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
NonStop Recruitment
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 project lead - 100% home office

Clinical Operations Manager - start up
Belgium
Biologielaborant
Germany
Study Start-Up CRA - Global CRO
Germany
CTC - develop your career in a growing company
Belgium
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.

Senior SSU Specialist - Global CRO



Business Type: Clinical Research Organisation
Job Type: Clinical Study- Trials
Job Level: Experienced (non manager)
Position: Full Time
Location: Belgium
Reference: JM 311921 6
Closing Date: 31/01/22
Job Details:

Senior Study Start-Up Specialist

Have you been working in Study Start Up and looking for the next move in your career? Look no further.

My Client is currently looking for a Senior Study Start-Up Specialist to join their team in Belgium fully remotely! They are a Global Biotechnology company that was founded over 30 years ago, now with offices in Europe, America, Australia and more. They are consistently being recognised as one of the top places to work and to prove that they have been on the Science Magazine''s ''Top Employers'' list for over 10 consecutive years. With more than 60 clinical trials running globally, this opportunity will allow you to have an intense but pleasant experience all while learning from the best in the industry!

Responsibilities:

- Perform all kinds of Study Start Up activities including feasibility, site identification etc.
- Perform timely and accurate data entry of all relevant study start-up activities into the appropriate CTMS
- To be familiar with ICH GCP, relevant country regulations/guidelines, and SOPs
- Perform regulatory document maintenance; amendments, periodic updates, and safety letters, where applicable

Requirements:

- 2-4 years of experience of working in site start up (Pharmaceutical or CRO)
- Experience in Oncology studies is a essential
- Working knowledge of ICH-GCP guidelines, local and international regulatory requirements is essential
- Fluent in English, Dutch and French

If you think you could be the person for the job please apply here or alternatively on the NonStop Consulting website or contact me directly on my LinkedIn, Jakub Morszczyzna, by phone on +44 207 234 0550 ext. 3602 or E-Mail j.morszczyzna@nonstop-recruitment.com. If, however you feel like the job is not for you or you are not available, please feel free to share it with your friends / colleagues who could be interested and help out your network!

NonStop Consulting is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.



Posted: 24/01/2022 | NPJ Ref: 296169
line graphic

Compatible with:

JobMate   Broadbean   Idibu

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