Clinical Study Assistant (TEMP)
Are you passionate about supporting groundbreaking clinical research?
The Clinical Study Supplies Assistant is a critical temporary role, providing essential operational, administrative, and coordination support to Clinical Study Supplies Managers. This dynamic position ensures the meticulous documentation, timely execution of all supply-related activities, and seamless communication with internal teams and external partners.
Are you available for the next 12 months,? Then join and be instrumental in advancing clinical research through flawless study supply management!
Company profile
Are you passionate about supporting groundbreaking clinical research?
The Clinical Study Supplies Assistant is a critical temporary role, providing essential operational, administrative, and coordination support to Clinical Study Supplies Managers. This dynamic position ensures the meticulous documentation, timely execution of all supply-related activities, and seamless communication with internal teams and external partners.
Are you available for the next 12 months,? Then join and be instrumental in advancing clinical research through flawless study supply management!
Job profile
The Clinical Study Assistant is responsible for operational and administrative support throughout the clinical study within the global clinical research team. The Clinical Study Assistant is a member of the wider team, including Study Managers, Study Researchers, Data Managers, and the Supplies team.Key tasks
- Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the applicable GCP guidelines and standard operating procedures;
- Prepare ISF (investigator site file) and TMF (trial master file) for the initiation of participating centers in clinical studies;
- Support the team with the financial management of the clinical studies;
- Support the team in contract management and vendor creation;
- Support the preparation and organization of internal and/or external meetings;
- Participate in the optimization of processes within the department;
- Act as a central contact for the clinical team for project communication, correspondence, and documentation;
- Support the team with any ad-hoc requests that come in internally and externally during execution of the study.
Requirements
- Completed medical, pharmaceutical, life sciences, logistics, or administrative education at MBO level or higher (Bachelor's or Master).
- BSc / MSc: 1–2 years of relevant experience preferred but not mandatory.
- MBO: Minimum 5 years of relevant experience preferred;
- Knowledge of GCP is preferred
Offer
Through our agency, you will receive a 12-month temporary contract.
There is a possibility that your contract will be renewed after these 12 months or that our client will make you an offer of a contract; however, we are not able to guarantee this.
- Salary will be between €3500 and €4000 gross a month, based on a full-time position (40 hours a week), and is based on education and experience.
- 30 Annual leave days;
- Travel expenses will be covered.
- Pension plan.
What will happen when you apply? Within four working days, we will let you know whether you are qualified for the position. If you do we will schedule an interview (digital or live). In this interview, we will inform you about the vacancy, the company, and the procedure. If we both agree this is a fitting opportunity we will introduce you to our client and continue to guide you through the whole application process. The Independent Recruiters Group has a large team of specialized recruitment consultants. Every recruiter has a strong focus regarding his/her field of expertise. This makes them the ideal sparring partner for both you, as the candidate, and the client.
