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.
Contact Information
- Send us an E-mail
info( at )vlsworldwide.com - Call us on
+353 12352620 - or click here to find your local office.
News and Highlights
- Venn Life Sciences is exhibiting at the DIA 5th Annual Read more...
- 2nd Annual Clinical Trials for Medical Devices. Taking place 22nd Read more...
Apply for a Vacancy
- Send your CV to:
careers( at )vlsworldwide.com
Have a Resourcing Need?
- Contact:
sabine.hutchison( at )vlsworldwide.com