Clinical Data Associate (all genders)
About this opportunity
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Every breakthrough medicine starts with data - and behind every reliable dataset is someone who cares deeply about getting it right. As a Clinical Data Associate (all genders) within our Data Monitoring, Management & Innovation (DMMI) team, you'll be at the heart of clinical trial execution, ensuring the data that drives life-changing decisions is clean, accurate, and inspection-ready.
This isn't just a data role. It's a role where your precision, curiosity, and collaborative spirit directly contribute to bringing new therapies to patients around the world.
This role requires to be on-site in our office in Maroussi, Greece for 3 days per week.
Your Role:
In your role as Clinical Data Associate (all genders), you 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.
Who You 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
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 303 comparable Associate Clinical Development roles across 61 biopharma companies.
Salary context
78 of 303 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 303 comparable roles
+ 35 more countries
Seniority mix
303 of 303 peers have a known seniority level
Therapeutic area mix
19 of 303 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.