality Documents and processes
  • Prepare/assist in Ethics Committee/Institutional Review Board (IRB) and regulatory authority submissions and follow the process until approval
  • Prepare and coordinate feasibility analysis
  • Mentor and train junior staff
  • Support the project manager as required
  • Monitoring of clinical trials

 

More details about Project Manager:

We are looking for a candidate with a minimum of 5 years experience as a Project Manager in Clinical Research and in leading projects.

 

Job purpose: This role will coordinate and manage the activities of the studies, costs and project team to agreed timelines adhering to SOP’s and ICH-GCP, to include, effective management of assigned staff to ensure continuous development, high performance and low turnover is maintained.

Responsibilities & Accountabilities:

  • Manage/coordinate project team(s)
  • Proactively manage the sponsor(s) and its expectations
  • Assist the senior management in process improvement efforts
  • Take responsibility as mentor and trainer for CRAs/CTAs of any level
  • Acts as the primary project related representative of the company

 

Key traits for Venn Life Sciences are:

  • Personal commitment to high-quality data
  • Positive, “can do” attitude
  • Excellent organizational skills
  • Ability to embrace change
  • Desire to stay engaged
  • Know-how to prevent personal burnout
  • Flexible travel strategies

 

We are offering a flexible job with good opportunities and a lot of training and chance to develop yourself. You must have a drivers license and be able to visit sites in The Netherlands, Belgium and other countries. Also you will want to work hard in a stimulating environment.

Fluent English in speaking and writing is a must and if you also speak French this is a bonus.

 

For more information about our company you can refer to our website: www.vennlifesciences.com

 

For questions about the content of the jobs, you can contact our office at

0031-(0)524-712 456 and ask for Graciëlle Schutjens, Head Clinical Operations (or in her absence Barbara Oosting, HR & Finance manager).

 

We would like to receive your English CV and motivation within 7 days after publish date.

 

Acquisition for this advertisement is not appreciated.

 

 

 

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