Vacant job

Do you have a science degree and want to work practically with clinical studies? Do you thrive in a role with many contacts and clear processes? Then this could be your next step.

About the role

This is a full-time consultancy assignment starting immediately for a period of six months. You will be employed by Bravura and work as a consultant at Ipsen. There are good opportunities for extending the assignment.

About the company

Ipsen is an international pharmaceutical company headquartered in Paris. The company develops and commercializes medicines in several therapeutic areas and has products on the market globally.

In Sweden, there is a small but experienced Research & Development team based in Gothenburg. You will become part of Clinical Development Operations – a department responsible for planning, conducting, and closing clinical studies according to schedule, budget, and regulatory requirements.

Responsibilities

As a Clinical Trial Associate, you provide support to Clinical Trial Managers and global study teams. The role is operational and administrative with a strong focus on structure, quality, and collaboration. You are involved in several parts of the clinical trial process and contribute to ensuring that studies are conducted correctly and efficiently.

You work continuously with reviewing clinical documentation, reports, and data, ensuring that information is accurate and up-to-date in relevant systems. The role also involves working with eTMF, invoice management, and support during meetings. You have many contacts, both locally and internationally, and work closely with your colleagues in the team.

Examples of tasks:

• Support Clinical Trial Managers and global study teams
• Review and quality-assure clinical documents and data
• Work with eTMF and ensure correct documentation
• Manage and approve invoices related to studies
• Participate in and support internal and external meetings

Education, experience, and personal qualities

• University education in biology, biotechnology, chemistry, pharmacy, or another relevant natural science field
• Experience from the pharmaceutical industry is advantageous
• Good knowledge of Swedish and English, both spoken and written
• Good computer and system skills

To thrive in this role, you are structured and meticulous, with the ability to take responsibility for your tasks and drive them to completion. You work methodically and are good at creating order even when multiple things are happening simultaneously. At the same time, you are communicative and comfortable collaborating with others, both locally and internationally. You appreciate working in a team, are helpful in your approach, and contribute to good collaboration in the office.

Other information

Start: Immediately
Location: Gothenburg
Salary: According to agreement

We use a competency-based methodology in all recruitment processes to ensure unbiased selection. We also work with continuous selection, which means we remove the ad when enough candidates have applied. If you are considered for the role, we will contact you for a first phone interview. Regardless of whether you proceed in the process or not, you will receive feedback on your application.

Do you have questions? Feel free to reach out!

📧 [email protected]

📞 010-171 47 10

We recommend applying immediately as we conduct continuous selection.

We look forward to receiving your application!

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