Study Start Up Associate I

Study Start Up Associate I

Location: Warsaw, Poland

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

·         Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements

·         Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager – Central Services or Designee.

Role Requirements

·         A high school diploma or local equivalent

·         Bachelor’s Degree preferably in Life Sciences

·         Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities.

·         Experience of Clinical Trial operations

·         Experience meeting regulatory and ICON guidelines

·         Proficient project management skills.

Benefits of Working in ICON

Other than working with an outstanding team of friendly and ambitious people, we also offer a very competitive benefit package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

What’s Next?

Following your application, you will be contacted by one of our dedicated recruiters and if successful, we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to delivering a workplace free of any discrimination or harassment.