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For our RWE Data Generation Team, we are searching an experience Site Manager, someone with a previous clinical Site experience, who will be able to manage the relationship with Sites in Greece and an additional job country (Ideally, Germany).

If you have a previous clinical experience with visibility on Study Start Up activities and you speak English, Greek and a third European Language (German preferable, other languages will be considered), do not hesitate and apply now for this amazing remote opportunity.

Essential Functions

• May perform site selection, start-up/regulatory, initiation, monitoring and close out visits in accordance with contracted scope of work, using good clinical practices applicable regulations, SOPs and work instructions
• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.  Work collaboratively with other functional groups such as Project Management, Regulatory Start-Up (RSU) and Epidemiology.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.  Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Site Management Lead (SML) and/or line manager.  Execute assigned work efficiently and adhere to project timelines and financial goals.
• Manage the progress of assigned studies by documenting regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters, essential document collection and filing and other required study documentation.
• May provide assistance to less experienced clinical staff, including demonstrating appropriate interactions with sites, documentation and other monitoring activities.

We require:

• At least 2 year of previous clinical experience (ideally as a CTA, CRA, in-house CRA, centralized monitor, Study Coordinator and similar);
• Experience in Study Start Up is mandatory for this role;
• A scientific background, ideally with a MSc. in Life Sciences;
• Fluent in English, Greek and a third EU language;
• Great team-working skills;

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com