Site Management Associate I

Site Management Associate I

Office based in Barcelona

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas including Oncology, Vaccines, CNS, Cardiovascular, and Pain. We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally. We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients.

The Site Management Associate is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations. The responsibilities of this position include, but are not limited to:

• Identifying, training/initiating and closing out study sites.
• Conducting remote site monitoring visits and/or targeted on-site visits as needed.
• Conducting remote site management activities.
• Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.

A Bachelor's degree in the life sciences, expertise with regulatory guidelines and clinical terminology, and demonstrable strong site management experience will ensure your success on our team. This would be a great opportunity for someone with the skills and background of an in-house CRA looking for something a bit different.

We support our Site Management Associates with manageable workloads and a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation; bonuses based on performance and great career path. Additionally, we use cutting-edge technology to ensure better outcomes.