Clinical Research Associate - Strategic Solutions

We are looking for a homebased Clinical Research Associate (CRA), to work with a single sponsor fully outsourced to their team.
The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle. Key responsibilities include:


Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.



You will receive the support you need to develop personally and professionally and work in an environment where you matter. This sponsor is unique in that you will be treated as a full member of their global Clinical Trials Team. As a CRA, you play a key role in our sponsor’s drug development process and are expected to push forward together - united in solving problems, developing close site relationships and reaching the end goal.
Qualifications
To enable success in this position you will have:
At least 1 year of experience working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
Experience working on Oncology trials or complex studies would be an advantage for this role.
A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential
Fluency in Swedish and English is essential
You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
We have a number of roles open. Homebased in Stockholm, Mälardalen (Uppsala preferred) and Southern Sweden (Gothenburg/Lund/Malmö)