Clinical Trial Assistant - Pharma - 12 month contract

Do you want to work on a broad Clinical Trial Assistant role with good chances of getting a permanent contract?

Our client is Pharma Company, specialized in Oncology, today working on a drug candidate for an Orphan disease. They are looking for a Clinical Trial Assistant that can assist their team that have oversight of the CROs that conduct their clinical studies.

Job Description

As a Clinical Trial Assistant it for our client you will collaborate with clinical oversight activities of clinical trials and can be responsible for the following:

• Reviewing Trial Master Files (TMFs)
• Editing clinical study related documents, e.g. Clinical Study Report Appendices.
• Supporting Head of Clinical Operations with Clinical related tasks like Standard Operation Procedure (SOP), process development and maintenance.
• Supporting team members by performing administrative tasks, e.g. managing meeting logistics and travel arrangements.
• Responsible for various trackers, e.g. Informed Consent Form (ICF)

Requirements

As a Clinical Trial Assistant for our client you would have to meet the following qualifications and skills:

• At least 2 years in clinical operations
• GCP experience
• eTMF experience (trial master files)
• Good experience of Microsoft office package
• Good spoken and written English

It is considered meritorious if you meet the following qualifications:

• Experience and knowledge in Oncology
• Fluent Swedish
• Sharepoint experience

My contact information

d.kolski@nonstopconsulting.com

Apply now sense interviews are happening immediately!