clinical data associate.

Merck offers for this role:

• Competitive salary
• Culture of Inclusion & Belonging
• Growth & Development
• Flexible & Dynamic Environment

The responsibilities of Clinical data associate role are:

• Υou will support the setup, cleaning, validation, and delivery of clinical trial data - working under the guidance of experienced Data Managers while independently managing your assigned activities.
• You will contribute to eCRF development, edit checks, and data validation specifications, and participate in UAT testing.
• You will perform routine data review, discrepancy management, and query generation, tracking and following up on outstanding queries with sites and vendors.
• You will support SAE and non-CRF data reconciliation, prepare data cleaning reports, and contribute to database lock and study closeout activities.
• You will maintain study files and documentation in line with SOPs, and support audit and inspection readiness across the clinical trial lifecycle.

The qualifications of Clinical data associate  role are:

• Bachelor's degree in Life Sciences, Public Health, Data Science, Pharmacy, or a related field, and bring 5–7 years of experience in Clinical Data Management within pharma, biotech, CRO, or life sciences.
• Hands-on experience with EDC systems such as Medidata Rave, Oracle InForm, or Veeva, and a solid understanding of clinical data flow, eCRF design, and data structures.
• Knowledgeable in ICH GCP guidelines and 21 CFR Part 11 regulatory standards, and apply them consistently in your day-to-day work.
• Strong analytical skills - you spot data discrepancies, identify trends, and escalate risks with accuracy and attention to detail.
• Effective communicator who collaborates confidently with cross-functional teams including Biostatistics, Programming, Operations, and external vendors such as CROs.
• You are organised, adaptable, and able to manage multiple priorities and study deliverables simultaneously without losing focus.
• Proficient in Microsoft Excel; experience with SAS, SQL, or Power BI is a plus.
• You are a fast learner who embraces new technologies and thrives in a dynamic, evolving environment.

5-7 years of experience in Clinical Data Management within a pharmaceutical, biotech, CRO, or lif

If this Clinical Data Associate role sounds appealing to you, we want to hear from you today! Apply online now!

For more information, you can contact with Kyrtzali Foteini at +306948238979 or at fkirtzali@randstad.gr

Please note that for transparency and equity reasons, only those applications made online via our site will be assessed. After the screening of all the CVs received, we will only contact the candidates who meet the requirements of the job to arrange an interview. ​ All applications are considered strictly confidential.