Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward!
Proclinical is seeking a Data Quality Lead to oversee the design, implementation, and oversight of data management activities across one or more clinical studies. This role focuses on database setup, data cleaning, query resolution, and vendor oversight, ensuring regulatory compliance and data readiness for analysis. You will play a pivotal role in driving process improvements and delivering high-quality data across the clinical portfolio.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
1. Serve as the core representative for Clinical Data Management on study teams, ensuring deliverables are met.
2. Lead the CDM study team and oversee all build, conduct, and close activities for assigned studies.
3. Implement study conventions, processes, knowledge sharing, and best practices.
4. Actively contribute to EDC system programming and maintenance.
5. Ensure data is analysis-ready by managing data flow from collection to submission.
6. Collaborate with IT to enhance systems through programming (e.g., SQL, SAS, Python).
7. Act as the primary point of contact for CDM leadership in cross-functional settings.
Key Skills and Requirements:
8. Degree in a relevant field (BA/BS or equivalent) with experience in clinical research.
9. Strong understanding of CDM business processes and global regulatory requirements (e.g., GCDMP, ICH-GCP).
10. Proficiency in programming languages such as SQL, SAS, or Python.
11. Proven ability to manage vendors and ensure high-quality database delivery.
12. Excellent communication and presentation skills in English.