Clinical Research Assistant

Join Our Team as a Clinical Research Assistant – Start Your Career in Clinical Trials!

Are you a motivated and detail-oriented individual eager to begin your journey in clinical research?

We are looking for a young, enthusiastic Clinical Research Assistant to support our growing team in conducting high-quality pharma projects and clinical trials  at Medicover Integrated Clinical Services Romania. This is a unique opportunity to work alongside experienced professionals in a dynamic, collaborative, and learning-driven environment. If you’re passionate about science, healthcare, and making a real-world impact, we’d love to hear from you!

Medicover Integrated Clinical Services (MICS) is part of Medicover – a leading international healthcare and diagnostic services provider.

Location: Chiajna, Ilfov

Emploement type: office based

Your profile:

• You should be preferably licensed in Life Sciences or Engineering;
• Previous experience in life sciences or clinical trials area is preferable, but not mandatory;
• You should have a positive personality, possessing attention to details, flexibility to support and adjust to multiple type of projects, openness to learn and teamwork skills;
• Good knowledge of English language;
• You should possess the ability to read and interpret documents, write routine reports and correspondence;
• You should possess computer skills (Microsoft Office Applications) are mandatory.

Your responsibilities:

• Support the MICS Coordinators and Project Managers in all activities for the projects conducted by MICS for any of the business lines listed in the introductory section of this document (biological or clinical samples acquisition, registration, coordination, chain of custody, results reporting, quality control, source data collection and verification, etc.);
• Support the MICS Coordinators and Project Managers in evaluating the projects protocols and in preparation of the project specific documentation (project plan, laboratory manual, list of reference intervals for the laboratory parameters, instructions for Healthcare Services Providers/clinical sites and investigators);
• Liaise with other project participants (other MICS units, pharma clients, sponsor, CRO, clinical sites teams, laboratory teams) with regards to the project related activities;
• Liase with other testing laboratories, participating in the project;
• Demonstrate a high standard or work by conducting your activities in accordance with Company Standard Operating Procedures, as well as all applicable regulatory requirements;
• Assist in Coordination/Coordinate the logistic aspects of the project (clinical samples shipments).

Medicover Integrated Clinical Services is a specialised business unit within Medicover Diagnostic Services division with the overarching objective to help bring innovative therapies and diagnostics to the market working with pharmaceuticals. diagnostics, biopharma, biotech companies and CROs throughout the world.

Our goal is to serve the needs of international life science partners wishing to tap into the expertise, professionalism, enthusiasm, and work ethic in Germany and Central Eastern Europe, by providing the utmost quality at a reasonable cost, leveraging flexible and innovative thinking, disciplined management, and significant economies of scale with an attractive cost base.

The MICS business unit benefits from the full complement of all the latest equipment and methodologies employed by Medicover’s Healthcare and Diagnostics divisions and is therefore fully equipped and uniquely capable of taking on any challenge along the full spectrum of clinical development needs of the demanding life sciences, medical and pharmaceutical industry.

Medicover Integrated Clinical Service’s services include and are organised along discrete lines of activity, including: Central Lab Services, Precision Medicine, Biospecimen Sourcing Management and Site Management Organisation.