ICON Clinical Research

IHCRA

Location
Milan
Salary
Competitive
Posted
18 Jan 2021
Closes
12 Feb 2021
Ref
1JR069275
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Job Advert Posting

In House Clinical Research Associate (IHCRA)

Office based in Milan

This is an opportunity to work for ICON Clinical Research. With a track record for successful analysis and extensive scientific publication, the ICON Clinical Research division delivers high-impact evidence that explores and demonstrates the value of pharmaceutical, biotechnology, consumer healthcare and medical device products in all global markets, with a focus on maximising return on investment.

Our global team of experts provide a full spectrum of market-leading clinical studies to support our clients' product lifecycle. We now seek to recruit a dedicated, hardworking Clinical Research Associate, at a Entry Level to join our busy team in our Warsaw office.

Overview of the role

You will be responsible for in-house contact and site management for the assigned sites and assist with the follow up and resolution of actions in consultation with CRA. Site management will include communication with the site on recruitment status, follow-up on data entry and queries, obtaining site updates to provide to the project teams and the tracking of discussions.

You will work with the Monitoring CRA to address the Clinical Data Analyst findings.

You will be responsible for the quality and completeness of data in CTMS and the Trial Master File.

To apply you should have a Life Sciences degree, having previous experience in Clinical Research is an advantage but not essential. Excellent communication and relationship skills. You will be meticulous and organized and be able to follow an issue to resolution. You will need to take ownership and accountability for your sites and deliver to a high standard.

You will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner. You should be able to produce accurate work to tight deadlines within a pressurised environment.

You will have the opportunity to progress your career and may wish to move into CRA monitoring, SSUA Project Management or into other related areas where you can further develop your skill set.