Clinical Integration Analyst

OCS Life Sciences; 's-Hertogenbosch; On-site; EUR 60,000 - 90,000; Part time

Benefits offered by this job

24-28 days holiday

Pension scheme

International offices

Job summary

OCS Life Sciences seeks a Clinical Integration Analyst in ‘s-Hertogenbosch to join the Clinical Systems Integration team. The role blends clinical data domain knowledge with system integration and validation to enable data flows and analytics environments rather than performing statistical analysis.

You will stay in close contact with clients to clarify requirements and continually update knowledge on new technologies to deliver the best possible solution.

Qualifications

• 5+ years of CRO biometrics or related roles
• Knowledge of data standards (CDISC, TMF)
• Understanding of pharmaceutical regulation (ICH, GCP, 21 CFR)
• Experience with EDC, eCOA, IWRS
• Scripting languages (Python, Shell)
• Basics of networking protocols (HTTP, FTP)
• Professional proficiency in English

Responsibilities

• Combine clinical data domain knowledge with IT solutions and system integration
• Clarify client requirements and deliver robust analytics-enabled environments

Skills

English proficiency

Self-starter

Prioritization under minimal supervisn

Education

BSc or MSc in Science/Engineering/Life Sciences

Tools

SAS/R

Python

Shell

Job description

Clinical Integration Analyst, 32-40 hours, 's-Hertogenbosch

Expanding our Clinical Systems Integration team

Clinical Systems Integration is a specialized division of OCS Life sciences. This division supports pharmaceutical and CRO clients by building and enhancing their regulated IT systems. Due to increased demand, OCS seeks to expand this team with a Clinical Integration Analyst. This is a cross-functional role combining clinical data domain knowledge with system integration and validation responsibilities. The role focuses on enabling data flows and analytics environments rather than performing statistical analysis.

You stay in close contact with clients to clarify the requirements for their environment and you keep your knowledge of new technologies up to date to deliver the best possible solution.

Your Profile

Our Clinical Integration Analyst has both experience in clinical data analysis and IT solutions. You can be a statistical programmer with experience and interest in the broader IT ecosystem, or alternatively, an IT professional who worked closely with Statistical programming processes.

You bring at least 5 years of experience working at a CRO in Biometrics or adjacent roles like Clinical IT. Further you bring:

• BSc or MSc in the direction of Science, Technology, Engineering, Mathematics, or Life Sciences
• Working knowledge of data standards and frameworks applicable to Biometrics (e.g. CDISC, TMF)
• Demonstrated understanding of the applicable pharmaceutical regulation (ICH, GCP, 21 CFR)
• Understanding of systems upstream (e.g. EDC, eCOA, IWRS) and downstream (e.g. document storage) in relationship to the analytics
• Hands-on knowledge of scripting languages other than SAS/R, e.g. Python, shell
• Understanding of basics of networking protocols, e.g. HTTP, FTP
• You are self starting and able to prioritize under minimal supervision
• Professional proficiency in English

Why Join OCS Consulting?

OCS Consulting has a long-standing partnership with SAS Institute and is a trusted partner for the Life Science industry. We have been named SAS Solution Provider and Partner of the Year multiple times. This not only shows our strong connection to SAS but also the excellence of our consulting team and the quality of our services, which gives you a head start.

We value long-term relationships with staff, clients and partners. All our relationships are based on a partnership model of collaboration, trust and mutual respect. Our employees are vital to our success, and we aim to attract the best people who will stay and grow with us.

What We Offer

• Contract for a year, sight on permanent after (full-time or part-time: 32-36 hours per week)
• Competitive salary, based on your experience
• 24-28 days' holiday, with the option to purchase additional days
• Comprehensive pension scheme, no mandatory employee contribution
• International, collaborative work environment (offices in the Netherlands, Belgium, the UK, and Switzerland)