**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Senior Clinical Data Associate**:
**Join Us as a Senior Clinical Data Associate - Make an Impact at the Forefront of Innovation**:
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance.
As a **Senior Clinical Data Associate**, you will perform all aspects of the data cleaning process with mínimal supervision in accordance with:
- Good Clinical Practices (GCP)
- Standard Operating Procedures / Work Process Documents (SOPs/WPDs)
Your work will support the assessment of the safety and efficacy of investigational products and/or medical devices.
**What You’ll Do**:
**Clinical Data Management Activities**:
- Support the setup of study activities such as:
- Database design
- Testing of data entry screens
- Data Validation Manual (DVM) creation as required
- Review data listings for accuracy and consistency
- Generate, track, and resolve data clarifications and queries
- Make changes to the clinical database as required
**Subject Matter Expertise & Process Improvement**:
- Contribute to the improvement of data management processes on a global level
- Understand project protocol and DVM requirements
**Reporting & Collaboration**:
- Produce project-specific status reports for management and/or clients on a regular basis
- Provide training and work direction to junior staff as required
- Collaborate with project teams while maintaining high quality standards




**Education & Experience Requirements**:
**Required**:
- Bachelor’s degree or equivalent and relevant formal academic/vocational qualification
**Experience**:
- Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 0 to 2 years
In some cases, an equivalency consisting of a combination of appropriate education, training, and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills & Abilities**:
- Regulatory guidelines
- General SOPs
- Client expectations
Strong attention to detail and numerical skills
- Good written and verbal communication skills
- Good analytical and problem-solving skills
- Ability to maintain a high degree of confidentiality with clinical and proprietary client data
- Strong customer focus and excellent interpersonal skills
- Proven flexibility and adaptability
- Ability to set and meet timelines or negotiate schedule changes in response to project demands
- Knowledge of medical/clinical terminology
- Proven ability in achieving applicable technical competencies per the DM competency grid
**Working Conditions & Environment**:
- Work is performed in an office environment with exposure to electrical office equipment
- Occasional drives to site locations
- Occasional travel both domestic and international
**Why Join Us?**:
When you join Thermo Fisher Scientific, you become part of a global team that values:
- Passion
- Innovation
- Commitment to scientific excellence
You’ll work in an environment where collaboration and development are part of the everyday experience — and where your contributions truly make a difference.

📌 Sr Clinical Data Associate (Nápoles)
🏢 Thermo Fisher Scientific
📍 Nápoles